首页> 美国卫生研究院文献>Aging (Albany NY) >KIFC1 is essential for normal spermatogenesis and its depletion results in early germ cell apoptosis in the Kuruma shrimp Penaeus (Marsupenaeus) japonicus
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KIFC1 is essential for normal spermatogenesis and its depletion results in early germ cell apoptosis in the Kuruma shrimp Penaeus (Marsupenaeus) japonicus

机译:KIFC1对于正常的精子发生是必不可少的其消耗会导致库鲁玛虾对虾(Marsupenaeus)japonicus早期生殖细胞凋亡。

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摘要

In order to explore the dynamic mechanisms during spermatogenesis of the penaeid prawns, the full length of was cloned from testis cDNA of through RACE. Both semi-quantitative RT-PCR and Western blot results indicated that KIFC1 was extensive expressed in different tissue of . Compared with other tissue, the highest expression of KIFC1 occurred in the testis. According to the immunofluorescence results, the KIFC1 protein was detected at each stage of whole process of spermatogenesis. In the spermatogonial phase, KIFC1 mainly dispersed in cytoplasm and co-localized with microtubules, while abundant KIFC1 signal was detected in the nucleus of spermatocytes. At the early stage of spermatids, KIFC1 was transported from the nucleus into the cytoplasm, and it assisted microtubule assembly onto one side of the nucleus. Finally, in mature sperm, it was weakly expressed in the acrosome. This implies that KIFC1 may participate in the mitosis of spermatogonia, meiosis of spermatocyte, and acrosome formation during spermiogenesis; it may also play functions in acrosome maintaining in mature sperm. In addition, the results of KIFC1 knockdown by dsRNA injection reveal that decreased KIFC1 expression may induce aberrant microtubule assembly, and it leads to spermatogonia and spermatocyte apoptosis.
机译:为了探索对虾对虾精子形成过程中的动力学机制,通过RACE从睾丸cDNA中克隆了全长对虾。半定量RT-PCR和Western印迹结果均表明KIFC1广泛表达于不同组织中。与其他组织相比,KIFC1的最高表达发生在睾丸中。根据免疫荧光结果,在精子发生整个过程的每个阶段都检测到了KIFC1蛋白。在精原细胞期,KIFC1主要分散在细胞质中并与微管共定位,而在精母细胞核中检测到丰富的KIFC1信号。在精子的早期阶段,KIFC1从细胞核转运到细胞质,并协助微管组装到细胞核的一侧。最后,在成熟的精子中,它在顶体中微弱表达。这意味着KIFC1可能参与精子发生过程中的精原细胞有丝分裂,精细胞减数分裂和顶体形成。它也可能在成熟精子的顶体维护中发挥作用。此外,通过dsRNA注射敲低KIFC1的结果表明,降低的KIFC1表达可能诱导微管装配异常,并导致精原细胞增多和精细胞凋亡。

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