Nascent Connections: R-Loops and Chromatin Patterning

被引:154
作者
Chedin, Frederic [1 ,2 ]
机构
[1] Univ Calif Davis, Dept Mol & Cellular Biol, One Shields Ave, Davis, CA 95616 USA
[2] Univ Calif Davis, Genome Ctr, One Shields Ave, Davis, CA 95616 USA
关键词
RNA-POLYMERASE-II; CLASS SWITCH RECOMBINATION; CPG ISLAND PROMOTERS; DNA-DAMAGE RESPONSE; LONG NONCODING RNAS; FORMATION IN-VITRO; GENOME INSTABILITY; HISTONE H3; TRANSCRIPTION ELONGATION; GC SKEW;
D O I
10.1016/j.tig.2016.10.002
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
RNA molecules, such as long noncoding RNAs (IncRNAs), have critical roles in regulating gene expression, chromosome architecture, and the modification states of chromatin. Recent developments suggest that RNA also influences gene expression and chromatin patterns through the interaction of nascent transcripts with their DNA template via the formation of co-transcriptional R-loop structures. R-loop formation over specific, conserved, hotspots occurs at thousands of genes in mammalian genomes and represents an important and dynamic feature of mammalian chromatin. Here, focusing primarily on mammalian systems, I describe the accumulating connections and possible mechanisms linking R-loop formation and chromatin patterning. The possible contribution of aberrant R-loops to pathological conditions is also discussed.
引用
收藏
页码:828 / 838
页数:11
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