| Literature DB >> 27027998 |
Gueorgui Kratassiouk1,2,3, Linda L Pritchard1,2,3, Sylvain Cuvellier1,2,3,4, Andrii Vislovukh1,2,3,5, Qingwei Meng1,2,3,6, Regina Groisman1,2,3, Cindy Degerny1,2,3, Evgeny Deforzh1,2,3, Annick Harel-Bellan1,2,3, Irina Groisman1,2,3.
Abstract
MicroRNAs (miRNAs) in the AGO-containing RISC complex control messenger RNA (mRNA) translation by binding to mRNA 3' untranslated region (3'UTR). The relationship between miRNAs and other regulatory factors that also bind to mRNA 3'UTR, such as CPEB1 (cytoplasmic polyadenylation element-binding protein), remains elusive. We found that both CPEB1 and miR-15b control the expression of WEE1, a key mammalian cell cycle regulator. Together, they repress WEE1 protein expression during G1 and S-phase. Interestingly, the 2 factors lose their inhibitory activity at the G2/M transition, at the time of the cell cycle when WEE1 expression is maximal, and, moreover, rather activate WEE1 translation in a synergistic manner. Our data show that translational regulation by RISC and CPEB1 is essential in cell cycle control and, most importantly, is coordinated, and can be switched from inhibition to activation during the cell cycle.Entities:
Keywords: CPEB1; WEE1; cell cycle; cytoplasmic polyadenylation; miR-15b; translational regulation
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Year: 2016 PMID: 27027998 PMCID: PMC4845936 DOI: 10.1080/15384101.2016.1147631
Source DB: PubMed Journal: Cell Cycle ISSN: 1551-4005 Impact factor: 4.534