| Literature DB >> 27472084 |
Jin-Mei Cheng1,2, Jian Li1,2, Ji-Xin Tang1,2, Su-Ren Chen1, Shou-Long Deng1, Cheng Jin1,2, Yan Zhang1, Xiu-Xia Wang1, Chen-Xi Zhou1, Yi-Xun Liu1.
Abstract
Increases in the aneuploidy rate caused by the deterioration of cohesion with increasing maternal age have been well documented. However, the molecular mechanism for the loss of cohesion in aged oocytes remains unknown. In this study, we found that intracellular pH (pHi) was elevated in aged oocytes, which might disturb the structure of the cohesin ring to induce aneuploidy. We observed for the first time that full-grown germinal vesicle (GV) oocytes displayed an increase in pHi with advancing age in CD1 mice. Furthermore, during the in vitro oocyte maturation process, the pHi was maintained at a high level, up to ∼7.6, in 12-month-old mice. Normal pHi is necessary to maintain protein localization and function. Thus, we put forward a hypothesis that the elevated oocyte pHi might be related to the loss of cohesion and the increased aneuploidy in aged mice. Through the in vitro alkalinization treatment of young oocytes, we observed that the increased pHi caused an increase in the aneuploidy rate and the sister inter-kinetochore (iKT) distance associated with the strength of cohesion and caused a decline in the cohesin subunit SMC3 protein level. Young oocytes with elevated pHi exhibited substantially the increase in chromosome misalignment.Entities:
Keywords: aging; alkalinization; chromosome aneuploidy; cohesion; oocytes; pHi
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Year: 2016 PMID: 27472084 PMCID: PMC5026820 DOI: 10.1080/15384101.2016.1201255
Source DB: PubMed Journal: Cell Cycle ISSN: 1551-4005 Impact factor: 4.534