Literature DB >> 33604343

RBM14 Modulates Tubulin Acetylation and Regulates Spindle Morphology During Meiotic Maturation in Mouse Oocytes.

Hao Qin1,2,3,4, Yi Qu1,2,3,4, Yi-Feng Yuan1,2,3,4, Yang-Yang Li1,2,3,4, Jie Qiao1,2,3,4,5.   

Abstract

RBM14 is an RNA-binding protein that regulates spindle integrity in mitosis; however, its functions during meiosis are still unclear. In this study, we discovered that RBM14 expression was down-regulated in oocytes from old mice. The RBM14 distribution at different stages of meiosis was explored, while it presents overlapped localization patterns with α-tubulin in MI- and MII-stage oocytes. Treatment of MI-stage oocytes with spindle-perturbing agents revealed that RBM14 was co-localized with microtubules. RBM14 knockdown with RBM14-specific morpholino showed that RBM14-depleted oocytes underwent symmetric division compared to the controls. RBM14 knockdown also resulted in spindle defects and chromosome abnormalities during oocyte maturation, presumably due to α-tubulin hyperacetylation. Co-immunoprecipitation analysis demonstrated that RBM14 is interacted with endogenous α-tubulin in mammalian cells. These findings indicate that RBM14 is an essential modulator of oocyte meiotic maturation by regulating α-tubulin acetylation to affect spindle morphology and chromosome alignment. Consequently, RBM14 represents a potential biomarker of oocyte quality and a novel therapeutic target in women with oocyte maturation failure.
Copyright © 2021 Qin, Qu, Yuan, Li and Qiao.

Entities:  

Keywords:  RBM14; acetylation; meiosis; oocyte; spindle

Year:  2021        PMID: 33604343      PMCID: PMC7884444          DOI: 10.3389/fcell.2021.635728

Source DB:  PubMed          Journal:  Front Cell Dev Biol        ISSN: 2296-634X


  34 in total

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Authors:  Jing Li; Chenxin Wang; Guihai Feng; Linlin Zhang; Guilai Chen; Hao Sun; Jiaqiang Wang; Ying Zhang; Qi Zhou; Wei Li
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  1 in total

1.  In Vivo and In Vitro Matured Oocytes From Mice of Advanced Reproductive Age Exhibit Alternative Splicing Processes for Mitochondrial Oxidative Phosphorylation.

Authors:  Hao Qin; Yi Qu; Rong Li; Jie Qiao
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  1 in total

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