| Literature DB >> 27068461 |
Anne E Conway1, Eric L Van Nostrand2, Gabriel A Pratt3, Stefan Aigner2, Melissa L Wilbert2, Balaji Sundararaman2, Peter Freese4, Nicole J Lambert4, Shashank Sathe2, Tiffany Y Liang2, Anthony Essex5, Severine Landais5, Christopher B Burge4, D Leanne Jones6, Gene W Yeo7.
Abstract
Human pluripotent stem cells (hPSCs) require precise control of post-transcriptional RNA networks to maintain proliferation and survival. Using enhanced UV crosslinking and immunoprecipitation (eCLIP), we identify RNA targets of the IMP/IGF2BP family of RNA-binding proteins in hPSCs. At the broad region and binding site levels, IMP1 and IMP2 show reproducible binding to a large and overlapping set of 3' UTR-enriched targets. RNA Bind-N-seq applied to recombinant full-length IMP1 and IMP2 reveals CA-rich motifs that are enriched in eCLIP-defined binding sites. We observe that IMP1 loss in hPSCs recapitulates IMP1 phenotypes, including a reduction in cell adhesion and increase in cell death. For cell adhesion, we find IMP1 maintains levels of integrin mRNA specifically regulating RNA stability of ITGB5 in hPSCs. Additionally, we show that IMP1 can be linked to hPSC survival via direct target BCL2. Thus, transcriptome-wide binding profiles identify hPSC targets modulating well-characterized IMP1 roles.Entities:
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Year: 2016 PMID： 27068461 PMCID： PMC4839292 DOI： 10.1016/j.celrep.2016.03.052
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423