Repression of Divergent Noncoding Transcription by a Sequence-Specific Transcription Factor

被引:25
作者
Wu, Andrew C. K. [1 ]
Patel, Harshil [2 ]
Chia, Minghao [1 ]
Moretto, Fabien [1 ]
Frith, David [3 ]
Snijders, Ambrosius P. [3 ]
van Werven, Folkert J. [1 ]
机构
[1] Francis Crick Inst, Cell Fate & Gene Regulat Lab, 1 Midland Rd, London NW1 1AT, England
[2] Francis Crick Inst, Bioinformat & Biostat, 1 Midland Rd, London NW1 1AT, England
[3] Francis Crick Inst, Prot Anal & Prote Platform, 1 Midland Rd, London NW1 1AT, England
基金
英国医学研究理事会; 英国惠康基金;
关键词
GENOME-WIDE; PERVASIVE TRANSCRIPTION; BIDIRECTIONAL PROMOTERS; NUCLEOSOME POSITION; CHROMATIN-STRUCTURE; GENE DELETION; DEGRON SYSTEM; RNA; BINDING; IDENTIFICATION;
D O I
10.1016/j.molcel.2018.10.018
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
Many active eukaryotic gene promoters exhibit divergent noncoding transcription, but the mechanisms restricting expression of these transcripts are not well understood. Here, we demonstrate how a sequence-specific transcription factor represses divergent noncoding transcription at highly expressed genes in yeast. We find that depletion of the transcription factor Rap1 induces noncoding transcription in a large fraction of Rap1-regulated gene promoters. Specifically, Rap1 prevents transcription initiation at cryptic promoters near its binding sites, which is uncoupled from transcription regulation in the protein-coding direction. We further provide evidence that Rap1 acts independently of previously described chromatin-based mechanisms to repress cryptic or divergent transcription. Finally, we show that divergent transcription in the absence of Rap1 is elicited by the RSC chromatin remodeler. We propose that a sequence-specific transcription factor limits access of basal transcription machinery to regulatory elements and adjacent sequences that act as divergent cryptic promoters, thereby providing directionality toward productive transcription.
引用
收藏
页码:942 / +
页数:20
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