PubMed:2394747 JSONTXT

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    GlyCosmos6-Glycan-Motif-Image

    {"project":"GlyCosmos6-Glycan-Motif-Image","denotations":[{"id":"T1","span":{"begin":614,"end":623},"obj":"Glycan_Motif"}],"attributes":[{"id":"A1","pred":"image","subj":"T1","obj":"https://api.glycosmos.org/wurcs2image/0.10.0/png/binary/G00031MO"}],"text":"Cell type specificity and activation requirements for NFAT-1 (nuclear factor of activated T-cells) transcriptional activity determined by a new method using transgenic mice to assay transcriptional activity of an individual nuclear factor.\nNuclear factor of activated T-cells (NFAT-1) is a transcription factor which is considered to be an important regulator in early T-cell activation. We have developed a system to monitor the transcriptional activity of NFAT-1 at the single cell level in whole animals. The system is based on the use of an oligomerized NFAT-1 binding motif that directs transcription of SV40 T-antigen in transgenic mice. This report represents the first demonstration that a multimerized short binding motif can function appropriately in transgenic mice. NFAT-1 activity had previously been thought to be confined to activated T-lymphocytes upon release of intracellular calcium. By targeting NFAT-1-dependent gene expression in transgenic mice we discovered new sites of NFAT-1 activity. Besides in T-lymphocytes NFAT-1 activity could also be induced in T-lymphocyte-depleted spleen cells and purified B-lymphocytes and requires agents that both release intracellular calcium and activate protein kinase C. A difference in the time course of appearance of NFAT-1 activity between T-lymphocytes and non-T-lymphocytes was revealed. Constitutive expression was observed in a small population of cells in the dermis and some mice have developed skin lesions. Interestingly, the tissue pattern of expression of the NFAT-1 activity resembles the expression pattern described for HIV-LTR/tat transgenic mice (Vogel, J., Hinrichs, S. H., Reynolds, R. K., Luciw, P. A., and Jay, G. (1988) Nature 335, 606-611). This similarity in expression and the fact that NFAT-1 has been shown to bind functional sequences in HIV-LTR suggest a role for NFAT-1 in dermal activation of the HIV-LTR."}

    Glycosmos6-GlycoEpitope

    {"project":"Glycosmos6-GlycoEpitope","denotations":[{"id":"T1","span":{"begin":614,"end":623},"obj":"http://www.glycoepitope.jp/epitopes/EP0020"}],"text":"Cell type specificity and activation requirements for NFAT-1 (nuclear factor of activated T-cells) transcriptional activity determined by a new method using transgenic mice to assay transcriptional activity of an individual nuclear factor.\nNuclear factor of activated T-cells (NFAT-1) is a transcription factor which is considered to be an important regulator in early T-cell activation. We have developed a system to monitor the transcriptional activity of NFAT-1 at the single cell level in whole animals. The system is based on the use of an oligomerized NFAT-1 binding motif that directs transcription of SV40 T-antigen in transgenic mice. This report represents the first demonstration that a multimerized short binding motif can function appropriately in transgenic mice. NFAT-1 activity had previously been thought to be confined to activated T-lymphocytes upon release of intracellular calcium. By targeting NFAT-1-dependent gene expression in transgenic mice we discovered new sites of NFAT-1 activity. Besides in T-lymphocytes NFAT-1 activity could also be induced in T-lymphocyte-depleted spleen cells and purified B-lymphocytes and requires agents that both release intracellular calcium and activate protein kinase C. A difference in the time course of appearance of NFAT-1 activity between T-lymphocytes and non-T-lymphocytes was revealed. Constitutive expression was observed in a small population of cells in the dermis and some mice have developed skin lesions. Interestingly, the tissue pattern of expression of the NFAT-1 activity resembles the expression pattern described for HIV-LTR/tat transgenic mice (Vogel, J., Hinrichs, S. H., Reynolds, R. K., Luciw, P. A., and Jay, G. (1988) Nature 335, 606-611). This similarity in expression and the fact that NFAT-1 has been shown to bind functional sequences in HIV-LTR suggest a role for NFAT-1 in dermal activation of the HIV-LTR."}

    sentences

    {"project":"sentences","denotations":[{"id":"T1","span":{"begin":0,"end":239},"obj":"Sentence"},{"id":"T2","span":{"begin":240,"end":387},"obj":"Sentence"},{"id":"T3","span":{"begin":388,"end":507},"obj":"Sentence"},{"id":"T4","span":{"begin":508,"end":643},"obj":"Sentence"},{"id":"T5","span":{"begin":644,"end":777},"obj":"Sentence"},{"id":"T6","span":{"begin":778,"end":902},"obj":"Sentence"},{"id":"T7","span":{"begin":903,"end":1011},"obj":"Sentence"},{"id":"T8","span":{"begin":1012,"end":1230},"obj":"Sentence"},{"id":"T9","span":{"begin":1231,"end":1353},"obj":"Sentence"},{"id":"T10","span":{"begin":1354,"end":1478},"obj":"Sentence"},{"id":"T11","span":{"begin":1479,"end":1649},"obj":"Sentence"},{"id":"T12","span":{"begin":1650,"end":1666},"obj":"Sentence"},{"id":"T13","span":{"begin":1667,"end":1680},"obj":"Sentence"},{"id":"T14","span":{"begin":1681,"end":1725},"obj":"Sentence"},{"id":"T15","span":{"begin":1726,"end":1898},"obj":"Sentence"},{"id":"T1","span":{"begin":0,"end":239},"obj":"Sentence"},{"id":"T2","span":{"begin":240,"end":387},"obj":"Sentence"},{"id":"T3","span":{"begin":388,"end":507},"obj":"Sentence"},{"id":"T4","span":{"begin":508,"end":643},"obj":"Sentence"},{"id":"T5","span":{"begin":644,"end":777},"obj":"Sentence"},{"id":"T6","span":{"begin":778,"end":902},"obj":"Sentence"},{"id":"T7","span":{"begin":903,"end":1011},"obj":"Sentence"},{"id":"T8","span":{"begin":1012,"end":1230},"obj":"Sentence"},{"id":"T9","span":{"begin":1231,"end":1353},"obj":"Sentence"},{"id":"T10","span":{"begin":1354,"end":1478},"obj":"Sentence"},{"id":"T11","span":{"begin":1479,"end":1649},"obj":"Sentence"},{"id":"T12","span":{"begin":1650,"end":1666},"obj":"Sentence"},{"id":"T13","span":{"begin":1667,"end":1680},"obj":"Sentence"},{"id":"T14","span":{"begin":1681,"end":1725},"obj":"Sentence"},{"id":"T15","span":{"begin":1726,"end":1898},"obj":"Sentence"}],"namespaces":[{"prefix":"_base","uri":"http://pubannotation.org/ontology/tao.owl#"}],"text":"Cell type specificity and activation requirements for NFAT-1 (nuclear factor of activated T-cells) transcriptional activity determined by a new method using transgenic mice to assay transcriptional activity of an individual nuclear factor.\nNuclear factor of activated T-cells (NFAT-1) is a transcription factor which is considered to be an important regulator in early T-cell activation. We have developed a system to monitor the transcriptional activity of NFAT-1 at the single cell level in whole animals. The system is based on the use of an oligomerized NFAT-1 binding motif that directs transcription of SV40 T-antigen in transgenic mice. This report represents the first demonstration that a multimerized short binding motif can function appropriately in transgenic mice. NFAT-1 activity had previously been thought to be confined to activated T-lymphocytes upon release of intracellular calcium. By targeting NFAT-1-dependent gene expression in transgenic mice we discovered new sites of NFAT-1 activity. Besides in T-lymphocytes NFAT-1 activity could also be induced in T-lymphocyte-depleted spleen cells and purified B-lymphocytes and requires agents that both release intracellular calcium and activate protein kinase C. A difference in the time course of appearance of NFAT-1 activity between T-lymphocytes and non-T-lymphocytes was revealed. Constitutive expression was observed in a small population of cells in the dermis and some mice have developed skin lesions. Interestingly, the tissue pattern of expression of the NFAT-1 activity resembles the expression pattern described for HIV-LTR/tat transgenic mice (Vogel, J., Hinrichs, S. H., Reynolds, R. K., Luciw, P. A., and Jay, G. (1988) Nature 335, 606-611). This similarity in expression and the fact that NFAT-1 has been shown to bind functional sequences in HIV-LTR suggest a role for NFAT-1 in dermal activation of the HIV-LTR."}

    GlyCosmos6-Glycan-Motif-Structure

    {"project":"GlyCosmos6-Glycan-Motif-Structure","denotations":[{"id":"T1","span":{"begin":614,"end":623},"obj":"https://glytoucan.org/Structures/Glycans/G00031MO"}],"text":"Cell type specificity and activation requirements for NFAT-1 (nuclear factor of activated T-cells) transcriptional activity determined by a new method using transgenic mice to assay transcriptional activity of an individual nuclear factor.\nNuclear factor of activated T-cells (NFAT-1) is a transcription factor which is considered to be an important regulator in early T-cell activation. We have developed a system to monitor the transcriptional activity of NFAT-1 at the single cell level in whole animals. The system is based on the use of an oligomerized NFAT-1 binding motif that directs transcription of SV40 T-antigen in transgenic mice. This report represents the first demonstration that a multimerized short binding motif can function appropriately in transgenic mice. NFAT-1 activity had previously been thought to be confined to activated T-lymphocytes upon release of intracellular calcium. By targeting NFAT-1-dependent gene expression in transgenic mice we discovered new sites of NFAT-1 activity. Besides in T-lymphocytes NFAT-1 activity could also be induced in T-lymphocyte-depleted spleen cells and purified B-lymphocytes and requires agents that both release intracellular calcium and activate protein kinase C. A difference in the time course of appearance of NFAT-1 activity between T-lymphocytes and non-T-lymphocytes was revealed. Constitutive expression was observed in a small population of cells in the dermis and some mice have developed skin lesions. Interestingly, the tissue pattern of expression of the NFAT-1 activity resembles the expression pattern described for HIV-LTR/tat transgenic mice (Vogel, J., Hinrichs, S. H., Reynolds, R. K., Luciw, P. A., and Jay, G. (1988) Nature 335, 606-611). This similarity in expression and the fact that NFAT-1 has been shown to bind functional sequences in HIV-LTR suggest a role for NFAT-1 in dermal activation of the HIV-LTR."}

    Glycosmos6-MAT

    {"project":"Glycosmos6-MAT","denotations":[{"id":"T1","span":{"begin":1100,"end":1106},"obj":"http://purl.obolibrary.org/obo/MAT_0000085"},{"id":"T2","span":{"begin":1429,"end":1435},"obj":"http://purl.obolibrary.org/obo/MAT_0000153"},{"id":"T3","span":{"begin":1465,"end":1469},"obj":"http://purl.obolibrary.org/obo/MAT_0000284"}],"text":"Cell type specificity and activation requirements for NFAT-1 (nuclear factor of activated T-cells) transcriptional activity determined by a new method using transgenic mice to assay transcriptional activity of an individual nuclear factor.\nNuclear factor of activated T-cells (NFAT-1) is a transcription factor which is considered to be an important regulator in early T-cell activation. We have developed a system to monitor the transcriptional activity of NFAT-1 at the single cell level in whole animals. The system is based on the use of an oligomerized NFAT-1 binding motif that directs transcription of SV40 T-antigen in transgenic mice. This report represents the first demonstration that a multimerized short binding motif can function appropriately in transgenic mice. NFAT-1 activity had previously been thought to be confined to activated T-lymphocytes upon release of intracellular calcium. By targeting NFAT-1-dependent gene expression in transgenic mice we discovered new sites of NFAT-1 activity. Besides in T-lymphocytes NFAT-1 activity could also be induced in T-lymphocyte-depleted spleen cells and purified B-lymphocytes and requires agents that both release intracellular calcium and activate protein kinase C. A difference in the time course of appearance of NFAT-1 activity between T-lymphocytes and non-T-lymphocytes was revealed. Constitutive expression was observed in a small population of cells in the dermis and some mice have developed skin lesions. Interestingly, the tissue pattern of expression of the NFAT-1 activity resembles the expression pattern described for HIV-LTR/tat transgenic mice (Vogel, J., Hinrichs, S. H., Reynolds, R. K., Luciw, P. A., and Jay, G. (1988) Nature 335, 606-611). This similarity in expression and the fact that NFAT-1 has been shown to bind functional sequences in HIV-LTR suggest a role for NFAT-1 in dermal activation of the HIV-LTR."}

    jnlpba-st-training

    {"project":"jnlpba-st-training","denotations":[{"id":"T1","span":{"begin":54,"end":60},"obj":"protein"},{"id":"T2","span":{"begin":62,"end":76},"obj":"protein"},{"id":"T3","span":{"begin":80,"end":97},"obj":"cell_type"},{"id":"T4","span":{"begin":224,"end":238},"obj":"protein"},{"id":"T5","span":{"begin":240,"end":254},"obj":"protein"},{"id":"T6","span":{"begin":258,"end":275},"obj":"cell_type"},{"id":"T7","span":{"begin":277,"end":283},"obj":"protein"},{"id":"T8","span":{"begin":290,"end":310},"obj":"protein"},{"id":"T9","span":{"begin":458,"end":464},"obj":"protein"},{"id":"T10","span":{"begin":558,"end":564},"obj":"protein"},{"id":"T11","span":{"begin":592,"end":623},"obj":"protein"},{"id":"T12","span":{"begin":778,"end":784},"obj":"protein"},{"id":"T13","span":{"begin":840,"end":863},"obj":"cell_type"},{"id":"T14","span":{"begin":880,"end":901},"obj":"cell_type"},{"id":"T15","span":{"begin":916,"end":922},"obj":"protein"},{"id":"T16","span":{"begin":995,"end":1001},"obj":"protein"},{"id":"T17","span":{"begin":1023,"end":1036},"obj":"cell_type"},{"id":"T18","span":{"begin":1037,"end":1043},"obj":"protein"},{"id":"T19","span":{"begin":1078,"end":1112},"obj":"cell_type"},{"id":"T20","span":{"begin":1117,"end":1139},"obj":"cell_type"},{"id":"T21","span":{"begin":1213,"end":1229},"obj":"protein"},{"id":"T22","span":{"begin":1280,"end":1286},"obj":"protein"},{"id":"T23","span":{"begin":1304,"end":1317},"obj":"cell_type"},{"id":"T24","span":{"begin":1322,"end":1339},"obj":"cell_type"},{"id":"T25","span":{"begin":1534,"end":1540},"obj":"protein"},{"id":"T26","span":{"begin":1774,"end":1780},"obj":"protein"},{"id":"T27","span":{"begin":1804,"end":1824},"obj":"DNA"},{"id":"T28","span":{"begin":1828,"end":1835},"obj":"DNA"},{"id":"T29","span":{"begin":1855,"end":1861},"obj":"protein"},{"id":"T30","span":{"begin":1890,"end":1897},"obj":"DNA"}],"text":"Cell type specificity and activation requirements for NFAT-1 (nuclear factor of activated T-cells) transcriptional activity determined by a new method using transgenic mice to assay transcriptional activity of an individual nuclear factor.\nNuclear factor of activated T-cells (NFAT-1) is a transcription factor which is considered to be an important regulator in early T-cell activation. We have developed a system to monitor the transcriptional activity of NFAT-1 at the single cell level in whole animals. The system is based on the use of an oligomerized NFAT-1 binding motif that directs transcription of SV40 T-antigen in transgenic mice. This report represents the first demonstration that a multimerized short binding motif can function appropriately in transgenic mice. NFAT-1 activity had previously been thought to be confined to activated T-lymphocytes upon release of intracellular calcium. By targeting NFAT-1-dependent gene expression in transgenic mice we discovered new sites of NFAT-1 activity. Besides in T-lymphocytes NFAT-1 activity could also be induced in T-lymphocyte-depleted spleen cells and purified B-lymphocytes and requires agents that both release intracellular calcium and activate protein kinase C. A difference in the time course of appearance of NFAT-1 activity between T-lymphocytes and non-T-lymphocytes was revealed. Constitutive expression was observed in a small population of cells in the dermis and some mice have developed skin lesions. Interestingly, the tissue pattern of expression of the NFAT-1 activity resembles the expression pattern described for HIV-LTR/tat transgenic mice (Vogel, J., Hinrichs, S. H., Reynolds, R. K., Luciw, P. A., and Jay, G. (1988) Nature 335, 606-611). This similarity in expression and the fact that NFAT-1 has been shown to bind functional sequences in HIV-LTR suggest a role for NFAT-1 in dermal activation of the HIV-LTR."}

    genia-medco-coref

    {"project":"genia-medco-coref","denotations":[{"id":"C1","span":{"begin":54,"end":123},"obj":"NP"},{"id":"C2","span":{"begin":157,"end":172},"obj":"NP"},{"id":"C3","span":{"begin":240,"end":284},"obj":"NP"},{"id":"C4","span":{"begin":288,"end":310},"obj":"NP"},{"id":"C5","span":{"begin":311,"end":316},"obj":"NP"},{"id":"C7","span":{"begin":458,"end":464},"obj":"NP"},{"id":"C6","span":{"begin":426,"end":464},"obj":"NP"},{"id":"C8","span":{"begin":542,"end":578},"obj":"NP"},{"id":"C9","span":{"begin":579,"end":583},"obj":"NP"},{"id":"C10","span":{"begin":627,"end":642},"obj":"NP"},{"id":"C11","span":{"begin":667,"end":690},"obj":"NP"},{"id":"C12","span":{"begin":691,"end":695},"obj":"NP"},{"id":"C13","span":{"begin":761,"end":776},"obj":"NP"},{"id":"C14","span":{"begin":778,"end":793},"obj":"NP"},{"id":"C15","span":{"begin":880,"end":901},"obj":"NP"},{"id":"C16","span":{"begin":952,"end":967},"obj":"NP"},{"id":"C17","span":{"begin":995,"end":1010},"obj":"NP"},{"id":"C18","span":{"begin":1023,"end":1036},"obj":"NP"},{"id":"C19","span":{"begin":1037,"end":1052},"obj":"NP"},{"id":"C20","span":{"begin":1153,"end":1159},"obj":"NP"},{"id":"C21","span":{"begin":1160,"end":1164},"obj":"NP"},{"id":"C22","span":{"begin":1178,"end":1199},"obj":"NP"},{"id":"C23","span":{"begin":1280,"end":1295},"obj":"NP"},{"id":"C24","span":{"begin":1304,"end":1317},"obj":"NP"},{"id":"C25","span":{"begin":1440,"end":1449},"obj":"NP"},{"id":"C26","span":{"begin":1530,"end":1549},"obj":"NP"},{"id":"C27","span":{"begin":1597,"end":1604},"obj":"NP"},{"id":"C28","span":{"begin":1760,"end":1768},"obj":"NP"},{"id":"C29","span":{"begin":1769,"end":1773},"obj":"NP"},{"id":"C30","span":{"begin":1774,"end":1780},"obj":"NP"},{"id":"C31","span":{"begin":1828,"end":1835},"obj":"NP"},{"id":"C32","span":{"begin":1855,"end":1861},"obj":"NP"},{"id":"C33","span":{"begin":1890,"end":1897},"obj":"NP"}],"relations":[{"id":"R1","pred":"coref-relat","subj":"C5","obj":"C4"},{"id":"R2","pred":"coref-ident","subj":"C7","obj":"C3"},{"id":"R3","pred":"coref-ident","subj":"C6","obj":"C1"},{"id":"R4","pred":"coref-relat","subj":"C9","obj":"C8"},{"id":"R5","pred":"coref-ident","subj":"C10","obj":"C2"},{"id":"R6","pred":"coref-relat","subj":"C12","obj":"C11"},{"id":"R7","pred":"coref-ident","subj":"C13","obj":"C10"},{"id":"R8","pred":"coref-ident","subj":"C14","obj":"C6"},{"id":"R9","pred":"coref-ident","subj":"C16","obj":"C13"},{"id":"R10","pred":"coref-ident","subj":"C17","obj":"C14"},{"id":"R11","pred":"coref-ident","subj":"C19","obj":"C17"},{"id":"R12","pred":"coref-ident","subj":"C21","obj":"C20"},{"id":"R13","pred":"coref-ident","subj":"C22","obj":"C15"},{"id":"R14","pred":"coref-ident","subj":"C23","obj":"C19"},{"id":"R15","pred":"coref-ident","subj":"C24","obj":"C18"},{"id":"R16","pred":"coref-ident","subj":"C25","obj":"C16"},{"id":"R17","pred":"coref-ident","subj":"C26","obj":"C23"},{"id":"R18","pred":"coref-relat","subj":"C29","obj":"C28"},{"id":"R19","pred":"coref-ident","subj":"C30","obj":"C7"},{"id":"R20","pred":"coref-ident","subj":"C31","obj":"C27"},{"id":"R21","pred":"coref-ident","subj":"C32","obj":"C30"},{"id":"R22","pred":"coref-ident","subj":"C33","obj":"C31"}],"text":"Cell type specificity and activation requirements for NFAT-1 (nuclear factor of activated T-cells) transcriptional activity determined by a new method using transgenic mice to assay transcriptional activity of an individual nuclear factor.\nNuclear factor of activated T-cells (NFAT-1) is a transcription factor which is considered to be an important regulator in early T-cell activation. We have developed a system to monitor the transcriptional activity of NFAT-1 at the single cell level in whole animals. The system is based on the use of an oligomerized NFAT-1 binding motif that directs transcription of SV40 T-antigen in transgenic mice. This report represents the first demonstration that a multimerized short binding motif can function appropriately in transgenic mice. NFAT-1 activity had previously been thought to be confined to activated T-lymphocytes upon release of intracellular calcium. By targeting NFAT-1-dependent gene expression in transgenic mice we discovered new sites of NFAT-1 activity. Besides in T-lymphocytes NFAT-1 activity could also be induced in T-lymphocyte-depleted spleen cells and purified B-lymphocytes and requires agents that both release intracellular calcium and activate protein kinase C. A difference in the time course of appearance of NFAT-1 activity between T-lymphocytes and non-T-lymphocytes was revealed. Constitutive expression was observed in a small population of cells in the dermis and some mice have developed skin lesions. Interestingly, the tissue pattern of expression of the NFAT-1 activity resembles the expression pattern described for HIV-LTR/tat transgenic mice (Vogel, J., Hinrichs, S. H., Reynolds, R. K., Luciw, P. A., and Jay, G. (1988) Nature 335, 606-611). This similarity in expression and the fact that NFAT-1 has been shown to bind functional sequences in HIV-LTR suggest a role for NFAT-1 in dermal activation of the HIV-LTR."}

    semrep-sample

    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type specificity and activation requirements for NFAT-1 (nuclear factor of activated T-cells) transcriptional activity determined by a new method using transgenic mice to assay transcriptional activity of an individual nuclear factor.\nNuclear factor of activated T-cells (NFAT-1) is a transcription factor which is considered to be an important regulator in early T-cell activation. We have developed a system to monitor the transcriptional activity of NFAT-1 at the single cell level in whole animals. The system is based on the use of an oligomerized NFAT-1 binding motif that directs transcription of SV40 T-antigen in transgenic mice. This report represents the first demonstration that a multimerized short binding motif can function appropriately in transgenic mice. NFAT-1 activity had previously been thought to be confined to activated T-lymphocytes upon release of intracellular calcium. By targeting NFAT-1-dependent gene expression in transgenic mice we discovered new sites of NFAT-1 activity. Besides in T-lymphocytes NFAT-1 activity could also be induced in T-lymphocyte-depleted spleen cells and purified B-lymphocytes and requires agents that both release intracellular calcium and activate protein kinase C. A difference in the time course of appearance of NFAT-1 activity between T-lymphocytes and non-T-lymphocytes was revealed. Constitutive expression was observed in a small population of cells in the dermis and some mice have developed skin lesions. Interestingly, the tissue pattern of expression of the NFAT-1 activity resembles the expression pattern described for HIV-LTR/tat transgenic mice (Vogel, J., Hinrichs, S. H., Reynolds, R. K., Luciw, P. A., and Jay, G. (1988) Nature 335, 606-611). This similarity in expression and the fact that NFAT-1 has been shown to bind functional sequences in HIV-LTR suggest a role for NFAT-1 in dermal activation of the HIV-LTR."}

    pubmed-sentences-benchmark

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    GENIAcorpus

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We have developed a system to monitor the transcriptional activity of NFAT-1 at the single cell level in whole animals. The system is based on the use of an oligomerized NFAT-1 binding motif that directs transcription of SV40 T-antigen in transgenic mice. This report represents the first demonstration that a multimerized short binding motif can function appropriately in transgenic mice. NFAT-1 activity had previously been thought to be confined to activated T-lymphocytes upon release of intracellular calcium. By targeting NFAT-1-dependent gene expression in transgenic mice we discovered new sites of NFAT-1 activity. Besides in T-lymphocytes NFAT-1 activity could also be induced in T-lymphocyte-depleted spleen cells and purified B-lymphocytes and requires agents that both release intracellular calcium and activate protein kinase C. A difference in the time course of appearance of NFAT-1 activity between T-lymphocytes and non-T-lymphocytes was revealed. Constitutive expression was observed in a small population of cells in the dermis and some mice have developed skin lesions. Interestingly, the tissue pattern of expression of the NFAT-1 activity resembles the expression pattern described for HIV-LTR/tat transgenic mice (Vogel, J., Hinrichs, S. H., Reynolds, R. K., Luciw, P. A., and Jay, G. (1988) Nature 335, 606-611). This similarity in expression and the fact that NFAT-1 has been shown to bind functional sequences in HIV-LTR suggest a role for NFAT-1 in dermal activation of the HIV-LTR."}

    metamap-sample

    {"project":"metamap-sample","denotations":[{"id":"T1","span":{"begin":1610,"end":1625},"obj":"C0025936"},{"id":"T2","span":{"begin":953,"end":968},"obj":"C0025936"},{"id":"T3","span":{"begin":762,"end":777},"obj":"C0025936"},{"id":"T4","span":{"begin":628,"end":643},"obj":"C0025936"},{"id":"T5","span":{"begin":158,"end":173},"obj":"C0025936"},{"id":"T6","span":{"begin":593,"end":606},"obj":"C0040649"},{"id":"T7","span":{"begin":431,"end":446},"obj":"C0040649"},{"id":"T8","span":{"begin":100,"end":115},"obj":"C0040649"},{"id":"T9","span":{"begin":145,"end":151},"obj":"C0025663"},{"id":"T10","span":{"begin":177,"end":182},"obj":"C1510438"},{"id":"T11","span":{"begin":1,"end":10},"obj":"C0449475"},{"id":"T12","span":{"begin":536,"end":542},"obj":"C1524063"},{"id":"T13","span":{"begin":152,"end":156},"obj":"C1524063"},{"id":"T14","span":{"begin":11,"end":22},"obj":"C1511884"},{"id":"T15","span":{"begin":1535,"end":1541},"obj":"C0288011"},{"id":"T16","span":{"begin":1281,"end":1287},"obj":"C0288011"},{"id":"T17","span":{"begin":1038,"end":1044},"obj":"C0288011"},{"id":"T18","span":{"begin":779,"end":785},"obj":"C0288011"},{"id":"T19","span":{"begin":559,"end":565},"obj":"C0288011"},{"id":"T20","span":{"begin":459,"end":465},"obj":"C0288011"},{"id":"T21","span":{"begin":278,"end":284},"obj":"C0288011"},{"id":"T22","span":{"begin":241,"end":276},"obj":"C0288011"},{"id":"T23","span":{"begin":55,"end":61},"obj":"C0288011"},{"id":"T24","span":{"begin":1873,"end":1883},"obj":"C1879547"},{"id":"T25","span":{"begin":27,"end":37},"obj":"C1879547"},{"id":"T26","span":{"begin":38,"end":50},"obj":"C1514873"},{"id":"T27","span":{"begin":1542,"end":1550},"obj":"C1561536"},{"id":"T28","span":{"begin":1288,"end":1296},"obj":"C1561536"},{"id":"T29","span":{"begin":1045,"end":1053},"obj":"C1561536"},{"id":"T30","span":{"begin":1003,"end":1011},"obj":"C1561536"},{"id":"T31","span":{"begin":786,"end":794},"obj":"C1561536"},{"id":"T32","span":{"begin":447,"end":455},"obj":"C1561536"},{"id":"T33","span":{"begin":116,"end":124},"obj":"C1561536"},{"id":"T34","span":{"begin":983,"end":986},"obj":"C0205314"},{"id":"T35","span":{"begin":141,"end":144},"obj":"C0205314"},{"id":"T36","span":{"begin":225,"end":231},"obj":"C0521447"},{"id":"T37","span":{"begin":214,"end":224},"obj":"C0027361"},{"id":"T38","span":{"begin":1079,"end":1091},"obj":"C0039194"},{"id":"T39","span":{"begin":1024,"end":1037},"obj":"C0039194"},{"id":"T40","span":{"begin":1598,"end":1601},"obj":"C0019699"},{"id":"T41","span":{"begin":1602,"end":1605},"obj":"C0023978"},{"id":"T42","span":{"begin":726,"end":731},"obj":"C1514562"},{"id":"T43","span":{"begin":574,"end":579},"obj":"C1514562"},{"id":"T44","span":{"begin":1446,"end":1450},"obj":"C0026809"},{"id":"T45","span":{"begin":1214,"end":1230},"obj":"C0033634"},{"id":"T46","span":{"begin":1193,"end":1200},"obj":"C0006675"},{"id":"T47","span":{"begin":895,"end":902},"obj":"C0006675"},{"id":"T48","span":{"begin":1127,"end":1140},"obj":"C0004561"},{"id":"T49","span":{"begin":1651,"end":1652},"obj":"C0033727"},{"id":"T50","span":{"begin":1816,"end":1825},"obj":"C0162326"},{"id":"T51","span":{"begin":1797,"end":1799},"obj":"C1883351"},{"id":"T52","span":{"begin":823,"end":825},"obj":"C1883351"},{"id":"T53","span":{"begin":332,"end":334},"obj":"C1883351"},{"id":"T54","span":{"begin":736,"end":744},"obj":"C0031843"},{"id":"T55","span":{"begin":1746,"end":1756},"obj":"C0185117"},{"id":"T56","span":{"begin":1368,"end":1378},"obj":"C0185117"},{"id":"T57","span":{"begin":1430,"end":1436},"obj":"C0011646"},{"id":"T58","span":{"begin":291,"end":311},"obj":"C0040648"},{"id":"T59","span":{"begin":815,"end":822},"obj":"C0039869"},{"id":"T60","span":{"begin":1800,"end":1804},"obj":"C1167622"},{"id":"T61","span":{"begin":718,"end":725},"obj":"C1167622"},{"id":"T62","span":{"begin":566,"end":573},"obj":"C1167622"},{"id":"T63","span":{"begin":1171,"end":1178},"obj":"C0439180"},{"id":"T64","span":{"begin":870,"end":877},"obj":"C0439180"},{"id":"T65","span":{"begin":934,"end":949},"obj":"C0017262"},{"id":"T66","span":{"begin":1403,"end":1413},"obj":"C1257890"},{"id":"T67","span":{"begin":513,"end":519},"obj":"C0449913"},{"id":"T68","span":{"begin":409,"end":415},"obj":"C0449913"},{"id":"T69","span":{"begin":1417,"end":1422},"obj":"C0007634"},{"id":"T70","span":{"begin":1108,"end":1113},"obj":"C0007634"},{"id":"T71","span":{"begin":1179,"end":1192},"obj":"C0178719"},{"id":"T72","span":{"begin":881,"end":894},"obj":"C0178719"},{"id":"T73","span":{"begin":585,"end":592},"obj":"C0439851"},{"id":"T74","span":{"begin":1695,"end":1696},"obj":"C0439267"},{"id":"T75","span":{"begin":1690,"end":1693},"obj":"C0326402"},{"id":"T76","span":{"begin":1679,"end":1680},"obj":"C2603361"},{"id":"T77","span":{"begin":419,"end":426},"obj":"C0150369"},{"id":"T78","span":{"begin":650,"end":656},"obj":"C0700287"},{"id":"T79","span":{"begin":657,"end":667},"obj":"C1882932"},{"id":"T80","span":{"begin":1345,"end":1353},"obj":"C0443289"},{"id":"T81","span":{"begin":120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type specificity and activation requirements for NFAT-1 (nuclear factor of activated T-cells) transcriptional activity determined by a new method using transgenic mice to assay transcriptional activity of an individual nuclear factor.\nNuclear factor of activated T-cells (NFAT-1) is a transcription factor which is considered to be an important regulator in early T-cell activation. We have developed a system to monitor the transcriptional activity of NFAT-1 at the single cell level in whole animals. The system is based on the use of an oligomerized NFAT-1 binding motif that directs transcription of SV40 T-antigen in transgenic mice. This report represents the first demonstration that a multimerized short binding motif can function appropriately in transgenic mice. NFAT-1 activity had previously been thought to be confined to activated T-lymphocytes upon release of intracellular calcium. By targeting NFAT-1-dependent gene expression in transgenic mice we discovered new sites of NFAT-1 activity. Besides in T-lymphocytes NFAT-1 activity could also be induced in T-lymphocyte-depleted spleen cells and purified B-lymphocytes and requires agents that both release intracellular calcium and activate protein kinase C. A difference in the time course of appearance of NFAT-1 activity between T-lymphocytes and non-T-lymphocytes was revealed. Constitutive expression was observed in a small population of cells in the dermis and some mice have developed skin lesions. Interestingly, the tissue pattern of expression of the NFAT-1 activity resembles the expression pattern described for HIV-LTR/tat transgenic mice (Vogel, J., Hinrichs, S. H., Reynolds, R. K., Luciw, P. A., and Jay, G. (1988) Nature 335, 606-611). This similarity in expression and the fact that NFAT-1 has been shown to bind functional sequences in HIV-LTR suggest a role for NFAT-1 in dermal activation of the HIV-LTR."}

    GlyCosmos15-Glycan

    {"project":"GlyCosmos15-Glycan","denotations":[{"id":"T1","span":{"begin":614,"end":623},"obj":"Glycan"}],"attributes":[{"id":"A1","pred":"glycosmos_id","subj":"T1","obj":"https://glycosmos.org/glycans/show/G00031MO"},{"id":"A2","pred":"image","subj":"T1","obj":"https://api.glycosmos.org/wurcs2image/latest/png/binary/G00031MO"}],"text":"Cell type specificity and activation requirements for NFAT-1 (nuclear factor of activated T-cells) transcriptional activity determined by a new method using transgenic mice to assay transcriptional activity of an individual nuclear factor.\nNuclear factor of activated T-cells (NFAT-1) is a transcription factor which is considered to be an important regulator in early T-cell activation. We have developed a system to monitor the transcriptional activity of NFAT-1 at the single cell level in whole animals. The system is based on the use of an oligomerized NFAT-1 binding motif that directs transcription of SV40 T-antigen in transgenic mice. This report represents the first demonstration that a multimerized short binding motif can function appropriately in transgenic mice. NFAT-1 activity had previously been thought to be confined to activated T-lymphocytes upon release of intracellular calcium. By targeting NFAT-1-dependent gene expression in transgenic mice we discovered new sites of NFAT-1 activity. Besides in T-lymphocytes NFAT-1 activity could also be induced in T-lymphocyte-depleted spleen cells and purified B-lymphocytes and requires agents that both release intracellular calcium and activate protein kinase C. A difference in the time course of appearance of NFAT-1 activity between T-lymphocytes and non-T-lymphocytes was revealed. Constitutive expression was observed in a small population of cells in the dermis and some mice have developed skin lesions. Interestingly, the tissue pattern of expression of the NFAT-1 activity resembles the expression pattern described for HIV-LTR/tat transgenic mice (Vogel, J., Hinrichs, S. H., Reynolds, R. K., Luciw, P. A., and Jay, G. (1988) Nature 335, 606-611). This similarity in expression and the fact that NFAT-1 has been shown to bind functional sequences in HIV-LTR suggest a role for NFAT-1 in dermal activation of the HIV-LTR."}

    Anatomy-MAT

    {"project":"Anatomy-MAT","denotations":[{"id":"T1","span":{"begin":1100,"end":1106},"obj":"Body_part"},{"id":"T2","span":{"begin":1429,"end":1435},"obj":"Body_part"},{"id":"T3","span":{"begin":1465,"end":1469},"obj":"Body_part"}],"attributes":[{"id":"A1","pred":"mat_id","subj":"T1","obj":"http://purl.obolibrary.org/obo/MAT_0000085"},{"id":"A2","pred":"mat_id","subj":"T2","obj":"http://purl.obolibrary.org/obo/MAT_0000153"},{"id":"A3","pred":"mat_id","subj":"T3","obj":"http://purl.obolibrary.org/obo/MAT_0000284"}],"text":"Cell type specificity and activation requirements for NFAT-1 (nuclear factor of activated T-cells) transcriptional activity determined by a new method using transgenic mice to assay transcriptional activity of an individual nuclear factor.\nNuclear factor of activated T-cells (NFAT-1) is a transcription factor which is considered to be an important regulator in early T-cell activation. We have developed a system to monitor the transcriptional activity of NFAT-1 at the single cell level in whole animals. The system is based on the use of an oligomerized NFAT-1 binding motif that directs transcription of SV40 T-antigen in transgenic mice. This report represents the first demonstration that a multimerized short binding motif can function appropriately in transgenic mice. NFAT-1 activity had previously been thought to be confined to activated T-lymphocytes upon release of intracellular calcium. By targeting NFAT-1-dependent gene expression in transgenic mice we discovered new sites of NFAT-1 activity. Besides in T-lymphocytes NFAT-1 activity could also be induced in T-lymphocyte-depleted spleen cells and purified B-lymphocytes and requires agents that both release intracellular calcium and activate protein kinase C. A difference in the time course of appearance of NFAT-1 activity between T-lymphocytes and non-T-lymphocytes was revealed. Constitutive expression was observed in a small population of cells in the dermis and some mice have developed skin lesions. Interestingly, the tissue pattern of expression of the NFAT-1 activity resembles the expression pattern described for HIV-LTR/tat transgenic mice (Vogel, J., Hinrichs, S. H., Reynolds, R. K., Luciw, P. A., and Jay, G. (1988) Nature 335, 606-611). This similarity in expression and the fact that NFAT-1 has been shown to bind functional sequences in HIV-LTR suggest a role for NFAT-1 in dermal activation of the HIV-LTR."}

    Organism-PubDic

    {"project":"Organism-PubDic","denotations":[{"id":"T1","span":{"begin":168,"end":172},"obj":"Species"},{"id":"T2","span":{"begin":638,"end":642},"obj":"Species"},{"id":"T3","span":{"begin":772,"end":776},"obj":"Species"},{"id":"T4","span":{"begin":963,"end":967},"obj":"Species"},{"id":"T5","span":{"begin":1445,"end":1449},"obj":"Species"},{"id":"T6","span":{"begin":1620,"end":1624},"obj":"Species"}],"attributes":[{"id":"A1","pred":"db_id","subj":"T1","obj":"10088"},{"id":"A2","pred":"db_id","subj":"T2","obj":"10088"},{"id":"A3","pred":"db_id","subj":"T3","obj":"10088"},{"id":"A4","pred":"db_id","subj":"T4","obj":"10088"},{"id":"A5","pred":"db_id","subj":"T5","obj":"10088"},{"id":"A6","pred":"db_id","subj":"T6","obj":"10088"}],"text":"Cell type specificity and activation requirements for NFAT-1 (nuclear factor of activated T-cells) transcriptional activity determined by a new method using transgenic mice to assay transcriptional activity of an individual nuclear factor.\nNuclear factor of activated T-cells (NFAT-1) is a transcription factor which is considered to be an important regulator in early T-cell activation. We have developed a system to monitor the transcriptional activity of NFAT-1 at the single cell level in whole animals. The system is based on the use of an oligomerized NFAT-1 binding motif that directs transcription of SV40 T-antigen in transgenic mice. This report represents the first demonstration that a multimerized short binding motif can function appropriately in transgenic mice. NFAT-1 activity had previously been thought to be confined to activated T-lymphocytes upon release of intracellular calcium. By targeting NFAT-1-dependent gene expression in transgenic mice we discovered new sites of NFAT-1 activity. Besides in T-lymphocytes NFAT-1 activity could also be induced in T-lymphocyte-depleted spleen cells and purified B-lymphocytes and requires agents that both release intracellular calcium and activate protein kinase C. A difference in the time course of appearance of NFAT-1 activity between T-lymphocytes and non-T-lymphocytes was revealed. Constitutive expression was observed in a small population of cells in the dermis and some mice have developed skin lesions. Interestingly, the tissue pattern of expression of the NFAT-1 activity resembles the expression pattern described for HIV-LTR/tat transgenic mice (Vogel, J., Hinrichs, S. H., Reynolds, R. K., Luciw, P. A., and Jay, G. (1988) Nature 335, 606-611). This similarity in expression and the fact that NFAT-1 has been shown to bind functional sequences in HIV-LTR suggest a role for NFAT-1 in dermal activation of the HIV-LTR."}

    Organism-PubTator

    {"project":"Organism-PubTator","denotations":[{"id":"3","span":{"begin":168,"end":172},"obj":"Species"},{"id":"30","span":{"begin":638,"end":642},"obj":"Species"},{"id":"31","span":{"begin":772,"end":776},"obj":"Species"},{"id":"35","span":{"begin":963,"end":967},"obj":"Species"},{"id":"40","span":{"begin":1445,"end":1449},"obj":"Species"},{"id":"43","span":{"begin":1597,"end":1604},"obj":"Species"},{"id":"45","span":{"begin":1620,"end":1624},"obj":"Species"},{"id":"47","span":{"begin":1828,"end":1835},"obj":"Species"},{"id":"49","span":{"begin":1890,"end":1897},"obj":"Species"}],"attributes":[{"id":"A3","pred":"db_id","subj":"3","obj":"10090"},{"id":"A30","pred":"db_id","subj":"30","obj":"10090"},{"id":"A31","pred":"db_id","subj":"31","obj":"10090"},{"id":"A35","pred":"db_id","subj":"35","obj":"10090"},{"id":"A40","pred":"db_id","subj":"40","obj":"10090"},{"id":"A45","pred":"db_id","subj":"45","obj":"10090"}],"text":"Cell type specificity and activation requirements for NFAT-1 (nuclear factor of activated T-cells) transcriptional activity determined by a new method using transgenic mice to assay transcriptional activity of an individual nuclear factor.\nNuclear factor of activated T-cells (NFAT-1) is a transcription factor which is considered to be an important regulator in early T-cell activation. We have developed a system to monitor the transcriptional activity of NFAT-1 at the single cell level in whole animals. The system is based on the use of an oligomerized NFAT-1 binding motif that directs transcription of SV40 T-antigen in transgenic mice. This report represents the first demonstration that a multimerized short binding motif can function appropriately in transgenic mice. NFAT-1 activity had previously been thought to be confined to activated T-lymphocytes upon release of intracellular calcium. By targeting NFAT-1-dependent gene expression in transgenic mice we discovered new sites of NFAT-1 activity. Besides in T-lymphocytes NFAT-1 activity could also be induced in T-lymphocyte-depleted spleen cells and purified B-lymphocytes and requires agents that both release intracellular calcium and activate protein kinase C. A difference in the time course of appearance of NFAT-1 activity between T-lymphocytes and non-T-lymphocytes was revealed. Constitutive expression was observed in a small population of cells in the dermis and some mice have developed skin lesions. Interestingly, the tissue pattern of expression of the NFAT-1 activity resembles the expression pattern described for HIV-LTR/tat transgenic mice (Vogel, J., Hinrichs, S. H., Reynolds, R. K., Luciw, P. A., and Jay, G. (1988) Nature 335, 606-611). This similarity in expression and the fact that NFAT-1 has been shown to bind functional sequences in HIV-LTR suggest a role for NFAT-1 in dermal activation of the HIV-LTR."}

    Organism-PubDic-Bert-9

    {"project":"Organism-PubDic-Bert-9","denotations":[{"id":"T1","span":{"begin":168,"end":172},"obj":"Species"},{"id":"T2","span":{"begin":638,"end":642},"obj":"Species"},{"id":"T3","span":{"begin":772,"end":776},"obj":"Species"},{"id":"T4","span":{"begin":963,"end":967},"obj":"Species"},{"id":"T5","span":{"begin":1445,"end":1449},"obj":"Species"},{"id":"T6","span":{"begin":1620,"end":1624},"obj":"Species"}],"attributes":[{"id":"A1","pred":"db_id","subj":"T1","obj":"10088"},{"id":"A2","pred":"db_id","subj":"T2","obj":"10088"},{"id":"A3","pred":"db_id","subj":"T3","obj":"10088"},{"id":"A4","pred":"db_id","subj":"T4","obj":"10088"},{"id":"A5","pred":"db_id","subj":"T5","obj":"10088"},{"id":"A6","pred":"db_id","subj":"T6","obj":"10088"}],"text":"Cell type specificity and activation requirements for NFAT-1 (nuclear factor of activated T-cells) transcriptional activity determined by a new method using transgenic mice to assay transcriptional activity of an individual nuclear factor.\nNuclear factor of activated T-cells (NFAT-1) is a transcription factor which is considered to be an important regulator in early T-cell activation. We have developed a system to monitor the transcriptional activity of NFAT-1 at the single cell level in whole animals. The system is based on the use of an oligomerized NFAT-1 binding motif that directs transcription of SV40 T-antigen in transgenic mice. This report represents the first demonstration that a multimerized short binding motif can function appropriately in transgenic mice. NFAT-1 activity had previously been thought to be confined to activated T-lymphocytes upon release of intracellular calcium. By targeting NFAT-1-dependent gene expression in transgenic mice we discovered new sites of NFAT-1 activity. Besides in T-lymphocytes NFAT-1 activity could also be induced in T-lymphocyte-depleted spleen cells and purified B-lymphocytes and requires agents that both release intracellular calcium and activate protein kinase C. A difference in the time course of appearance of NFAT-1 activity between T-lymphocytes and non-T-lymphocytes was revealed. Constitutive expression was observed in a small population of cells in the dermis and some mice have developed skin lesions. Interestingly, the tissue pattern of expression of the NFAT-1 activity resembles the expression pattern described for HIV-LTR/tat transgenic mice (Vogel, J., Hinrichs, S. H., Reynolds, R. K., Luciw, P. A., and Jay, G. (1988) Nature 335, 606-611). This similarity in expression and the fact that NFAT-1 has been shown to bind functional sequences in HIV-LTR suggest a role for NFAT-1 in dermal activation of the HIV-LTR."}

    Organism-PubDic-Bert-8

    {"project":"Organism-PubDic-Bert-8","denotations":[{"id":"T1","span":{"begin":168,"end":172},"obj":"Species"},{"id":"T2","span":{"begin":638,"end":642},"obj":"Species"},{"id":"T3","span":{"begin":772,"end":776},"obj":"Species"},{"id":"T4","span":{"begin":963,"end":967},"obj":"Species"},{"id":"T5","span":{"begin":1059,"end":1063},"obj":"Species"},{"id":"T6","span":{"begin":1251,"end":1255},"obj":"Species"},{"id":"T7","span":{"begin":1445,"end":1449},"obj":"Species"},{"id":"T8","span":{"begin":1620,"end":1624},"obj":"Species"},{"id":"T9","span":{"begin":1637,"end":1645},"obj":"Species"},{"id":"T10","span":{"begin":1654,"end":1662},"obj":"Species"},{"id":"T11","span":{"begin":1689,"end":1692},"obj":"Species"}],"attributes":[{"id":"A1","pred":"db_id","subj":"T1","obj":"10088"},{"id":"A2","pred":"db_id","subj":"T2","obj":"10088"},{"id":"A3","pred":"db_id","subj":"T3","obj":"10088"},{"id":"A4","pred":"db_id","subj":"T4","obj":"10088"},{"id":"A5","pred":"db_id","subj":"T5","obj":"209674"},{"id":"A6","pred":"db_id","subj":"T6","obj":"269157"},{"id":"A7","pred":"db_id","subj":"T7","obj":"10088"},{"id":"A8","pred":"db_id","subj":"T8","obj":"10088"},{"id":"A9","pred":"db_id","subj":"T9","obj":"940853"},{"id":"A10","pred":"db_id","subj":"T10","obj":"1292316"},{"id":"A11","pred":"db_id","subj":"T11","obj":"143608"}],"text":"Cell type specificity and activation requirements for NFAT-1 (nuclear factor of activated T-cells) transcriptional activity determined by a new method using transgenic mice to assay transcriptional activity of an individual nuclear factor.\nNuclear factor of activated T-cells (NFAT-1) is a transcription factor which is considered to be an important regulator in early T-cell activation. We have developed a system to monitor the transcriptional activity of NFAT-1 at the single cell level in whole animals. The system is based on the use of an oligomerized NFAT-1 binding motif that directs transcription of SV40 T-antigen in transgenic mice. This report represents the first demonstration that a multimerized short binding motif can function appropriately in transgenic mice. NFAT-1 activity had previously been thought to be confined to activated T-lymphocytes upon release of intracellular calcium. By targeting NFAT-1-dependent gene expression in transgenic mice we discovered new sites of NFAT-1 activity. Besides in T-lymphocytes NFAT-1 activity could also be induced in T-lymphocyte-depleted spleen cells and purified B-lymphocytes and requires agents that both release intracellular calcium and activate protein kinase C. A difference in the time course of appearance of NFAT-1 activity between T-lymphocytes and non-T-lymphocytes was revealed. Constitutive expression was observed in a small population of cells in the dermis and some mice have developed skin lesions. Interestingly, the tissue pattern of expression of the NFAT-1 activity resembles the expression pattern described for HIV-LTR/tat transgenic mice (Vogel, J., Hinrichs, S. H., Reynolds, R. K., Luciw, P. A., and Jay, G. (1988) Nature 335, 606-611). This similarity in expression and the fact that NFAT-1 has been shown to bind functional sequences in HIV-LTR suggest a role for NFAT-1 in dermal activation of the HIV-LTR."}

    Organism-Gold

    {"project":"Organism-Gold","denotations":[{"id":"T1","span":{"begin":168,"end":172},"obj":"Species"},{"id":"T2","span":{"begin":638,"end":642},"obj":"Species"},{"id":"T3","span":{"begin":772,"end":776},"obj":"Species"},{"id":"T4","span":{"begin":963,"end":967},"obj":"Species"},{"id":"T5","span":{"begin":1445,"end":1449},"obj":"Species"},{"id":"T6","span":{"begin":1620,"end":1624},"obj":"Species"}],"attributes":[{"id":"A1","pred":"db_id","subj":"T1","obj":"10088"},{"id":"A2","pred":"db_id","subj":"T2","obj":"10088"},{"id":"A3","pred":"db_id","subj":"T3","obj":"10088"},{"id":"A4","pred":"db_id","subj":"T4","obj":"10088"},{"id":"A5","pred":"db_id","subj":"T5","obj":"10088"},{"id":"A6","pred":"db_id","subj":"T6","obj":"10088"}],"text":"Cell type specificity and activation requirements for NFAT-1 (nuclear factor of activated T-cells) transcriptional activity determined by a new method using transgenic mice to assay transcriptional activity of an individual nuclear factor.\nNuclear factor of activated T-cells (NFAT-1) is a transcription factor which is considered to be an important regulator in early T-cell activation. We have developed a system to monitor the transcriptional activity of NFAT-1 at the single cell level in whole animals. The system is based on the use of an oligomerized NFAT-1 binding motif that directs transcription of SV40 T-antigen in transgenic mice. This report represents the first demonstration that a multimerized short binding motif can function appropriately in transgenic mice. NFAT-1 activity had previously been thought to be confined to activated T-lymphocytes upon release of intracellular calcium. By targeting NFAT-1-dependent gene expression in transgenic mice we discovered new sites of NFAT-1 activity. Besides in T-lymphocytes NFAT-1 activity could also be induced in T-lymphocyte-depleted spleen cells and purified B-lymphocytes and requires agents that both release intracellular calcium and activate protein kinase C. A difference in the time course of appearance of NFAT-1 activity between T-lymphocytes and non-T-lymphocytes was revealed. Constitutive expression was observed in a small population of cells in the dermis and some mice have developed skin lesions. Interestingly, the tissue pattern of expression of the NFAT-1 activity resembles the expression pattern described for HIV-LTR/tat transgenic mice (Vogel, J., Hinrichs, S. H., Reynolds, R. K., Luciw, P. A., and Jay, G. (1988) Nature 335, 606-611). This similarity in expression and the fact that NFAT-1 has been shown to bind functional sequences in HIV-LTR suggest a role for NFAT-1 in dermal activation of the HIV-LTR."}

    GlyCosmos15-Sentences

    {"project":"GlyCosmos15-Sentences","blocks":[{"id":"T1","span":{"begin":0,"end":239},"obj":"Sentence"},{"id":"T2","span":{"begin":240,"end":387},"obj":"Sentence"},{"id":"T3","span":{"begin":388,"end":507},"obj":"Sentence"},{"id":"T4","span":{"begin":508,"end":643},"obj":"Sentence"},{"id":"T5","span":{"begin":644,"end":777},"obj":"Sentence"},{"id":"T6","span":{"begin":778,"end":902},"obj":"Sentence"},{"id":"T7","span":{"begin":903,"end":1011},"obj":"Sentence"},{"id":"T8","span":{"begin":1012,"end":1353},"obj":"Sentence"},{"id":"T9","span":{"begin":1354,"end":1478},"obj":"Sentence"},{"id":"T10","span":{"begin":1479,"end":1725},"obj":"Sentence"},{"id":"T11","span":{"begin":1726,"end":1898},"obj":"Sentence"}],"text":"Cell type specificity and activation requirements for NFAT-1 (nuclear factor of activated T-cells) transcriptional activity determined by a new method using transgenic mice to assay transcriptional activity of an individual nuclear factor.\nNuclear factor of activated T-cells (NFAT-1) is a transcription factor which is considered to be an important regulator in early T-cell activation. We have developed a system to monitor the transcriptional activity of NFAT-1 at the single cell level in whole animals. The system is based on the use of an oligomerized NFAT-1 binding motif that directs transcription of SV40 T-antigen in transgenic mice. This report represents the first demonstration that a multimerized short binding motif can function appropriately in transgenic mice. NFAT-1 activity had previously been thought to be confined to activated T-lymphocytes upon release of intracellular calcium. By targeting NFAT-1-dependent gene expression in transgenic mice we discovered new sites of NFAT-1 activity. Besides in T-lymphocytes NFAT-1 activity could also be induced in T-lymphocyte-depleted spleen cells and purified B-lymphocytes and requires agents that both release intracellular calcium and activate protein kinase C. A difference in the time course of appearance of NFAT-1 activity between T-lymphocytes and non-T-lymphocytes was revealed. Constitutive expression was observed in a small population of cells in the dermis and some mice have developed skin lesions. Interestingly, the tissue pattern of expression of the NFAT-1 activity resembles the expression pattern described for HIV-LTR/tat transgenic mice (Vogel, J., Hinrichs, S. H., Reynolds, R. K., Luciw, P. A., and Jay, G. (1988) Nature 335, 606-611). This similarity in expression and the fact that NFAT-1 has been shown to bind functional sequences in HIV-LTR suggest a role for NFAT-1 in dermal activation of the HIV-LTR."}

    GlyCosmos15-Taxon

    {"project":"GlyCosmos15-Taxon","denotations":[{"id":"T1","span":{"begin":168,"end":172},"obj":"Organism"},{"id":"T2","span":{"begin":638,"end":642},"obj":"Organism"},{"id":"T3","span":{"begin":772,"end":776},"obj":"Organism"},{"id":"T4","span":{"begin":963,"end":967},"obj":"Organism"},{"id":"T5","span":{"begin":1445,"end":1449},"obj":"Organism"},{"id":"T6","span":{"begin":1620,"end":1624},"obj":"Organism"}],"attributes":[{"id":"A1","pred":"db_id","subj":"T1","obj":"10088"},{"id":"A2","pred":"db_id","subj":"T2","obj":"10088"},{"id":"A3","pred":"db_id","subj":"T3","obj":"10088"},{"id":"A4","pred":"db_id","subj":"T4","obj":"10088"},{"id":"A5","pred":"db_id","subj":"T5","obj":"10088"},{"id":"A6","pred":"db_id","subj":"T6","obj":"10088"}],"text":"Cell type specificity and activation requirements for NFAT-1 (nuclear factor of activated T-cells) transcriptional activity determined by a new method using transgenic mice to assay transcriptional activity of an individual nuclear factor.\nNuclear factor of activated T-cells (NFAT-1) is a transcription factor which is considered to be an important regulator in early T-cell activation. We have developed a system to monitor the transcriptional activity of NFAT-1 at the single cell level in whole animals. The system is based on the use of an oligomerized NFAT-1 binding motif that directs transcription of SV40 T-antigen in transgenic mice. This report represents the first demonstration that a multimerized short binding motif can function appropriately in transgenic mice. NFAT-1 activity had previously been thought to be confined to activated T-lymphocytes upon release of intracellular calcium. By targeting NFAT-1-dependent gene expression in transgenic mice we discovered new sites of NFAT-1 activity. Besides in T-lymphocytes NFAT-1 activity could also be induced in T-lymphocyte-depleted spleen cells and purified B-lymphocytes and requires agents that both release intracellular calcium and activate protein kinase C. A difference in the time course of appearance of NFAT-1 activity between T-lymphocytes and non-T-lymphocytes was revealed. Constitutive expression was observed in a small population of cells in the dermis and some mice have developed skin lesions. Interestingly, the tissue pattern of expression of the NFAT-1 activity resembles the expression pattern described for HIV-LTR/tat transgenic mice (Vogel, J., Hinrichs, S. H., Reynolds, R. K., Luciw, P. A., and Jay, G. (1988) Nature 335, 606-611). This similarity in expression and the fact that NFAT-1 has been shown to bind functional sequences in HIV-LTR suggest a role for NFAT-1 in dermal activation of the HIV-LTR."}

    GlyCosmos15-GlycoEpitope

    {"project":"GlyCosmos15-GlycoEpitope","denotations":[{"id":"T1","span":{"begin":614,"end":623},"obj":"http://purl.jp/bio/12/glyco/glycan#Glycan_epitope"}],"attributes":[{"id":"A1","pred":"glycoepitope_id","subj":"T1","obj":"http://www.glycoepitope.jp/epitopes/EP0020"}],"text":"Cell type specificity and activation requirements for NFAT-1 (nuclear factor of activated T-cells) transcriptional activity determined by a new method using transgenic mice to assay transcriptional activity of an individual nuclear factor.\nNuclear factor of activated T-cells (NFAT-1) is a transcription factor which is considered to be an important regulator in early T-cell activation. We have developed a system to monitor the transcriptional activity of NFAT-1 at the single cell level in whole animals. The system is based on the use of an oligomerized NFAT-1 binding motif that directs transcription of SV40 T-antigen in transgenic mice. This report represents the first demonstration that a multimerized short binding motif can function appropriately in transgenic mice. NFAT-1 activity had previously been thought to be confined to activated T-lymphocytes upon release of intracellular calcium. By targeting NFAT-1-dependent gene expression in transgenic mice we discovered new sites of NFAT-1 activity. Besides in T-lymphocytes NFAT-1 activity could also be induced in T-lymphocyte-depleted spleen cells and purified B-lymphocytes and requires agents that both release intracellular calcium and activate protein kinase C. A difference in the time course of appearance of NFAT-1 activity between T-lymphocytes and non-T-lymphocytes was revealed. Constitutive expression was observed in a small population of cells in the dermis and some mice have developed skin lesions. Interestingly, the tissue pattern of expression of the NFAT-1 activity resembles the expression pattern described for HIV-LTR/tat transgenic mice (Vogel, J., Hinrichs, S. H., Reynolds, R. K., Luciw, P. A., and Jay, G. (1988) Nature 335, 606-611). This similarity in expression and the fact that NFAT-1 has been shown to bind functional sequences in HIV-LTR suggest a role for NFAT-1 in dermal activation of the HIV-LTR."}

    GlyCosmos15-UBERON

    {"project":"GlyCosmos15-UBERON","denotations":[{"id":"T1","span":{"begin":369,"end":375},"obj":"Body_part"},{"id":"T2","span":{"begin":850,"end":863},"obj":"Body_part"},{"id":"T3","span":{"begin":880,"end":893},"obj":"Body_part"},{"id":"T4","span":{"begin":1023,"end":1036},"obj":"Body_part"},{"id":"T5","span":{"begin":1078,"end":1090},"obj":"Body_part"},{"id":"T6","span":{"begin":1100,"end":1106},"obj":"Body_part"},{"id":"T7","span":{"begin":1126,"end":1139},"obj":"Body_part"},{"id":"T8","span":{"begin":1178,"end":1191},"obj":"Body_part"},{"id":"T9","span":{"begin":1304,"end":1317},"obj":"Body_part"},{"id":"T10","span":{"begin":1326,"end":1339},"obj":"Body_part"},{"id":"T11","span":{"begin":1429,"end":1435},"obj":"Body_part"},{"id":"T12","span":{"begin":1465,"end":1469},"obj":"Body_part"},{"id":"T16","span":{"begin":1498,"end":1504},"obj":"Body_part"}],"attributes":[{"id":"A1","pred":"uberon_id","subj":"T1","obj":"http://purl.obolibrary.org/obo/CL_0000084"},{"id":"A2","pred":"uberon_id","subj":"T2","obj":"http://purl.obolibrary.org/obo/CL_0000084"},{"id":"A3","pred":"uberon_id","subj":"T3","obj":"http://purl.obolibrary.org/obo/GO_0005622"},{"id":"A4","pred":"uberon_id","subj":"T4","obj":"http://purl.obolibrary.org/obo/CL_0000084"},{"id":"A5","pred":"uberon_id","subj":"T5","obj":"http://purl.obolibrary.org/obo/CL_0000084"},{"id":"A6","pred":"uberon_id","subj":"T6","obj":"http://purl.obolibrary.org/obo/UBERON_0002106"},{"id":"A7","pred":"uberon_id","subj":"T7","obj":"http://purl.obolibrary.org/obo/CL_0000236"},{"id":"A8","pred":"uberon_id","subj":"T8","obj":"http://purl.obolibrary.org/obo/GO_0005622"},{"id":"A9","pred":"uberon_id","subj":"T9","obj":"http://purl.obolibrary.org/obo/CL_0000084"},{"id":"A10","pred":"uberon_id","subj":"T10","obj":"http://purl.obolibrary.org/obo/CL_0000084"},{"id":"A11","pred":"uberon_id","subj":"T11","obj":"http://purl.obolibrary.org/obo/UBERON_0002067"},{"id":"A12","pred":"uberon_id","subj":"T12","obj":"http://purl.obolibrary.org/obo/UBERON_0000014"},{"id":"A13","pred":"uberon_id","subj":"T12","obj":"http://purl.obolibrary.org/obo/UBERON_0001003"},{"id":"A14","pred":"uberon_id","subj":"T12","obj":"http://purl.obolibrary.org/obo/UBERON_0002097"},{"id":"A15","pred":"uberon_id","subj":"T12","obj":"http://purl.obolibrary.org/obo/UBERON_0002199"},{"id":"A16","pred":"uberon_id","subj":"T16","obj":"http://purl.obolibrary.org/obo/UBERON_0000479"}],"text":"Cell type specificity and activation requirements for NFAT-1 (nuclear factor of activated T-cells) transcriptional activity determined by a new method using transgenic mice to assay transcriptional activity of an individual nuclear factor.\nNuclear factor of activated T-cells (NFAT-1) is a transcription factor which is considered to be an important regulator in early T-cell activation. We have developed a system to monitor the transcriptional activity of NFAT-1 at the single cell level in whole animals. The system is based on the use of an oligomerized NFAT-1 binding motif that directs transcription of SV40 T-antigen in transgenic mice. This report represents the first demonstration that a multimerized short binding motif can function appropriately in transgenic mice. NFAT-1 activity had previously been thought to be confined to activated T-lymphocytes upon release of intracellular calcium. By targeting NFAT-1-dependent gene expression in transgenic mice we discovered new sites of NFAT-1 activity. Besides in T-lymphocytes NFAT-1 activity could also be induced in T-lymphocyte-depleted spleen cells and purified B-lymphocytes and requires agents that both release intracellular calcium and activate protein kinase C. A difference in the time course of appearance of NFAT-1 activity between T-lymphocytes and non-T-lymphocytes was revealed. Constitutive expression was observed in a small population of cells in the dermis and some mice have developed skin lesions. Interestingly, the tissue pattern of expression of the NFAT-1 activity resembles the expression pattern described for HIV-LTR/tat transgenic mice (Vogel, J., Hinrichs, S. H., Reynolds, R. K., Luciw, P. A., and Jay, G. (1988) Nature 335, 606-611). This similarity in expression and the fact that NFAT-1 has been shown to bind functional sequences in HIV-LTR suggest a role for NFAT-1 in dermal activation of the HIV-LTR."}

    GlyCosmos15-FMA

    {"project":"GlyCosmos15-FMA","denotations":[{"id":"T1","span":{"begin":850,"end":863},"obj":"Body_part"},{"id":"T2","span":{"begin":1023,"end":1036},"obj":"Body_part"},{"id":"T3","span":{"begin":1078,"end":1090},"obj":"Body_part"},{"id":"T4","span":{"begin":1100,"end":1106},"obj":"Body_part"},{"id":"T5","span":{"begin":1126,"end":1139},"obj":"Body_part"},{"id":"T6","span":{"begin":1304,"end":1317},"obj":"Body_part"},{"id":"T7","span":{"begin":1326,"end":1339},"obj":"Body_part"},{"id":"T8","span":{"begin":1429,"end":1435},"obj":"Body_part"},{"id":"T9","span":{"begin":1465,"end":1469},"obj":"Body_part"},{"id":"T10","span":{"begin":1498,"end":1504},"obj":"Body_part"},{"id":"T11","span":{"begin":1597,"end":1600},"obj":"Body_part"},{"id":"T12","span":{"begin":1828,"end":1831},"obj":"Body_part"},{"id":"T13","span":{"begin":1890,"end":1893},"obj":"Body_part"}],"attributes":[{"id":"A1","pred":"db_id","subj":"T1","obj":"FMA:62870"},{"id":"A2","pred":"db_id","subj":"T2","obj":"FMA:62870"},{"id":"A3","pred":"db_id","subj":"T3","obj":"FMA:62870"},{"id":"A4","pred":"db_id","subj":"T4","obj":"FMA:7196"},{"id":"A5","pred":"db_id","subj":"T5","obj":"FMA:62869"},{"id":"A6","pred":"db_id","subj":"T6","obj":"FMA:62870"},{"id":"A7","pred":"db_id","subj":"T7","obj":"FMA:62870"},{"id":"A8","pred":"db_id","subj":"T8","obj":"FMA:70323"},{"id":"A9","pred":"db_id","subj":"T9","obj":"FMA:7163"},{"id":"A10","pred":"db_id","subj":"T10","obj":"FMA:9637"},{"id":"A11","pred":"db_id","subj":"T11","obj":"FMA:278683"},{"id":"A12","pred":"db_id","subj":"T12","obj":"FMA:278683"},{"id":"A13","pred":"db_id","subj":"T13","obj":"FMA:278683"}],"namespaces":[{"prefix":"FMA","uri":"http://purl.org/sig/ont/fma/fma"}],"text":"Cell type specificity and activation requirements for NFAT-1 (nuclear factor of activated T-cells) transcriptional activity determined by a new method using transgenic mice to assay transcriptional activity of an individual nuclear factor.\nNuclear factor of activated T-cells (NFAT-1) is a transcription factor which is considered to be an important regulator in early T-cell activation. We have developed a system to monitor the transcriptional activity of NFAT-1 at the single cell level in whole animals. The system is based on the use of an oligomerized NFAT-1 binding motif that directs transcription of SV40 T-antigen in transgenic mice. This report represents the first demonstration that a multimerized short binding motif can function appropriately in transgenic mice. NFAT-1 activity had previously been thought to be confined to activated T-lymphocytes upon release of intracellular calcium. By targeting NFAT-1-dependent gene expression in transgenic mice we discovered new sites of NFAT-1 activity. Besides in T-lymphocytes NFAT-1 activity could also be induced in T-lymphocyte-depleted spleen cells and purified B-lymphocytes and requires agents that both release intracellular calcium and activate protein kinase C. A difference in the time course of appearance of NFAT-1 activity between T-lymphocytes and non-T-lymphocytes was revealed. Constitutive expression was observed in a small population of cells in the dermis and some mice have developed skin lesions. Interestingly, the tissue pattern of expression of the NFAT-1 activity resembles the expression pattern described for HIV-LTR/tat transgenic mice (Vogel, J., Hinrichs, S. H., Reynolds, R. K., Luciw, P. A., and Jay, G. (1988) Nature 335, 606-611). This similarity in expression and the fact that NFAT-1 has been shown to bind functional sequences in HIV-LTR suggest a role for NFAT-1 in dermal activation of the HIV-LTR."}

    GlyCosmos15-MAT

    {"project":"GlyCosmos15-MAT","denotations":[{"id":"T1","span":{"begin":1100,"end":1106},"obj":"Body_part"},{"id":"T2","span":{"begin":1429,"end":1435},"obj":"Body_part"},{"id":"T3","span":{"begin":1465,"end":1469},"obj":"Body_part"}],"attributes":[{"id":"A1","pred":"mat_id","subj":"T1","obj":"http://purl.obolibrary.org/obo/MAT_0000085"},{"id":"A2","pred":"mat_id","subj":"T2","obj":"http://purl.obolibrary.org/obo/MAT_0000153"},{"id":"A3","pred":"mat_id","subj":"T3","obj":"http://purl.obolibrary.org/obo/MAT_0000284"}],"text":"Cell type specificity and activation requirements for NFAT-1 (nuclear factor of activated T-cells) transcriptional activity determined by a new method using transgenic mice to assay transcriptional activity of an individual nuclear factor.\nNuclear factor of activated T-cells (NFAT-1) is a transcription factor which is considered to be an important regulator in early T-cell activation. We have developed a system to monitor the transcriptional activity of NFAT-1 at the single cell level in whole animals. The system is based on the use of an oligomerized NFAT-1 binding motif that directs transcription of SV40 T-antigen in transgenic mice. This report represents the first demonstration that a multimerized short binding motif can function appropriately in transgenic mice. NFAT-1 activity had previously been thought to be confined to activated T-lymphocytes upon release of intracellular calcium. By targeting NFAT-1-dependent gene expression in transgenic mice we discovered new sites of NFAT-1 activity. Besides in T-lymphocytes NFAT-1 activity could also be induced in T-lymphocyte-depleted spleen cells and purified B-lymphocytes and requires agents that both release intracellular calcium and activate protein kinase C. A difference in the time course of appearance of NFAT-1 activity between T-lymphocytes and non-T-lymphocytes was revealed. Constitutive expression was observed in a small population of cells in the dermis and some mice have developed skin lesions. Interestingly, the tissue pattern of expression of the NFAT-1 activity resembles the expression pattern described for HIV-LTR/tat transgenic mice (Vogel, J., Hinrichs, S. H., Reynolds, R. K., Luciw, P. A., and Jay, G. (1988) Nature 335, 606-611). This similarity in expression and the fact that NFAT-1 has been shown to bind functional sequences in HIV-LTR suggest a role for NFAT-1 in dermal activation of the HIV-LTR."}

    NCBITAXON

    {"project":"NCBITAXON","denotations":[{"id":"T1","span":{"begin":168,"end":172},"obj":"OrganismTaxon"},{"id":"T2","span":{"begin":638,"end":642},"obj":"OrganismTaxon"},{"id":"T3","span":{"begin":772,"end":776},"obj":"OrganismTaxon"},{"id":"T4","span":{"begin":963,"end":967},"obj":"OrganismTaxon"},{"id":"T5","span":{"begin":1445,"end":1449},"obj":"OrganismTaxon"},{"id":"T6","span":{"begin":1620,"end":1624},"obj":"OrganismTaxon"}],"attributes":[{"id":"A1","pred":"db_id","subj":"T1","obj":"10088"},{"id":"A2","pred":"db_id","subj":"T2","obj":"10088"},{"id":"A3","pred":"db_id","subj":"T3","obj":"10088"},{"id":"A4","pred":"db_id","subj":"T4","obj":"10088"},{"id":"A5","pred":"db_id","subj":"T5","obj":"10088"},{"id":"A6","pred":"db_id","subj":"T6","obj":"10088"}],"text":"Cell type specificity and activation requirements for NFAT-1 (nuclear factor of activated T-cells) transcriptional activity determined by a new method using transgenic mice to assay transcriptional activity of an individual nuclear factor.\nNuclear factor of activated T-cells (NFAT-1) is a transcription factor which is considered to be an important regulator in early T-cell activation. We have developed a system to monitor the transcriptional activity of NFAT-1 at the single cell level in whole animals. The system is based on the use of an oligomerized NFAT-1 binding motif that directs transcription of SV40 T-antigen in transgenic mice. This report represents the first demonstration that a multimerized short binding motif can function appropriately in transgenic mice. NFAT-1 activity had previously been thought to be confined to activated T-lymphocytes upon release of intracellular calcium. By targeting NFAT-1-dependent gene expression in transgenic mice we discovered new sites of NFAT-1 activity. Besides in T-lymphocytes NFAT-1 activity could also be induced in T-lymphocyte-depleted spleen cells and purified B-lymphocytes and requires agents that both release intracellular calcium and activate protein kinase C. A difference in the time course of appearance of NFAT-1 activity between T-lymphocytes and non-T-lymphocytes was revealed. Constitutive expression was observed in a small population of cells in the dermis and some mice have developed skin lesions. Interestingly, the tissue pattern of expression of the NFAT-1 activity resembles the expression pattern described for HIV-LTR/tat transgenic mice (Vogel, J., Hinrichs, S. H., Reynolds, R. K., Luciw, P. A., and Jay, G. (1988) Nature 335, 606-611). This similarity in expression and the fact that NFAT-1 has been shown to bind functional sequences in HIV-LTR suggest a role for NFAT-1 in dermal activation of the HIV-LTR."}

    Anatomy-UBERON

    {"project":"Anatomy-UBERON","denotations":[{"id":"T1","span":{"begin":369,"end":375},"obj":"Body_part"},{"id":"T2","span":{"begin":850,"end":863},"obj":"Body_part"},{"id":"T3","span":{"begin":880,"end":893},"obj":"Body_part"},{"id":"T4","span":{"begin":1023,"end":1036},"obj":"Body_part"},{"id":"T5","span":{"begin":1078,"end":1090},"obj":"Body_part"},{"id":"T6","span":{"begin":1100,"end":1106},"obj":"Body_part"},{"id":"T7","span":{"begin":1126,"end":1139},"obj":"Body_part"},{"id":"T8","span":{"begin":1178,"end":1191},"obj":"Body_part"},{"id":"T9","span":{"begin":1304,"end":1317},"obj":"Body_part"},{"id":"T10","span":{"begin":1326,"end":1339},"obj":"Body_part"},{"id":"T11","span":{"begin":1429,"end":1435},"obj":"Body_part"},{"id":"T12","span":{"begin":1465,"end":1469},"obj":"Body_part"},{"id":"T16","span":{"begin":1498,"end":1504},"obj":"Body_part"}],"attributes":[{"id":"A1","pred":"uberon_id","subj":"T1","obj":"http://purl.obolibrary.org/obo/CL_0000084"},{"id":"A2","pred":"uberon_id","subj":"T2","obj":"http://purl.obolibrary.org/obo/CL_0000084"},{"id":"A3","pred":"uberon_id","subj":"T3","obj":"http://purl.obolibrary.org/obo/GO_0005622"},{"id":"A4","pred":"uberon_id","subj":"T4","obj":"http://purl.obolibrary.org/obo/CL_0000084"},{"id":"A5","pred":"uberon_id","subj":"T5","obj":"http://purl.obolibrary.org/obo/CL_0000084"},{"id":"A6","pred":"uberon_id","subj":"T6","obj":"http://purl.obolibrary.org/obo/UBERON_0002106"},{"id":"A7","pred":"uberon_id","subj":"T7","obj":"http://purl.obolibrary.org/obo/CL_0000236"},{"id":"A8","pred":"uberon_id","subj":"T8","obj":"http://purl.obolibrary.org/obo/GO_0005622"},{"id":"A9","pred":"uberon_id","subj":"T9","obj":"http://purl.obolibrary.org/obo/CL_0000084"},{"id":"A10","pred":"uberon_id","subj":"T10","obj":"http://purl.obolibrary.org/obo/CL_0000084"},{"id":"A11","pred":"uberon_id","subj":"T11","obj":"http://purl.obolibrary.org/obo/UBERON_0002067"},{"id":"A12","pred":"uberon_id","subj":"T12","obj":"http://purl.obolibrary.org/obo/UBERON_0000014"},{"id":"A13","pred":"uberon_id","subj":"T12","obj":"http://purl.obolibrary.org/obo/UBERON_0001003"},{"id":"A14","pred":"uberon_id","subj":"T12","obj":"http://purl.obolibrary.org/obo/UBERON_0002097"},{"id":"A15","pred":"uberon_id","subj":"T12","obj":"http://purl.obolibrary.org/obo/UBERON_0002199"},{"id":"A16","pred":"uberon_id","subj":"T16","obj":"http://purl.obolibrary.org/obo/UBERON_0000479"}],"text":"Cell type specificity and activation requirements for NFAT-1 (nuclear factor of activated T-cells) transcriptional activity determined by a new method using transgenic mice to assay transcriptional activity of an individual nuclear factor.\nNuclear factor of activated T-cells (NFAT-1) is a transcription factor which is considered to be an important regulator in early T-cell activation. We have developed a system to monitor the transcriptional activity of NFAT-1 at the single cell level in whole animals. The system is based on the use of an oligomerized NFAT-1 binding motif that directs transcription of SV40 T-antigen in transgenic mice. This report represents the first demonstration that a multimerized short binding motif can function appropriately in transgenic mice. NFAT-1 activity had previously been thought to be confined to activated T-lymphocytes upon release of intracellular calcium. By targeting NFAT-1-dependent gene expression in transgenic mice we discovered new sites of NFAT-1 activity. Besides in T-lymphocytes NFAT-1 activity could also be induced in T-lymphocyte-depleted spleen cells and purified B-lymphocytes and requires agents that both release intracellular calcium and activate protein kinase C. A difference in the time course of appearance of NFAT-1 activity between T-lymphocytes and non-T-lymphocytes was revealed. Constitutive expression was observed in a small population of cells in the dermis and some mice have developed skin lesions. Interestingly, the tissue pattern of expression of the NFAT-1 activity resembles the expression pattern described for HIV-LTR/tat transgenic mice (Vogel, J., Hinrichs, S. H., Reynolds, R. K., Luciw, P. A., and Jay, G. (1988) Nature 335, 606-611). This similarity in expression and the fact that NFAT-1 has been shown to bind functional sequences in HIV-LTR suggest a role for NFAT-1 in dermal activation of the HIV-LTR."}

    CL-cell

    {"project":"CL-cell","denotations":[{"id":"T1","span":{"begin":90,"end":97},"obj":"Cell"},{"id":"T2","span":{"begin":268,"end":275},"obj":"Cell"},{"id":"T3","span":{"begin":369,"end":375},"obj":"Cell"},{"id":"T4","span":{"begin":850,"end":863},"obj":"Cell"},{"id":"T5","span":{"begin":1023,"end":1036},"obj":"Cell"},{"id":"T6","span":{"begin":1078,"end":1090},"obj":"Cell"},{"id":"T7","span":{"begin":1080,"end":1090},"obj":"Cell"},{"id":"T8","span":{"begin":1126,"end":1139},"obj":"Cell"},{"id":"T9","span":{"begin":1304,"end":1317},"obj":"Cell"},{"id":"T10","span":{"begin":1326,"end":1339},"obj":"Cell"}],"attributes":[{"id":"A1","pred":"cl_id","subj":"T1","obj":"http://purl.obolibrary.org/obo/CL:0000084"},{"id":"A2","pred":"cl_id","subj":"T2","obj":"http://purl.obolibrary.org/obo/CL:0000084"},{"id":"A3","pred":"cl_id","subj":"T3","obj":"http://purl.obolibrary.org/obo/CL:0000084"},{"id":"A4","pred":"cl_id","subj":"T4","obj":"http://purl.obolibrary.org/obo/CL:0000084"},{"id":"A5","pred":"cl_id","subj":"T5","obj":"http://purl.obolibrary.org/obo/CL:0000084"},{"id":"A6","pred":"cl_id","subj":"T6","obj":"http://purl.obolibrary.org/obo/CL:0000084"},{"id":"A7","pred":"cl_id","subj":"T7","obj":"http://purl.obolibrary.org/obo/CL:0000542"},{"id":"A8","pred":"cl_id","subj":"T8","obj":"http://purl.obolibrary.org/obo/CL:0000236"},{"id":"A9","pred":"cl_id","subj":"T9","obj":"http://purl.obolibrary.org/obo/CL:0000084"},{"id":"A10","pred":"cl_id","subj":"T10","obj":"http://purl.obolibrary.org/obo/CL:0000084"}],"text":"Cell type specificity and activation requirements for NFAT-1 (nuclear factor of activated T-cells) transcriptional activity determined by a new method using transgenic mice to assay transcriptional activity of an individual nuclear factor.\nNuclear factor of activated T-cells (NFAT-1) is a transcription factor which is considered to be an important regulator in early T-cell activation. We have developed a system to monitor the transcriptional activity of NFAT-1 at the single cell level in whole animals. The system is based on the use of an oligomerized NFAT-1 binding motif that directs transcription of SV40 T-antigen in transgenic mice. This report represents the first demonstration that a multimerized short binding motif can function appropriately in transgenic mice. NFAT-1 activity had previously been thought to be confined to activated T-lymphocytes upon release of intracellular calcium. By targeting NFAT-1-dependent gene expression in transgenic mice we discovered new sites of NFAT-1 activity. Besides in T-lymphocytes NFAT-1 activity could also be induced in T-lymphocyte-depleted spleen cells and purified B-lymphocytes and requires agents that both release intracellular calcium and activate protein kinase C. A difference in the time course of appearance of NFAT-1 activity between T-lymphocytes and non-T-lymphocytes was revealed. Constitutive expression was observed in a small population of cells in the dermis and some mice have developed skin lesions. Interestingly, the tissue pattern of expression of the NFAT-1 activity resembles the expression pattern described for HIV-LTR/tat transgenic mice (Vogel, J., Hinrichs, S. H., Reynolds, R. K., Luciw, P. A., and Jay, G. (1988) Nature 335, 606-611). This similarity in expression and the fact that NFAT-1 has been shown to bind functional sequences in HIV-LTR suggest a role for NFAT-1 in dermal activation of the HIV-LTR."}