
PubMed:10196196
Annnotations
sentences
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 0-137 | Sentence | denotes | SPI-B activates transcription via a unique proline, serine, and threonine domain and exhibits DNA binding affinity differences from PU.1. |
T2 | 138-252 | Sentence | denotes | SPI-B is a B lymphocyte-specific Ets transcription factor that shares a high degree of similarity with PU.1/SPI-1. |
T3 | 253-437 | Sentence | denotes | In direct contrast to PU.1(-/-) mice that die in utero and lack monocytes, neutrophils, B cells, and T cells, Spi-B-/- mice are viable and exhibit a severe B cell proliferation defect. |
T4 | 438-620 | Sentence | denotes | Since PU.1 is expressed at wild type levels in Spi-B-/- B cells, the mutant mice provide genetic evidence that SPI-B and PU.1 have at least some non-redundant roles in B lymphocytes. |
T5 | 621-757 | Sentence | denotes | To begin to understand the molecular basis for these defects, we delineated functional domains of SPI-B for comparison to those of PU.1. |
T6 | 758-887 | Sentence | denotes | By using a heterologous co-transfection system, we identified two independent transactivation domains in the N terminus of SPI-B. |
T7 | 888-1100 | Sentence | denotes | Interestingly, only one of these domains (amino acids 31-61), a proline/serine/threonine-rich region, unique among Ets proteins, is necessary for transactivation of the immunoglobulin lambda light chain enhancer. |
T8 | 1101-1208 | Sentence | denotes | This transactivation motif is in marked contrast to PU.1, which contains acidic and glutamine-rich domains. |
T9 | 1209-1339 | Sentence | denotes | In addition, we describe a functional PU.1 site within the c-FES promoter which SPI-B fails to bind efficiently and transactivate. |
T10 | 1340-1497 | Sentence | denotes | Finally, we show that SPI-B interacts with the PU.1 cofactors Pip, TBP, c-Jun and with lower affinity to nuclear factor interleukin-6beta and retinoblastoma. |
T11 | 1498-1654 | Sentence | denotes | Taken together, these data suggest that SPI-B binds DNA with a different affinity for certain sites than PU.1 and harbors different transactivation domains. |
T12 | 1655-1797 | Sentence | denotes | We conclude that SPI-B may activate unique target genes in B lymphocytes and interact with unique, although currently unidentified, cofactors. |
relna
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 0-5 | DNA | denotes | SPI-B |
T2 | 132-136 | DNA | denotes | PU.1 |
T3 | 138-143 | DNA | denotes | SPI-B |
T4 | 241-245 | DNA | denotes | PU.1 |
T5 | 246-251 | DNA | denotes | SPI-1 |
T6 | 275-279 | DNA | denotes | PU.1 |
T7 | 363-368 | DNA | denotes | Spi-B |
T8 | 444-448 | DNA | denotes | PU.1 |
T9 | 549-554 | DNA | denotes | SPI-B |
T10 | 559-563 | DNA | denotes | PU.1 |
T11 | 719-724 | DNA | denotes | SPI-B |
T12 | 752-756 | DNA | denotes | PU.1 |
T13 | 881-886 | DNA | denotes | SPI-B |
T14 | 1153-1157 | DNA | denotes | PU.1 |
T15 | 1247-1251 | DNA | denotes | PU.1 |
T16 | 1268-1273 | Protein | denotes | c-FES |
T17 | 1289-1294 | DNA | denotes | SPI-B |
T18 | 1362-1367 | DNA | denotes | SPI-B |
T19 | 1387-1391 | DNA | denotes | PU.1 |
T20 | 1402-1405 | Protein | denotes | Pip |
T21 | 1407-1410 | DNA | denotes | TBP |
T22 | 1412-1417 | DNA | denotes | c-Jun |
T23 | 1538-1543 | DNA | denotes | SPI-B |
T24 | 1603-1607 | DNA | denotes | PU.1 |
T25 | 1672-1677 | DNA | denotes | SPI-B |
R0 | T18 | T20 | linked | SPI-B,Pip |
PubmedHPO
Id | Subject | Object | Predicate | Lexical cue |
---|---|---|---|---|
T1 | 1482-1496 | HP_0009919 | denotes | retinoblastoma |
HP-phenotype
Id | Subject | Object | Predicate | Lexical cue | hp_id |
---|---|---|---|---|---|
T1 | 1482-1496 | Phenotype | denotes | retinoblastoma | HP:0009919 |
mondo_disease
Id | Subject | Object | Predicate | Lexical cue | mondo_id |
---|---|---|---|---|---|
T1 | 1482-1496 | Disease | denotes | retinoblastoma | http://purl.obolibrary.org/obo/MONDO_0008380 |
NCBITAXON
Id | Subject | Object | Predicate | Lexical cue | db_id |
---|---|---|---|---|---|
T1 | 285-289 | OrganismTaxon | denotes | mice | 10088 |
T2 | 372-376 | OrganismTaxon | denotes | mice | 10088 |
T3 | 514-518 | OrganismTaxon | denotes | mice | 10088 |
Anatomy-UBERON
Id | Subject | Object | Predicate | Lexical cue | uberon_id |
---|---|---|---|---|---|
T1 | 149-161 | Body_part | denotes | B lymphocyte | http://purl.obolibrary.org/obo/CL_0000236 |
T2 | 317-326 | Body_part | denotes | monocytes | http://purl.obolibrary.org/obo/CL_0000576|http://purl.obolibrary.org/obo/CL_0001054 |
T4 | 328-339 | Body_part | denotes | neutrophils | http://purl.obolibrary.org/obo/CL_0000775 |
T5 | 409-415 | Body_part | denotes | B cell | http://purl.obolibrary.org/obo/CL_0000236 |
T6 | 606-619 | Body_part | denotes | B lymphocytes | http://purl.obolibrary.org/obo/CL_0000236 |
T7 | 1072-1078 | Body_part | denotes | lambda | http://purl.obolibrary.org/obo/UBERON_0013424 |
T8 | 1714-1727 | Body_part | denotes | B lymphocytes | http://purl.obolibrary.org/obo/CL_0000236 |
CL-cell
Id | Subject | Object | Predicate | Lexical cue | cl_id |
---|---|---|---|---|---|
T1 | 149-161 | Cell | denotes | B lymphocyte | http://purl.obolibrary.org/obo/CL:0000236 |
T2 | 151-161 | Cell | denotes | lymphocyte | http://purl.obolibrary.org/obo/CL:0000542 |
T3 | 317-326 | Cell | denotes | monocytes | http://purl.obolibrary.org/obo/CL:0000576|http://purl.obolibrary.org/obo/CL:0001054 |
T5 | 328-339 | Cell | denotes | neutrophils | http://purl.obolibrary.org/obo/CL:0000775 |
T6 | 341-348 | Cell | denotes | B cells | http://purl.obolibrary.org/obo/CL:0000236 |
T7 | 354-361 | Cell | denotes | T cells | http://purl.obolibrary.org/obo/CL:0000084 |
T8 | 409-415 | Cell | denotes | B cell | http://purl.obolibrary.org/obo/CL:0000236 |
T9 | 494-501 | Cell | denotes | B cells | http://purl.obolibrary.org/obo/CL:0000236 |
T10 | 606-619 | Cell | denotes | B lymphocytes | http://purl.obolibrary.org/obo/CL:0000236 |
T11 | 1714-1727 | Cell | denotes | B lymphocytes | http://purl.obolibrary.org/obo/CL:0000236 |