Gene Loops Enhance Transcriptional Directionality

被引:178
作者
Tan-Wong, Sue Mei [2 ]
Zaugg, Judith B. [3 ]
Camblong, Jurgi [2 ]
Xu, Zhenyu [1 ]
Zhang, David W. [4 ]
Mischo, Hannah E. [2 ]
Ansari, Aseem Z. [4 ]
Luscombe, Nicholas M. [3 ,5 ,6 ]
Steinmetz, Lars M. [1 ]
Proudfoot, Nick J. [2 ]
机构
[1] European Mol Biol Lab, Genome Biol Unit, D-69117 Heidelberg, Germany
[2] Univ Oxford, Sir William Dunn Sch Pathol, Oxford OX1 3RE, England
[3] European Bioinformat Inst, European Mol Biol Lab, Cambridge CB10 1SD, England
[4] Univ Wisconsin, Dept Biochem, Madison, WI 53706 USA
[5] UCL, Genet Inst, London WC1E 6BT, England
[6] Canc Res UK London Res Inst, London WC2A 3LY, England
基金
美国国家科学基金会; 英国惠康基金;
关键词
RNA-POLYMERASE-II; COMPLEX; METHYLATION; TERMINATION; PROMOTERS; SSU72; CEREVISIAE; INITIATION; UPSTREAM; RECRUITS;
D O I
10.1126/science.1224350
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
Eukaryotic genomes are extensively transcribed, forming both messenger RNAs (mRNAs) and noncoding RNAs (ncRNAs). ncRNAs made by RNA polymerase II often initiate from bidirectional promoters (nucleosome-depleted chromatin) that synthesize mRNA and ncRNA in opposite directions. We demonstrate that, by adopting a gene-loop conformation, actively transcribed mRNA encoding genes restrict divergent transcription of ncRNAs. Because gene-loop formation depends on a protein factor (Ssu72) that coassociates with both the promoter and the terminator, the inactivation of Ssu72 leads to increased synthesis of promoter-associated divergent ncRNAs, referred to as Ssu72-restricted transcripts (SRTs). Similarly, inactivation of individual gene loops by gene mutation enhances SRT synthesis. We demonstrate that gene-loop conformation enforces transcriptional directionality on otherwise bidirectional promoters.
引用
收藏
页码:671 / 675
页数:5
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