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Polo 激酶在减数分裂染色体和同源配对所必需的细胞骨架力之间建立联系。

Polo kinases establish links between meiotic chromosomes and cytoskeletal forces essential for homolog pairing.

机构信息

Department of Biology, McGill University, 1205 avenue Docteur Penfield, Montreal, Quebec H2A 1B1, Canada.

出版信息

Dev Cell. 2011 Nov 15;21(5):948-58. doi: 10.1016/j.devcel.2011.07.011. Epub 2011 Oct 20.

Abstract

During meiosis, chromosomes must find and align with their homologous partners. SUN and KASH-domain protein pairs play a conserved role by establishing transient linkages between chromosome ends and cytoskeletal forces across the intact nuclear envelope (NE). In C. elegans, a pairing center (PC) on each chromosome mediates homolog pairing and linkage to the microtubule network. We report that the polo kinases PLK-1 and PLK-2 are targeted to the PC by ZIM/HIM-8-pairing proteins. Loss of plk-2 inhibits chromosome pairing and licenses synapsis between nonhomologous chromosomes, indicating that PLK-2 is required for PC-mediated interhomolog interactions. plk-2 is also required for meiosis-specific phosphorylation of SUN-1 and establishment of dynamic SUN/KASH (SUN-1/ZYG-12) modules that promote homolog pairing. Our results provide key insights into the regulation of homolog pairing and reveal that targeting of polo-like kinases to the NE by meiotic chromosomes establishes the conserved linkages to cytoskeletal forces needed for homology assessment.

摘要

在减数分裂过程中,染色体必须找到并与同源伴侣对齐。SUN 和 KASH 结构域蛋白对通过在完整核膜 (NE) 上建立染色体末端和细胞骨架力之间的瞬时连接,发挥保守作用。在秀丽隐杆线虫中,每个染色体上的配对中心 (PC) 介导同源物配对和与微管网络的连接。我们报告说,极激酶 PLK-1 和 PLK-2 被 ZIM/HIM-8 配对蛋白靶向到 PC。plk-2 的缺失抑制染色体配对,并允许非同源染色体之间的联会,表明 PLK-2 是 PC 介导的交互同源物相互作用所必需的。plk-2 还需要 SUN-1 的减数特异性磷酸化和动态 SUN/KASH(SUN-1/ZYG-12)模块的建立,该模块促进同源物配对。我们的结果提供了同源物配对调控的关键见解,并表明通过减数分裂染色体将 Polo 样激酶靶向到 NE,建立了与同源性评估所需的细胞骨架力的保守连接。

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