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Mis13磷酸化促進減數(shù)分裂中動粒的組裝
首發(fā)時間:2025-09-12
胡偉(1999),男,主要研究方向:染色體分離機制
劉影 1 2 孫力 1 2 董國琛 1 2 渡邊嘉典 1 2渡邊嘉典,男,教授、博導(dǎo),主要研究方向:染色體分離機制
馬玲玲 1 2 侯海彤 1 2摘要:動粒在進入減數(shù)分裂前期時發(fā)生解體,并在減數(shù)分裂I期之前重新組裝。這一過程的調(diào)控機制及其對減數(shù)分裂的影響還不清楚。本研究發(fā)現(xiàn),在裂殖酵母中Aurora B激酶介導(dǎo)動粒蛋白Mis13的磷酸化,從而調(diào)控減數(shù)分裂中動粒的組裝。在減數(shù)分裂前期,隨著動粒的解體,細胞中觀測不到Mis13-GFP熒光信號點;但在Mis13模擬磷酸化突變體中,能夠觀察到 Mis13-GFP熒光信號點,動粒蛋白Mis12和Nnf1在著絲粒上的定位明顯增強。將細胞阻滯在減數(shù)分裂II的前期時,在Mis13模擬磷酸化突變體中,著絲粒上Mis13-GFP的熒光強度明顯增強;在Mis13去磷酸化突變體中,Mis13-GFP的熒光強度明顯降低。這些結(jié)果說明,Mis13磷酸化促進減數(shù)分裂中動粒的組裝。
關(guān)鍵詞: 減數(shù)分裂 動粒 顯微技術(shù) 動粒解體與組裝 裂殖酵母
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Mis13 Phosphorylation promotes meiotic assembly of kinetochores
胡偉(1999),男,主要研究方向:染色體分離機制
LIU Ying 2 SUN Li 1 DONG Guochen 2 WATANABE Yoshinori 1渡邊嘉典,男,教授、博導(dǎo),主要研究方向:染色體分離機制
MA Lingling 2 HOU Haitong 1Abstract:Kinetochore disassembles during the prophase of meiosis and reassembles before meiosis I. The regulatory mechanism of this process and its impact on meiosis remain unclear. We find that Aurora B kinase mediates the phosphorylation of Mis13, thereby regulating the assembly of kinetochore during meiosis in fission yeast. During prophase of meiosis, Mis13-GFP foci largely disappear along with kinetochore disasseMis13 Phosphorylation promotes meiotic assembly of kinetochoresmbly; however, in the Mis13 phosphomimetic mutant, Mis13-GFP foci can be observed, and the centromeric localization of kinetochore proteins Mis12 and Nnf1 is significantly enhanced. When cells are arrested at the prophase of meiosis II, in the Mis13 phosphomimetic mutant, the intensity of Mis13-GFP foci is significantly enhanced; while in the Mis13 non-phosphorylatable mutant, the intensity of Mis13-GFP is significantly reduced. These results indicate that Mis13 phosphorylation promotes the kinetochore assembly during meiosis.
Keywords: Meiosis Kinetochore Microscopy Kinetochore disassembly and assembly Schizosaccharomyces pombe
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Mis13磷酸化促進減數(shù)分裂中動粒的組裝
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