| Literature DB >> 27050523 |
Benjamin Cieply1, Juw Won Park2, Angela Nakauka-Ddamba3, Thomas W Bebee1, Yang Guo4, Xuequn Shang5, Christopher J Lengner3, Yi Xing6, Russ P Carstens7.
Abstract
Alternative splicing (AS) plays a critical role in cell fate transitions, development, and disease. Recent studies have shown that AS also influences pluripotency and somatic cell reprogramming. We profiled transcriptome-wide AS changes that occur during reprogramming of fibroblasts to pluripotency. This analysis revealed distinct phases of AS, including a splicing program that is unique to transgene-independent induced pluripotent stem cells (iPSCs). Changes in the expression of AS factors Zcchc24, Esrp1, Mbnl1/2, and Rbm47 were demonstrated to contribute to phase-specific AS. RNA-binding motif enrichment analysis near alternatively spliced exons provided further insight into the combinatorial regulation of AS during reprogramming by different RNA-binding proteins. Ectopic expression of Esrp1 enhanced reprogramming, in part by modulating the AS of the epithelial specific transcription factor Grhl1. These data represent a comprehensive temporal analysis of the dynamic regulation of AS during the acquisition of pluripotency.Entities:
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Year: 2016 PMID: 27050523 PMCID: PMC5718363 DOI: 10.1016/j.celrep.2016.03.025
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423