DNA结合位点
DNA
生物
计算生物学
DNA结合蛋白
遗传学
DNA测序
基因
转录因子
基因组
结合位点
抄写(语言学)
序列母题
发起人
基因表达
哲学
语言学
作者
Gwenaël Badis,Michael F. Berger,Anthony Philippakis,Shaheynoor Talukder,Andrew R. Gehrke,Savina Jaeger,Esther T. Chan,Genita Metzler,Anastasia Vedenko,Xiaoyu Chen,Hanna S. Kuznetsov,Chi-Fong Wang,David Coburn,Daniel E. Newburger,Quaid Morris,Timothy R. Hughes,Martha L. Bulyk
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2009-05-15
卷期号:324 (5935): 1720-1723
被引量:988
标识
DOI:10.1126/science.1162327
摘要
Transcriptional Regulation Gets More Complicated Sequence preferences of DNA binding proteins are a primary mechanism by which cells interpret the genome. A central goal in genome biology is to identify regulatory sequences in the genome; however, few proteins' DNA binding specificities have been characterized comprehensively. Badis et al. (p. 1720 , published online 14 May) studied 104 known and predicted transcription factors (TFs), spanning 22 structural classes, in the mouse genome. While traditional models of TF binding sites are based on a single collection of highly similar DNA sequences, binding profiles were represented better by multiple motifs. Roughly half of the TFs recognized distinct primary and secondary motifs that are different from each other. At least some of these interaction modes appeared to be attributable to biophysically distinct protein conformations, adding to the complexity of transcriptional regulation.
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