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Systematic discovery of regulatory motifs in human promoters and 3′ UTRs by comparison of several mammals
被引:1464
作者:

Xie, XH
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机构: MIT, Broad Inst, Cambridge, MA 02141 USA

Lu, J
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机构: MIT, Broad Inst, Cambridge, MA 02141 USA

Kulbokas, EJ
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机构: MIT, Broad Inst, Cambridge, MA 02141 USA

Golub, TR
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机构: MIT, Broad Inst, Cambridge, MA 02141 USA

Mootha, V
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机构: MIT, Broad Inst, Cambridge, MA 02141 USA

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Lander, ES
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MIT, Broad Inst, Cambridge, MA 02141 USA MIT, Broad Inst, Cambridge, MA 02141 USA

Kellis, M
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机构: MIT, Broad Inst, Cambridge, MA 02141 USA
机构:
[1] MIT, Broad Inst, Cambridge, MA 02141 USA
[2] Harvard, Broad Inst, Cambridge, MA 02141 USA
[3] MIT, Whitehead Inst Biomed Res, Cambridge, MA 02139 USA
[4] MIT, Comp Sci & Artificial Intelligence Lab, Cambridge, MA 02139 USA
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D O I:
10.1038/nature03441
中图分类号:
O [数理科学和化学];
P [天文学、地球科学];
Q [生物科学];
N [自然科学总论];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
Comprehensive identification of all functional elements encoded in the human genome is a fundamental need in biomedical research. Here, we present a comparative analysis of the human, mouse, rat and dog genomes to create a systematic catalogue of common regulatory motifs in promoters and 30 untranslated regions ( 3 0 UTRs). The promoter analysis yields 174 candidate motifs, including most previously known transcription-factor binding sites and 105 new motifs. The 3'-UTR analysis yields 106 motifs likely to be involved in post-transcriptional regulation. Nearly one-half are associated with microRNAs ( miRNAs), leading to the discovery of many new miRNA genes and their likely target genes. Our results suggest that previous estimates of the number of human miRNA genes were low, and that miRNAs regulate at least 20% of human genes. The overall results provide a systematic view of gene regulation in the human, which will be refined as additional mammalian genomes become available.
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页码:338 / 345
页数:8
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