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Enhancer RNAs: A missing regulatory layer in gene transcription

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【作者】 Renfang MaoYuanyuan WuYue MingYuanpei XuShouyan WangXia ChenXiaoying WangYihui Fan

【Author】 Renfang Mao;Yuanyuan Wu;Yue Ming;Yuanpei Xu;Shouyan Wang;Xia Chen;Xiaoying Wang;Yihui Fan;Department of Pathophysiology, School of Medicine, Nantong University;Basic Medical Research Center, School of Medicine, Nantong University;Department of Immunology, School of Medicine, Nantong University;

【通讯作者】 Yihui Fan;

【机构】 Department of Pathophysiology, School of Medicine, Nantong UniversityBasic Medical Research Center, School of Medicine, Nantong UniversityDepartment of Immunology, School of Medicine, Nantong University

【摘要】 Enhancers and super-enhancers exert indispensable roles in maintaining cell identity through spatiotemporally regulating gene transcription. Meanwhile, active enhancers and super-enhancers also produce transcripts termed enhancer RNAs(eRNAs) from their DNA elements. Although enhancers have been identified for more than 30 years, widespread transcription from enhancers are just discovered by genome-wide sequencing and considered as the key to understand longstanding questions in gene transcription. RNA-transcribed enhancers are marked by histone modifications such as H3K4m1/2 and H3K27Ac, and enriched with transcription regulatory factors such as LDTFs, P300, CBP, BRD4 and MED1. Those regulatory factors might constitute a Mega-Trans-like complex to potently activate enhancers. Compared to mRNAs, eRNAs are quite unstable and play roles at local.Functionally, it has been shown that e RNAs promote formation of enhancer-promoter loops. Several studies also demonstrated that eRNAs help the binding of RNA polymerase II(RNAPII) or transition of paused RNAPII by de-association of the negative elongation factor(NELF) complex. Nevertheless, these proposed mechanisms are not universally accepted and still under controversy. Here, we comprehensively summarize the reported findings and make perspectives for future exploration. We also believe that super-enhancer derived RNAs(seRNAs) might be informative to understand the nature of super-enhancers.

【Abstract】 Enhancers and super-enhancers exert indispensable roles in maintaining cell identity through spatiotemporally regulating gene transcription. Meanwhile, active enhancers and super-enhancers also produce transcripts termed enhancer RNAs(eRNAs) from their DNA elements. Although enhancers have been identified for more than 30 years, widespread transcription from enhancers are just discovered by genome-wide sequencing and considered as the key to understand longstanding questions in gene transcription. RNA-transcribed enhancers are marked by histone modifications such as H3K4m1/2 and H3K27Ac, and enriched with transcription regulatory factors such as LDTFs, P300, CBP, BRD4 and MED1. Those regulatory factors might constitute a Mega-Trans-like complex to potently activate enhancers. Compared to mRNAs, eRNAs are quite unstable and play roles at local.Functionally, it has been shown that e RNAs promote formation of enhancer-promoter loops. Several studies also demonstrated that eRNAs help the binding of RNA polymerase II(RNAPII) or transition of paused RNAPII by de-association of the negative elongation factor(NELF) complex. Nevertheless, these proposed mechanisms are not universally accepted and still under controversy. Here, we comprehensively summarize the reported findings and make perspectives for future exploration. We also believe that super-enhancer derived RNAs(seRNAs) might be informative to understand the nature of super-enhancers.

【基金】 supported by the Distinguished Professorship Program of Jiangsu Province to Y.F;the National Natural Science Foundation of China(31770935,81641164,81600386,81471539,30801350);the Natural Science Foundation of Nantong University(14Z022);Postgraduate Research&Practice Innovation Program of Jiangsu Province(KYCX17_1933);Undergraduate Training Program for Innovation(201710304030Z)
  • 【文献出处】 Science China(Life Sciences) ,中国科学:生命科学(英文版) , 编辑部邮箱 ,2019年07期
  • 【分类号】Q75
  • 【网络出版时间】2018-12-28 09:21
  • 【被引频次】3
  • 【下载频次】30
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