ATP-dependent chromatin remodeling shapes the long noncoding RNA landscape

被引:40
作者
Alcid, Eric A. [1 ,2 ]
Tsukiyama, Toshio [1 ]
机构
[1] Fred Hutchinson Canc Res Ctr, Div Basic Sci, Seattle, WA 98109 USA
[2] Univ Washington, Fred Hutchinson Canc Res Ctr, Mol & Cellular Biol Program, Seattle, WA 98195 USA
关键词
chromatin; chromatin remodeling; lncRNAs; antisense RNAs; BIDIRECTIONAL PROMOTERS; HISTONE MODIFICATION; CELL-FATE; TRANSCRIPTION; INITIATION; REGIONS; DEACETYLATION; ORGANIZATION; TERMINATION; EXPRESSION;
D O I
10.1101/gad.250902.114
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Long noncoding RNAs (lncRNAs) are pervasively transcribed across eukaryotic genomes, but functions of only a very small subset of them have been demonstrated. This has led to active debate about whether many of them have any biological functions. In addition, very few regulators of lncRNAs have been identified. We developed a novel genetic screen using reconstituted RNAi in Saccharomyces cerevisiae and systematically identified a large number of putative lncRNA repressors. Among them, we found that four highly conserved chromatin remodeling factors are global lncRNA repressors that play major roles in shaping the eukaryotic lncRNA transcriptome. Importantly, we identified >250 antisense lncRNAs (CRRATs [chromatin remodeling-repressed antisense transcripts]) whose repression by these chromatin remodeling factors is required for the maintenance of normal levels of overlapping mRNA transcripts. Our results strongly suggest that regulation of mRNA through repression of antisense lncRNAs is far more broadly used than previously appreciated.
引用
收藏
页码:2348 / 2360
页数:13
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