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有证据表明Ipl1-Sli15(极光激酶-内着丝粒蛋白复合体)通过改变动粒-纺锤体极连接来促进染色体双定向。

Evidence that the Ipl1-Sli15 (Aurora kinase-INCENP) complex promotes chromosome bi-orientation by altering kinetochore-spindle pole connections.

作者信息

Tanaka Tomoyuki U, Rachidi Najma, Janke Carsten, Pereira Gislene, Galova Marta, Schiebel Elmar, Stark Michael J R, Nasmyth Kim

机构信息

School of Life Sciences, University of Dundee, MSI/WTB complex, DD1 5EH, Dundee, United Kingdom.

出版信息

Cell. 2002 Feb 8;108(3):317-29. doi: 10.1016/s0092-8674(02)00633-5.

Abstract

How sister kinetochores attach to microtubules from opposite spindle poles during mitosis (bi-orientation) remains poorly understood. In yeast, the ortholog of the Aurora B-INCENP protein kinase complex (Ipl1-Sli15) may have a role in this crucial process, because it is necessary to prevent attachment of sister kinetochores to microtubules from the same spindle pole. We investigated IPL1 function in cells that cannot replicate their chromosomes but nevertheless duplicate their spindle pole bodies (SPBs). Kinetochores detach from old SPBs and reattach to old and new SPBs with equal frequency in IPL1+ cells, but remain attached to old SPBs in ipl1 mutants. This raises the possibility that Ipl1-Sli15 facilitates bi-orientation by promoting turnover of kinetochore-SPB connections until traction of sister kinetochores toward opposite spindle poles creates tension in the surrounding chromatin.

摘要

在有丝分裂期间,姐妹动粒如何附着于来自纺锤体两极相对的微管(双定向)仍知之甚少。在酵母中,Aurora B-INCENP蛋白激酶复合体(Ipl1-Sli15)的直系同源物可能在这一关键过程中发挥作用,因为它对于防止姐妹动粒附着于来自同一纺锤体极的微管是必需的。我们研究了IPL1在无法复制其染色体但仍能复制其纺锤体极体(SPB)的细胞中的功能。在IPL1+细胞中,动粒以相同频率从旧的SPB上脱离并重新附着于旧的和新的SPB,但在ipl1突变体中,动粒仍附着于旧的SPB。这增加了一种可能性,即Ipl1-Sli15通过促进动粒-SPB连接的周转来促进双定向,直到姐妹动粒向相反纺锤体极的牵引在周围染色质中产生张力。

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