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Loss of function of KIF1B impairs oocyte meiotic maturation and early embryonic development in mice

机译:KIF1B功能丧失会损害小鼠卵母细胞的减数分裂成熟和早期胚胎发育

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摘要

Kinesin family member 1B (KIF1B) is an important microtubule-dependent monomeric motor in mammals, although little is known about its role in meiosis. We profiled KIF1B expression and localization during oocyte maturation and early embryonic development in mice, revealing a dynamic pattern throughout meiotic progression. Depletion or inhibition of KIF1B leads to abnormal polar body extrusion, disordered spindle dynamics, defects in chromosome congression, increased aneuploidy, and impaired embryonic development. Further, KIF1B depletion affects the distribution of mitochondria and abundance of ATP. Taken together, our study demonstrates that mouse KIF1B is important for spindle assembly, chromosome congression, and mitochondrial distribution during oocyte maturation and early embryonic development. Mol. Reprod. Dev. 83: 1027-1040, 2016 (c) 2016 Wiley Periodicals, Inc.
机译:驱动蛋白家族成员1B(KIF1B)是哺乳动物中一种重要的依赖微管的单体运动,尽管对其减数分裂的作用知之甚少。我们在小鼠卵母细胞成熟和早期胚胎发育过程中分析了KIF1B的表达和定位,揭示了整个减数分裂进程的动态模式。 KIF1B的耗尽或抑制会导致极体挤压异常,纺锤体动力学紊乱,染色体聚合缺陷,非整倍性增加以及胚胎发育受损。此外,KIF1B耗竭会影响线粒体的分布和ATP的丰度。两者合计,我们的研究表明,小鼠KIF1B对于卵母细胞成熟和早期胚胎发育过程中的纺锤体组装,染色体大会和线粒体分布很重要。大声笑责备。开发人员83:1027-1040,2016(c)2016 Wiley Periodicals,Inc.

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