| Literature DB >> 28157508 |
Hong Han1, Ulrich Braunschweig2, Thomas Gonatopoulos-Pournatzis2, Robert J Weatheritt3, Calley L Hirsch4, Kevin C H Ha1, Ernest Radovani1, Syed Nabeel-Shah1, Tim Sterne-Weiler2, Juli Wang2, Dave O'Hanlon2, Qun Pan2, Debashish Ray2, Hong Zheng2, Frederick Vizeacoumar4, Alessandro Datti4, Lilia Magomedova5, Carolyn L Cummins5, Timothy R Hughes1, Jack F Greenblatt1, Jeffrey L Wrana6, Jason Moffat1, Benjamin J Blencowe7.
Abstract
Networks of coordinated alternative splicing (AS) events play critical roles in development and disease. However, a comprehensive knowledge of the factors that regulate these networks is lacking. We describe a high-throughput system for systematically linking trans-acting factors to endogenous RNA regulatory events. Using this system, we identify hundreds of factors associated with diverse regulatory layers that positively or negatively control AS events linked to cell fate. Remarkably, more than one-third of the regulators are transcription factors. Further analyses of the zinc finger protein Zfp871 and BTB/POZ domain transcription factor Nacc1, which regulate neural and stem cell AS programs, respectively, reveal roles in controlling the expression of specific splicing regulators. Surprisingly, these proteins also appear to regulate target AS programs via binding RNA. Our results thus uncover a large "missing cache" of splicing regulators among annotated transcription factors, some of which dually regulate AS through direct and indirect mechanisms.Entities:
Keywords: RNA interference; SPAR-seq; alternative splicing; chromatin; embryonic stem cells; high-throughput screening; neuroblastoma cells; spliceosome; splicing factors; transcription factors
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Year: 2017 PMID: 28157508 DOI: 10.1016/j.molcel.2017.01.011
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 17.970