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CDC-48/p97 通过控制线虫中 AIR-2/Aurora B 激酶的定位,对减数分裂染色体的正确分离是必需的。

CDC-48/p97 is required for proper meiotic chromosome segregation via controlling AIR-2/Aurora B kinase localization in Caenorhabditis elegans.

机构信息

Department of Molecular Cell Biology, Institute of Molecular Embryology and Genetics, Kumamoto University, 2-2-1 Honjo, Kumamoto 860-0811, Japan.

出版信息

J Struct Biol. 2012 Aug;179(2):104-11. doi: 10.1016/j.jsb.2012.06.009. Epub 2012 Jun 23.

Abstract

CDC-48/p97 is a AAA (ATPases associated with diverse cellular activities) chaperone involved in protein conformational changes such as the disassembly of protein complexes. We previously reported that Caenorhabditis elegans CDC-48.1 and CDC-48.2 (CDC-48s) are essential for the progression of meiosis I metaphase. Here, we report that CDC-48s are required for proper chromosome segregation during meiosis in C. elegans. In wild-type worms, at the diakinesis phase, phosphorylation of histone H3, one of the known substrates of aurora B kinase (AIR-2), on meiosis I chromatids correlated with AIR-2 localization at the cohesion sites of homologous chromatids. Conversely, depletion of CDC-48s resulted in a significant expansion of signals for AIR-2 and phosphorylated histone H3 over the entire length of meiotic chromosomes, leading to defective chromosome segregation, while the total amount of AIR-2 in lysates was not changed by the depletion of CDC-48s. The defective segregation of meiotic chromosomes caused by the depletion of CDC-48s was suppressed by the simultaneous depletion of AIR-2 and is similar to that observed following the depletion of protein phosphatase 1 (PP1) phosphatases. However, the amount and localization of PP1 were not changed by the depletion of CDC-48s. These results suggest that CDC-48s control the restricted localization of AIR-2 to the cohesion sites of homologous chromatids in meiosis I.

摘要

CDC-48/p97 是一种 AAA(与多种细胞活动相关的 ATP 酶)伴侣,参与蛋白质构象变化,如蛋白质复合物的解体。我们之前报道过,秀丽隐杆线虫的 CDC-48.1 和 CDC-48.2(CDC-48s)对于减数分裂 I 中期的进展是必不可少的。在这里,我们报告 CDC-48s 对于线虫减数分裂过程中的正确染色体分离是必需的。在野生型蠕虫中,在减数分裂前期,组蛋白 H3 的磷酸化,已知的极光 B 激酶(AIR-2)的底物之一,与 AIR-2 在同源染色单体的着丝粒处的定位相关。相反,CDC-48s 的耗竭导致 AIR-2 和磷酸化组蛋白 H3 的信号在整个减数分裂染色体长度上显著扩展,导致染色体分离缺陷,而 CDC-48s 耗竭对裂解物中 AIR-2 的总量没有影响。CDC-48s 耗竭导致的减数分裂染色体分离缺陷可以通过同时耗竭 AIR-2 和蛋白磷酸酶 1(PP1)磷酸酶来抑制。然而,CDC-48s 的耗竭并没有改变 PP1 的数量和定位。这些结果表明,CDC-48s 控制 AIR-2 在减数分裂 I 中同源染色单体着丝粒处的限制定位。

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