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PICK1基因缺陷通过破坏顶体形成导致小鼠雄性不育。

PICK1 deficiency causes male infertility in mice by disrupting acrosome formation.

作者信息

Xiao Nan, Kam Chuen, Shen Chong, Jin Wenying, Wang Junqi, Lee Kwong Man, Jiang Liwen, Xia Jun

机构信息

Department of Biochemistry, The Hong Kong University of Science and Technology, Clear Water Bay, Kowloon, Hong Kong, People's Republic of China.

出版信息

J Clin Invest. 2009 Apr;119(4):802-12. doi: 10.1172/JCI36230. Epub 2009 Mar 2.

Abstract

Protein interacting with C kinase 1 (PICK1) is a peripheral membrane protein involved in protein trafficking, a function that has been well characterized in neurons. Here, we report that male mice deficient in PICK1 are infertile and have a phenotype resembling the human disease globozoospermia. The primary defect in the testes of Pick1-knockout mice was fragmentation of acrosomes in the early stages of spermiogenesis. This fragmentation was followed by defects in nuclear elongation and mitochondrial sheath formation, leading to round-headed sperm, reduced sperm count, and severely impaired sperm motility. We found that PICK1 interacted with Golgi-associated PDZ- and coiled-coil motif-containing protein (GOPC) and the primary catalytic subunit of protein kinase 2 (CK2alpha'), proteins whose deficiencies lead to globozoospermia in mice. PICK1 was highly expressed in round spermatids and localized to Golgi-derived proacrosomal granules. GOPC colocalized with PICK1 in the Golgi region and facilitated formation of PICK1-positive clusters. Furthermore, there was an increase in apoptosis in the seminiferous tubules of Pick1-/- mice, a phenotype also seen in CK2alpha'-deficient mice. Our results suggest that PICK1 is involved in vesicle trafficking from the Golgi apparatus to the acrosome and cooperates with other proteins such as GOPC and CK2alpha' in acrosome biogenesis.

摘要

与C激酶1相互作用的蛋白(PICK1)是一种外周膜蛋白,参与蛋白质转运,该功能在神经元中已得到充分表征。在此,我们报告PICK1基因缺失的雄性小鼠不育,且具有类似于人类疾病圆头精子症的表型。Pick1基因敲除小鼠睾丸的主要缺陷是精子发生早期顶体碎片化。这种碎片化之后是核伸长和线粒体鞘形成缺陷,导致圆头精子、精子数量减少以及精子活力严重受损。我们发现PICK1与高尔基体相关的含PDZ和卷曲螺旋基序的蛋白(GOPC)以及蛋白激酶2的主要催化亚基(CK2α')相互作用,这些蛋白的缺陷会导致小鼠出现圆头精子症。PICK1在圆形精子细胞中高度表达,并定位于高尔基体衍生的前顶体颗粒。GOPC与PICK1在高尔基体区域共定位,并促进PICK1阳性簇的形成。此外,Pick1-/-小鼠的生精小管中细胞凋亡增加,这一表型在CK2α'缺陷小鼠中也可见。我们的结果表明,PICK1参与从高尔基体到顶体的囊泡运输,并在顶体生物发生过程中与GOPC和CK2α'等其他蛋白协同作用。

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