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驱动蛋白 5B(KIF5B)对于雌性减数分裂的进展和有丝分裂细胞中染色体的正确分离是必需的。

Kinesin 5B (KIF5B) is required for progression through female meiosis and proper chromosomal segregation in mitotic cells.

机构信息

Departments of Therapeutic Radiology and Genetics and The Yale Comprehensive Cancer Center, New Haven, CT, USA.

出版信息

PLoS One. 2013;8(4):e58585. doi: 10.1371/journal.pone.0058585. Epub 2013 Apr 1.

Abstract

The fidelity of chromosomal segregation during cell division is important to maintain chromosomal stability in order to prevent cancer and birth defects. Although several spindle-associated molecular motors have been shown to be essential for cell division, only a few chromosome arm-associated motors have been described. Here, we investigated the role of Kinesin 5b (Kif5b) during female mouse meiotic cell development and mitotic cell division. RNA interference (RNAi)-mediated silencing of Kif5b in mouse oocytes induced significant delay in germinal vesicle breakdown (GVBD) and failure in extrusion of the first polar body (PBE). In mitotic cells, knockdown of Kif5b leads to centrosome amplification and a chromosomal segregation defect. These data suggest that KIF5B is critical in suppressing chromosomal instability at the early stages of female meiotic cell development and mitotic cell division.

摘要

在细胞分裂过程中,染色体分离的保真度对于维持染色体稳定性以预防癌症和出生缺陷至关重要。尽管已经证明有几种纺锤体相关的分子马达对于细胞分裂是必不可少的,但仅有少数染色体臂相关的马达被描述。在这里,我们研究了 Kinesin 5b(Kif5b)在雌性小鼠减数分裂细胞发育和有丝分裂细胞分裂过程中的作用。RNA 干扰(RNAi)介导的 Kif5b 在小鼠卵母细胞中的沉默导致生发泡破裂(GVBD)显著延迟和第一次极体(PBE)挤出失败。在有丝分裂细胞中,Kif5b 的敲低导致中心体扩增和染色体分离缺陷。这些数据表明,KIF5B 在抑制雌性减数分裂细胞发育和有丝分裂细胞分裂早期的染色体不稳定性方面至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/baeb/3613343/5c4045ade680/pone.0058585.g001.jpg

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