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与BLOS2相互作用的SLX2在小鼠卵母细胞减数分裂成熟过程中差异表达。

SLX2 interacting with BLOS2 is differentially expressed during mouse oocyte meiotic maturation.

作者信息

Zhuang Xin-Jie, Shi Yu-Qiang, Xu Bo, Chen Lei, Tang Wen-Hao, Huang Jin, Lian Ying, Liu Ping, Qiao Jie

机构信息

Center for Reproductive Medicine; Department of Obstetrics and Gynecology; Key Laboratory of Assisted Reproduction; Ministry of Education; Peking University Third Hospital; Beijing, PR China.

College of Bio-Engineering; Weifang University; Weifang, PR China.

出版信息

Cell Cycle. 2014;13(14):2231-7. doi: 10.4161/cc.29265. Epub 2014 May 28.

Abstract

Gametogenesis is a complex biological process of producing cells for sexual reproduction. Xlr super family members containing a conserved COR1 domain play essential roles in gametogenesis. In the present study, we identified that Slx2, a novel member of Xlr super family, is specifically expressed in the meiotic oocytes, which is demonstrated by western blotting and immunohistochemistry studies. In the first meiotic prophase, SLX2 is unevenly distributed in the nuclei of oocytes, during which phase SLX2 is partly co-localized with SYCP3 in synaptonemal complex and γH2AX in the nucleus of oocytes. Interestingly, the localization of SLX2 was found to be switched into the cytoplasm of oocytes after prometaphase I during oocyte maturation. Furthermore, yeast two-hybrid and coimmunoprecipitation studies demonstrated that SLX2 interacts with BLOS2, which is a novel centrosome-associated protein, and co-localized with γ-Tubulin, which is a protein marker of chromosome segregation in meiosis. These results indicated that SLX2 might get involved in chromosomes segregation during meiosis by interaction with BLOS2. In conclusion, SLX2 might be a novel gametogenesis-related protein that could play multiple roles in regulation of meiotic processes including synaptonemal complex assembly and chromosome segregation.

摘要

配子发生是一个产生用于有性生殖细胞的复杂生物学过程。含有保守COR1结构域的Xlr超家族成员在配子发生中起重要作用。在本研究中,我们鉴定出Xlr超家族的一个新成员Slx2在减数分裂的卵母细胞中特异性表达,这通过蛋白质印迹和免疫组织化学研究得以证实。在第一次减数分裂前期,SLX2在卵母细胞核中分布不均,在此期间SLX2部分与联会复合体中的SYCP3以及卵母细胞核中的γH2AX共定位。有趣的是,在卵母细胞成熟过程中,发现SLX2在中期Ⅰ之后其定位转变到卵母细胞的细胞质中。此外,酵母双杂交和免疫共沉淀研究表明,SLX2与一种新的中心体相关蛋白BLOS2相互作用,并与γ-微管蛋白共定位,γ-微管蛋白是减数分裂中染色体分离的一种蛋白质标志物。这些结果表明,SLX2可能通过与BLOS2相互作用参与减数分裂过程中的染色体分离。总之,SLX2可能是一种新的与配子发生相关的蛋白质,在包括联会复合体组装和染色体分离在内的减数分裂过程调控中可能发挥多种作用。

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