Publication:

Widespread RNA binding by chromatin-associated proteins

Loading...
Thumbnail Image

Open/View Files

Date

2016

Journal Title

Journal ISSN

Volume Title

Publisher

BioMed Central
The Harvard community has made this article openly available. Please share how this access benefits you.

Research Projects

Organizational Units

Journal Issue

Citation

G Hendrickson, David, David R. Kelley, Danielle Tenen, Bradley Bernstein, and John L. Rinn. 2016. “Widespread RNA binding by chromatin-associated proteins.” Genome Biology 17 (1): 28. doi:10.1186/s13059-016-0878-3. http://dx.doi.org/10.1186/s13059-016-0878-3.

Abstract

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. Electronic supplementary material The online version of this article (doi:10.1186/s13059-016-0878-3) contains supplementary material, which is available to authorized users.

Description

Research Data

Keywords

RNA, lncRNA, RNA-protein interaction, RIP-seq, Chromatin

Terms of Use

This article is made available under the terms and conditions applicable to Other Posted Material (LAA), as set forth at Terms of Service

Endorsement

Review

Supplemented By

Related Stories