Circadian Enhancers Coordinate Multiple Phases of Rhythmic Gene Transcription In Vivo

被引:179
作者
Fang, Bin [1 ,2 ]
Everett, Logan J. [1 ,2 ]
Jager, Jennifer [1 ,2 ]
Briggs, Erika [1 ,2 ]
Armour, Sean M. [1 ,2 ]
Feng, Dan [1 ,2 ]
Roy, Ankur [1 ,2 ]
Gerhart-Hines, Zachary [1 ,2 ]
Sun, Zheng [1 ,2 ]
Lazar, Mitchell A. [1 ,2 ]
机构
[1] Univ Penn, Div Endocrinol Diabet & Metab, Dept Med, Dept Genet, Philadelphia, PA 19104 USA
[2] Univ Penn, Perelman Sch Med, Inst Diabet Obes & Metab, Philadelphia, PA 19104 USA
关键词
REV-ERB-ALPHA; NUCLEAR RECEPTORS; CLOCK; BINDING; EXPRESSION; MOUSE; LIVER; DBP; METABOLISM; ACTIVATION;
D O I
10.1016/j.cell.2014.10.022
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Mammalian transcriptomes display complex circadian rhythms with multiple phases of gene expression that cannot be accounted for by current models of the molecular clock. We have determined the underlying mechanisms by measuring nascent RNA transcription around the clock in mouse liver. Unbiased examination of enhancer RNAs (eRNAs) that cluster in specific circadian phases identified functional enhancers driven by distinct transcription factors (TFs). We further identify on a global scale the components of the TF cistromes that function to orchestrate circadian gene expression. Integrated genomic analyses also revealed mechanisms by which a single circadian factor controls opposing transcriptional phases. These findings shed light on the diversity and specificity of TF function in the generation of multiple phases of circadian gene transcription in a mammalian organ.
引用
收藏
页码:1140 / 1152
页数:13
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