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缺失的 LINC:一种连接有丝分裂染色体和细胞骨架的哺乳动物 KASH 结构域蛋白。

The missing LINC: a mammalian KASH-domain protein coupling meiotic chromosomes to the cytoskeleton.

机构信息

Institute of Medical Biology; Immunos; Singapore.

出版信息

Nucleus. 2014 Jan-Feb;5(1):3-10. doi: 10.4161/nucl.27819. Epub 2014 Jan 23.

Abstract

Pairing of homologous chromosome is a unique event in meiosis that is essential for both haploidization of the genome and genetic recombination. Rapid chromosome movements during meiotic prophase are a key feature of the pairing process. This is usually telomere-led, and in metazoans is dependent upon microtubules and dynein. Chromosome movements culminate in the formation of a meiotic "bouquet" in which nuclear envelope-associated telomeres are clustered at the centrosomal pole of the nucleus. Bouquet formation is thought to facilitate homolog pairing. Recent studies reveal that coupling of telomeres to cytoplasmic dynein is mediated by SUN1 in the inner nuclear membrane (INM) and KASH5 a novel protein of the outer nuclear membrane (ONM). Together SUN1 and KASH5 assemble to form a transluminal LINC (linker of the nucleoskeleton and cytoskeleton) complex that spans both nuclear membranes. SUN1 forms attachment sites for telomeres at the INM while KASH5 functions as a dynein adaptor at the ONM. In mice deficient in KASH5, homologous chromosome pairing does not occur. The result is that meiosis is arrested at the leptotene/zygotene stage of meiotic prophase 1, and as a consequence both male and female mice are infertile. This study demonstrates an essential role for dynein directed telomere movement during meiotic prophase.

摘要

同源染色体的配对是减数分裂中一个独特的事件,对于基因组的单倍体化和遗传重组都是必不可少的。减数分裂前期的染色体快速运动是配对过程的一个关键特征。这通常是端粒引导的,在后生动物中依赖于微管和动力蛋白。染色体运动最终导致减数分裂“花束”的形成,其中核膜相关的端粒聚集在核中心体极。花束的形成被认为有助于同源配对。最近的研究表明,端粒与细胞质动力蛋白的偶联是由核膜内的 SUN1 和核膜外的 KASH5 这两种蛋白介导的。SUN1 和 KASH5 共同组装形成一个贯穿核膜的核骨架和细胞骨架连接(LINC)复合物。SUN1 在核膜内形成端粒的附着位点,而 KASH5 在核膜外作为动力蛋白的接头。在 KASH5 缺失的小鼠中,同源染色体的配对不会发生。结果是减数分裂在减数分裂前期 1 的细线期/合线期停滞,因此雄性和雌性小鼠都不育。这项研究表明,在减数分裂前期,动力蛋白定向的端粒运动起着至关重要的作用。

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