Widespread RNA binding by chromatin-associated proteins

被引:177
作者
Hendrickson, David G. [1 ,2 ]
Kelley, David R. [1 ,2 ]
Tenen, Danielle [1 ,2 ]
Bernstein, Bradley [2 ]
Rinn, John L. [1 ,2 ,3 ]
机构
[1] Harvard Univ, Dept Stem Cell & Regenerat Biol, Cambridge, MA 02138 USA
[2] Broad Inst Harvard & MIT, Cambridge, MA 02142 USA
[3] Beth Israel Deaconess Med Ctr, Boston, MA 02215 USA
关键词
RNA; lncRNA; RNA-protein interaction; RIP-seq; Chromatin; LONG NONCODING RNA; MESSENGER-RNAS; X-CHROMOSOME; REGULATORY INTERACTIONS; WIDE IDENTIFICATION; GENE; GENOME; SITES; DNA; TRANSCRIPTION;
D O I
10.1186/s13059-016-0878-3
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background: Recent evidence suggests that RNA interaction can regulate the activity and localization of chromatin-associated proteins. However, it is unknown if these observations are specialized instances for a few key RNAs and chromatin factors in specific contexts, or a general mechanism underlying the establishment of chromatin state and regulation of gene expression. Results: Here, we perform formaldehyde RNA immunoprecipitation (fRIP-Seq) to survey the RNA associated with a panel of 24 chromatin regulators and traditional RNA binding proteins. For each protein that reproducibly bound measurable quantities of bulk RNA (90 % of the panel), we detect enrichment for hundreds to thousands of both noncoding and mRNA transcripts. Conclusion: For each protein, we find that the enriched sets of RNAs share distinct biochemical, functional, and chromatin properties. Thus, these data provide evidence for widespread specific and relevant RNA association across diverse classes of chromatin-modifying complexes.
引用
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页数:18
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