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由联会复合体蛋白1(SYCP1)募集的两种新蛋白质处于减数分裂的核心。

Two novel proteins recruited by synaptonemal complex protein 1 (SYCP1) are at the centre of meiosis.

作者信息

Costa Yael, Speed Robert, Ollinger Rupert, Alsheimer Manfred, Semple Colin A, Gautier Philippe, Maratou Klio, Novak Ivana, Höög Christer, Benavente Ricardo, Cooke Howard J

机构信息

MRC Human Genetics Unit, Western General Hospital, Edinburgh, UK.

出版信息

J Cell Sci. 2005 Jun 15;118(Pt 12):2755-62. doi: 10.1242/jcs.02402.

Abstract

Completion of meiosis in mammals depends on the formation of the synaptonemal complex, a tripartite structure that physically links homologous chromosomes during prophase I. Several components of the synaptonemal complex are known, including constituents of the cohesin core, the axial/lateral element and the transverse filaments. No protein has previously been identified as an exclusive component of the central element. Mutations in some synaptonemal-complex proteins results in impaired meiosis. In humans, cases of male infertility have been associated with failure to build the synaptonemal complex. To search for new components of the meiotic machinery, we have used data from microarray expression profiling and found two proteins localising solely to the central element of the mammalian synaptonemal complex. These new proteins, SYCE1 and CESC1, interact with the transverse filament protein SYCP1, and their localisation to the central element appears to depend on recruitment by SYCP1. This suggests a role for SYCE1 and CESC1 in synaptonemal-complex assembly, and perhaps also stability and recombination.

摘要

哺乳动物减数分裂的完成依赖于联会复合体的形成,联会复合体是一种在减数第一次分裂前期将同源染色体物理连接起来的三联体结构。已知联会复合体的几个组成部分,包括黏连蛋白核心、轴/侧元件和横向细丝的成分。此前尚未鉴定出任何蛋白质是中央元件的唯一组成部分。一些联会复合体蛋白的突变会导致减数分裂受损。在人类中,男性不育病例与无法构建联会复合体有关。为了寻找减数分裂机制的新成分,我们利用了微阵列表达谱数据,发现了两种仅定位于哺乳动物联会复合体中央元件的蛋白质。这两种新蛋白质SYCE1和CESC1与横向细丝蛋白SYCP1相互作用,它们定位于中央元件似乎依赖于SYCP1的招募。这表明SYCE1和CESC1在联会复合体组装中发挥作用,或许也在其稳定性和重组中发挥作用。

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