TPR结构域对磷酸化KNL-1的识别将BUB-1-BUB-3复合物定位到优雅小鼠的动点。

Jack Houston, Clémence Vissotsky, Amar Deep, Hiroyuki Hakozaki, Enice Crews, K. Oegema, Kevin D. Corbett, Pablo Lara-Gonzalez, Taekyung Kim, A. Desai
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引用次数: 0

摘要

在有丝分裂过程中,Bub1-Bub3 复合物集中在染色体上的微管耦合界面--动点,在那里它有助于纺锤体检查点的激活、动点-纺锤体微管的相互作用以及中心粒内聚力的保护。Bub1 有一个保守的 N 端四肽重复(TPR)结构域,其后是与其保守互作体 Bub3 的结合基团。目前 Bub1-Bub3 定位于动点的模式是,Bub3 与 Bub1 的结合基团一起识别动点支架蛋白 Knl1 中的磷酸化 "MELT "基团。在秀丽隐杆线虫中,BUB-1 和 BUB-3 的缺失在表型上更为严重,受此影响,我们发现 BUB-1 的 TPR 结构域能直接识别 KNL-1 中的一类不同的磷酸化基团,而且这种相互作用对于 BUB-1-BUB-3 的定位和功能至关重要。BUB-3对磷酸化-MELT基团的识别在有丝分裂进入过程中对驱动BUB-1-BUB-3在其KNL-1支架上的超定量积累起到了加成作用。在其他物种中,Bub1的TPR结构域与Knl1相互作用,这表明在Bub1-Bub3的定位和功能中,依赖于TPR的界面和依赖于Bub3的界面之间的协作可能是保守的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Phospho-KNL-1 recognition by a TPR domain targets the BUB-1-BUB-3 complex to C. elegans kinetochores.
During mitosis, the Bub1-Bub3 complex concentrates at kinetochores, the microtubule-coupling interfaces on chromosomes, where it contributes to spindle checkpoint activation, kinetochore-spindle microtubule interactions, and protection of centromeric cohesion. Bub1 has a conserved N-terminal tetratricopeptide repeat (TPR) domain followed by a binding motif for its conserved interactor Bub3. The current model for Bub1-Bub3 localization to kinetochores is that Bub3, along with its bound motif from Bub1, recognizes phosphorylated "MELT" motifs in the kinetochore scaffold protein Knl1. Motivated by the greater phenotypic severity of BUB-1 versus BUB-3 loss in C. elegans, we show that the BUB-1 TPR domain directly recognizes a distinct class of phosphorylated motifs in KNL-1 and that this interaction is essential for BUB-1-BUB-3 localization and function. BUB-3 recognition of phospho-MELT motifs additively contributes to drive super-stoichiometric accumulation of BUB-1-BUB-3 on its KNL-1 scaffold during mitotic entry. Bub1's TPR domain interacts with Knl1 in other species, suggesting that collaboration of TPR-dependent and Bub3-dependent interfaces in Bub1-Bub3 localization and functions may be conserved.
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