A large-scale binding and functional map of human RNA-binding proteins

Author:

Van Nostrand Eric L.ORCID,Freese Peter,Pratt Gabriel A.,Wang Xiaofeng,Wei Xintao,Xiao Rui,Blue Steven M.,Chen Jia-YuORCID,Cody Neal A. L.,Dominguez Daniel,Olson Sara,Sundararaman BalajiORCID,Zhan Lijun,Bazile Cassandra,Bouvrette Louis Philip Benoit,Bergalet Julie,Duff Michael O.,Garcia Keri E.,Gelboin-Burkhart Chelsea,Hochman Myles,Lambert Nicole J.,Li Hairi,McGurk Michael P.,Nguyen Thai B.,Palden Tsultrim,Rabano InesORCID,Sathe Shashank,Stanton Rebecca,Su Amanda,Wang Ruth,Yee Brian A.,Zhou BingORCID,Louie Ashley L.,Aigner StefanORCID,Fu Xiang-DongORCID,Lécuyer Eric,Burge Christopher B.ORCID,Graveley Brenton R.,Yeo Gene W.

Abstract

AbstractMany proteins regulate the expression of genes by binding to specific regions encoded in the genome1. Here we introduce a new data set of RNA elements in the human genome that are recognized by RNA-binding proteins (RBPs), generated as part of the Encyclopedia of DNA Elements (ENCODE) project phase III. This class of regulatory elements functions only when transcribed into RNA, as they serve as the binding sites for RBPs that control post-transcriptional processes such as splicing, cleavage and polyadenylation, and the editing, localization, stability and translation of mRNAs. We describe the mapping and characterization of RNA elements recognized by a large collection of human RBPs in K562 and HepG2 cells. Integrative analyses using five assays identify RBP binding sites on RNA and chromatin in vivo, the in vitro binding preferences of RBPs, the function of RBP binding sites and the subcellular localization of RBPs, producing 1,223 replicated data sets for 356 RBPs. We describe the spectrum of RBP binding throughout the transcriptome and the connections between these interactions and various aspects of RNA biology, including RNA stability, splicing regulation and RNA localization. These data expand the catalogue of functional elements encoded in the human genome by the addition of a large set of elements that function at the RNA level by interacting with RBPs.

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3