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:"R2177","pred":"dobj","subj":"T3042","obj":"T3040"},{"id":"R2178","pred":"compound","subj":"T3043","obj":"T3042"},{"id":"R2179","pred":"punct","subj":"T3044","obj":"T3040"},{"id":"R2180","pred":"cc","subj":"T3045","obj":"T3040"},{"id":"R2181","pred":"advmod","subj":"T3046","obj":"T3047"},{"id":"R2182","pred":"conj","subj":"T3047","obj":"T3040"},{"id":"R2183","pred":"det","subj":"T3048","obj":"T3049"},{"id":"R2184","pred":"dobj","subj":"T3049","obj":"T3047"},{"id":"R2185","pred":"punct","subj":"T3050","obj":"T3035"}],"text":"Conclusions\nFrom these observations we conclude that the blue-shifted ECFP, and the red-shifted EYFP variants of wtGFP are both amenable to use in mice. Also since we have established lines of viable and fertile mice having widespread FP expression we have demonstrated that ECFP and EYFP represent developmentally neutral reporters. Since we were unable to obtain ES cells, embryos or mice with widespread expression of a RFP (DsRed1) we conclude that this reporter is not developmentally neutral or that its expression cannot be sustained at levels high enough for detection, and as such is not as versatile as other gene-based fluorescent reporters.\nECFP and EYFP can be distinguished on the basis of their unique non-overlapping spectral profiles, and chimeras comprised of ECFP and EYFP tagged compartments demonstrate that the two reporters can be simultaneously non-invasively visualized within the same embryo or adult organ. Therefore it should be possible to use flow cytometry to isolate cells expressing either or both of the reporters from embryos or adult organs [14].\nThese two reporters can also be used to create pairs of donors and acceptors for in vivo fluorescence energy transfer (FRET) [15]. Since the emission profiles of ECFP and EYFP are the least overlapping of all the usable GFP variants, these ECFP and EYFP currently represent the best combination for co-visualization and for use in multi-spectral double-tagged transgenic, chimeric and/or in vivo FRET experiments (reviewed in [16]).\nThese experiments have demonstrated the feasibility of monitoring multiple FP reporters non-invasively within a single animal, and have shown the developmental neutrality of the FP reporters employed. This should pave the way for novel strategies designed to incorporate the use of compound transgenics or tissue recombination or chimeric analyses where several compartments are to be tagged. This technology should provide new possibilities in manipulating the mouse genome, and non-invasively studying the consequences."}

{"project":"craft-ca-core-ex-dev","denotations":[{"id":"T2664","span":{"begin":101,"end":109},"obj":"SO_EXT:sequence_variant_entity"},{"id":"T2665","span":{"begin":147,"end":151},"obj":"NCBITaxon:10088"},{"id":"T2666","span":{"begin":212,"end":216},"obj":"NCBITaxon:10088"},{"id":"T2667","span":{"begin":238,"end":248},"obj":"GO:0010467"},{"id":"T2668","span":{"begin":365,"end":373},"obj":"CL:0002322"},{"id":"T2669","span":{"begin":368,"end":373},"obj":"CL_GO_EXT:cell"},{"id":"T2670","span":{"begin":375,"end":382},"obj":"UBERON:0000922"},{"id":"T2671","span":{"begin":386,"end":390},"obj":"NCBITaxon:10088"},{"id":"T2672","span":{"begin":407,"end":417},"obj":"GO:0010467"},{"id":"T2673","span":{"begin":510,"end":520},"obj":"GO:0010467"},{"id":"T2674","span":{"begin":619,"end":623},"obj":"SO_EXT:0000704"},{"id":"T2675","span":{"begin":792,"end":798},"obj":"CHEBI_SO_EXT:molecular_label_or_mark_or_tag_process"},{"id":"T2676","span":{"begin":911,"end":917},"obj":"UBERON:0000922"},{"id":"T2677","span":{"begin":921,"end":926},"obj":"UBERON:0007023"},{"id":"T2678","span":{"begin":927,"end":932},"obj":"UBERON:0000062"},{"id":"T2679","span":{"begin":999,"end":1004},"obj":"CL_GO_EXT:cell"},{"id":"T2680","span":{"begin":1005,"end":1015},"obj":"GO:0010467"},{"id":"T2681","span":{"begin":1053,"end":1060},"obj":"UBERON:0000922"},{"id":"T2682","span":{"begin":1064,"end":1069},"obj":"UBERON:0007023"},{"id":"T2683","span":{"begin":1070,"end":1076},"obj":"UBERON:0000062"},{"id":"T2684","span":{"begin":1192,"end":1200},"obj":"GO_EXT:biological_movement_or_translocation_process"},{"id":"T2685","span":{"begin":1307,"end":1315},"obj":"SO_EXT:sequence_variant_entity"},{"id":"T2686","span":{"begin":1436,"end":1442},"obj":"CHEBI_SO_EXT:molecular_label_or_mark_or_tag_process"},{"id":"T2687","span":{"begin":1443,"end":1453},"obj":"SO_EXT:transgenic_entity"},{"id":"T2688","span":{"begin":1635,"end":1641},"obj":"NCBITaxon:33208"},{"id":"T2689","span":{"begin":1807,"end":1818},"obj":"SO_EXT:transgenic_entity"},{"id":"T2690","span":{"begin":1822,"end":1828},"obj":"UBERON:0000479"},{"id":"T2691","span":{"begin":1901,"end":1907},"obj":"CHEBI_SO_EXT:molecular_label_or_mark_or_tag_process"},{"id":"T2692","span":{"begin":1961,"end":1973},"obj":"SO_EXT:sequence_alteration_process"},{"id":"T2693","span":{"begin":1978,"end":1983},"obj":"NCBITaxon:10088"},{"id":"T2694","span":{"begin":1984,"end":1990},"obj":"SO_EXT:0001026"}],"text":"Conclusions\nFrom these observations we conclude that the blue-shifted ECFP, and the red-shifted EYFP variants of wtGFP are both amenable to use in mice. Also since we have established lines of viable and fertile mice having widespread FP expression we have demonstrated that ECFP and EYFP represent developmentally neutral reporters. Since we were unable to obtain ES cells, embryos or mice with widespread expression of a RFP (DsRed1) we conclude that this reporter is not developmentally neutral or that its expression cannot be sustained at levels high enough for detection, and as such is not as versatile as other gene-based fluorescent reporters.\nECFP and EYFP can be distinguished on the basis of their unique non-overlapping spectral profiles, and chimeras comprised of ECFP and EYFP tagged compartments demonstrate that the two reporters can be simultaneously non-invasively visualized within the same embryo or adult organ. Therefore it should be possible to use flow cytometry to isolate cells expressing either or both of the reporters from embryos or adult organs [14].\nThese two reporters can also be used to create pairs of donors and acceptors for in vivo fluorescence energy transfer (FRET) [15]. Since the emission profiles of ECFP and EYFP are the least overlapping of all the usable GFP variants, these ECFP and EYFP currently represent the best combination for co-visualization and for use in multi-spectral double-tagged transgenic, chimeric and/or in vivo FRET experiments (reviewed in [16]).\nThese experiments have demonstrated the feasibility of monitoring multiple FP reporters non-invasively within a single animal, and have shown the developmental neutrality of the FP reporters employed. This should pave the way for novel strategies designed to incorporate the use of compound transgenics or tissue recombination or chimeric analyses where several compartments are to be tagged. This technology should provide new possibilities in manipulating the mouse genome, and non-invasively studying the consequences."}

{"project":"craft-ca-core-dev","denotations":[{"id":"T2644","span":{"begin":147,"end":151},"obj":"NCBITaxon:10088"},{"id":"T2645","span":{"begin":212,"end":216},"obj":"NCBITaxon:10088"},{"id":"T2646","span":{"begin":238,"end":248},"obj":"GO:0010467"},{"id":"T2647","span":{"begin":365,"end":373},"obj":"CL:0002322"},{"id":"T2648","span":{"begin":375,"end":382},"obj":"UBERON:0000922"},{"id":"T2649","span":{"begin":386,"end":390},"obj":"NCBITaxon:10088"},{"id":"T2650","span":{"begin":407,"end":417},"obj":"GO:0010467"},{"id":"T2651","span":{"begin":510,"end":520},"obj":"GO:0010467"},{"id":"T2652","span":{"begin":619,"end":623},"obj":"SO:0000704"},{"id":"T2653","span":{"begin":911,"end":917},"obj":"UBERON:0000922"},{"id":"T2654","span":{"begin":921,"end":926},"obj":"UBERON:0007023"},{"id":"T2655","span":{"begin":927,"end":932},"obj":"UBERON:0000062"},{"id":"T2656","span":{"begin":1005,"end":1015},"obj":"GO:0010467"},{"id":"T2657","span":{"begin":1053,"end":1060},"obj":"UBERON:0000922"},{"id":"T2658","span":{"begin":1064,"end":1069},"obj":"UBERON:0007023"},{"id":"T2659","span":{"begin":1070,"end":1076},"obj":"UBERON:0000062"},{"id":"T2660","span":{"begin":1635,"end":1641},"obj":"NCBITaxon:33208"},{"id":"T2661","span":{"begin":1822,"end":1828},"obj":"UBERON:0000479"},{"id":"T2662","span":{"begin":1978,"end":1983},"obj":"NCBITaxon:10088"},{"id":"T2663","span":{"begin":1984,"end":1990},"obj":"SO:0001026"}],"text":"Conclusions\nFrom these observations we conclude that the blue-shifted ECFP, and the red-shifted EYFP variants of wtGFP are both amenable to use in mice. Also since we have established lines of viable and fertile mice having widespread FP expression we have demonstrated that ECFP and EYFP represent developmentally neutral reporters. Since we were unable to obtain ES cells, embryos or mice with widespread expression of a RFP (DsRed1) we conclude that this reporter is not developmentally neutral or that its expression cannot be sustained at levels high enough for detection, and as such is not as versatile as other gene-based fluorescent reporters.\nECFP and EYFP can be distinguished on the basis of their unique non-overlapping spectral profiles, and chimeras comprised of ECFP and EYFP tagged compartments demonstrate that the two reporters can be simultaneously non-invasively visualized within the same embryo or adult organ. Therefore it should be possible to use flow cytometry to isolate cells expressing either or both of the reporters from embryos or adult organs [14].\nThese two reporters can also be used to create pairs of donors and acceptors for in vivo fluorescence energy transfer (FRET) [15]. Since the emission profiles of ECFP and EYFP are the least overlapping of all the usable GFP variants, these ECFP and EYFP currently represent the best combination for co-visualization and for use in multi-spectral double-tagged transgenic, chimeric and/or in vivo FRET experiments (reviewed in [16]).\nThese experiments have demonstrated the feasibility of monitoring multiple FP reporters non-invasively within a single animal, and have shown the developmental neutrality of the FP reporters employed. This should pave the way for novel strategies designed to incorporate the use of compound transgenics or tissue recombination or chimeric analyses where several compartments are to be tagged. This technology should provide new possibilities in manipulating the mouse genome, and non-invasively studying the consequences."}

{"project":"2_test","denotations":[{"id":"12079497-10951501-8577609","span":{"begin":1078,"end":1080},"obj":"10951501"},{"id":"12079497-10087619-8577610","span":{"begin":1209,"end":1211},"obj":"10087619"},{"id":"12079497-11219608-8577611","span":{"begin":1510,"end":1512},"obj":"11219608"}],"text":"Conclusions\nFrom these observations we conclude that the blue-shifted ECFP, and the red-shifted EYFP variants of wtGFP are both amenable to use in mice. Also since we have established lines of viable and fertile mice having widespread FP expression we have demonstrated that ECFP and EYFP represent developmentally neutral reporters. Since we were unable to obtain ES cells, embryos or mice with widespread expression of a RFP (DsRed1) we conclude that this reporter is not developmentally neutral or that its expression cannot be sustained at levels high enough for detection, and as such is not as versatile as other gene-based fluorescent reporters.\nECFP and EYFP can be distinguished on the basis of their unique non-overlapping spectral profiles, and chimeras comprised of ECFP and EYFP tagged compartments demonstrate that the two reporters can be simultaneously non-invasively visualized within the same embryo or adult organ. Therefore it should be possible to use flow cytometry to isolate cells expressing either or both of the reporters from embryos or adult organs [14].\nThese two reporters can also be used to create pairs of donors and acceptors for in vivo fluorescence energy transfer (FRET) [15]. Since the emission profiles of ECFP and EYFP are the least overlapping of all the usable GFP variants, these ECFP and EYFP currently represent the best combination for co-visualization and for use in multi-spectral double-tagged transgenic, chimeric and/or in vivo FRET experiments (reviewed in [16]).\nThese experiments have demonstrated the feasibility of monitoring multiple FP reporters non-invasively within a single animal, and have shown the developmental neutrality of the FP reporters employed. This should pave the way for novel strategies designed to incorporate the use of compound transgenics or tissue recombination or chimeric analyses where several compartments are to be tagged. This technology should provide new possibilities in manipulating the mouse genome, and non-invasively studying the consequences."}