期刊
SCIENCE
卷 346, 期 6212, 页码 1007-1012出版社
AMER ASSOC ADVANCEMENT SCIENCE
DOI: 10.1126/science.1246426
关键词
-
资金
- NIH grants [U54HG007010, 1RC2HG005654, R37DK44746, 2R01HD04399709]
- NSF Graduate Research Fellowship [DGE-071824]
- MRC [MC_UU_12009/2] Funding Source: UKRI
- Medical Research Council [MC_UU_12009/2] Funding Source: researchfish
To study the evolutionary dynamics of regulatory DNA, we mapped >1.3 million deoxyribonuclease I-hypersensitive sites (DHSs) in 45 mouse cell and tissue types, and systematically compared these with human DHS maps from orthologous compartments. We found that the mouse and human genomes have undergone extensive cis-regulatory rewiring that combines branch-specific evolutionary innovation and loss with widespread repurposing of conserved DHSs to alternative cell fates, and that this process is mediated by turnover of transcription factor (TF) recognition elements. Despite pervasive evolutionary remodeling of the location and content of individual cis-regulatory regions, within orthologous mouse and human cell types the global fraction of regulatory DNA bases encoding recognition sites for each TF has been strictly conserved. Our findings provide new insights into the evolutionary forces shaping mammalian regulatory DNA landscapes.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据