The Sperm Laboratory, College of Life Sciences, Zhejiang University, Hangzhou, China.
Inspection and Quarantine Technique Centre of Fujian Entry-Exit Inspection and Quarantine Bureau, Fujian Provincial Key Laboratory of Inspection and Quarantine Technology Research, Fuzhou, China.
Biol Reprod. 2017 Feb 1;96(2):267-276. doi: 10.1095/biolreprod.116.144113.
Kinesins are essential for the proper function of many types of polar cells, including epithelial cells, neurons, and sperm. Spermatogenesis is closely associated with many different kinesins. These kinesins participate in several fundamental processes, including mitotic and meiotic division, essential organelle transport, and the biogenesis of peculiar structures for the formation of mature sperm. Kinesin-13, kinesin-8, and the chromokinesin families cooperate to ensure normal sister chromatid congression and segregation. The kinesin-8 family motor KIF18A, kinesin-12 motors PAKRP/kinesin12A and PAKRP1L/kinesin12B, and other kinesin-like motors are essential in the process of homologous chromosome pairing and in the separation to create haploid gametes. During spermiogenesis, the responsibility of a handful of kinesin members lies in the maturation of spermatids into mature, motile, and intact spermatozoa. Such roles are completed upon the release of viable and functional sperm into the lumen of seminiferous tubules. In this process, KIFC1, KIF5C, KRP3A, and KRP3B may be involved in acrosome biogenesis; KIFC1, KIFC5, CHO2, KIF17b, and KIF3A probably contribute to nuclear shaping; KIF17b, KIF3A, and KLC3 are implicated in the tail formation process; and KIF20 and KRP3 likely participate in sperm translocation. KIF17b also exhibited postmeiosis transcriptional activities that are critical for the dramatic alterations observed in nuclear and cytoplasmic structures. This review summarizes the roles of kinesins during mitosis, meiosis, and spermiogenesis, and proposes several important issues for further investigation.
驱动蛋白是许多极性细胞类型(包括上皮细胞、神经元和精子)正常功能所必需的。精子发生与许多不同的驱动蛋白密切相关。这些驱动蛋白参与了几个基本过程,包括有丝分裂和减数分裂、必需的细胞器运输以及形成成熟精子的特殊结构的生物发生。驱动蛋白-13、驱动蛋白-8 和染色体驱动蛋白家族合作以确保姐妹染色单体正确聚集和分离。驱动蛋白-8 家族的马达蛋白 KIF18A、驱动蛋白-12 马达 PAKRP/kinesin12A 和 PAKRP1L/kinesin12B 以及其他类驱动蛋白马达对于同源染色体配对和分离以产生单倍体配子的过程是必不可少的。在精子发生过程中,少数驱动蛋白成员的责任在于将精原细胞成熟为具有活力和运动能力的完整精子。当有活力和功能的精子释放到曲细精管腔中时,这些作用就完成了。在这个过程中,KIFC1、KIF5C、KRP3A 和 KRP3B 可能参与顶体生物发生;KIFC1、KIFC5、CHO2、KIF17b 和 KIF3A 可能有助于核形成;KIF17b、KIF3A 和 KLC3 可能参与尾巴形成过程;KIF20 和 KRP3 可能参与精子转运。KIF17b 还表现出减数分裂后的转录活性,这对于观察到的核和细胞质结构的剧烈变化至关重要。本综述总结了驱动蛋白在有丝分裂、减数分裂和精子发生过程中的作用,并提出了几个需要进一步研究的重要问题。