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果蝇有丝分裂中的RZZ和Mad1动态变化

RZZ and Mad1 dynamics in Drosophila mitosis.

作者信息

Défachelles Lénaïg, Raich Natacha, Terracol Régine, Baudin Xavier, Williams Byron, Goldberg Michael, Karess Roger E

机构信息

Sorbonne Paris Cité, Université Paris Diderot, Paris, France.

出版信息

Chromosome Res. 2015 Jun;23(2):333-42. doi: 10.1007/s10577-015-9472-x. Epub 2015 Mar 14.

Abstract

The presence or absence of Mad1 at kinetochores is a major determinant of spindle assembly checkpoint (SAC) activity, the surveillance mechanism that delays anaphase onset if one or more kinetochores remain unattached to spindle fibers. Among the factors regulating the levels of Mad1 at kinetochores is the Rod, Zw10, and Zwilch (RZZ) complex, which is required for Mad1 recruitment through a mechanism that remains unknown. The relative dynamics and interactions of Mad1 and RZZ at kinetochores have not been extensively investigated, although Mad1 has been reported to be stably recruited to unattached kinetochores. In this study, we directly compare Mad1-green fluorescent protein (GFP) turnover dynamics on unattached Drosophila kinetochores with that of RZZ, tagged either with GFP-Rod or GFP-Zw10. We find that nearly 40 % of kinetochore-bound Mad1 has a significant dynamic component, turning over with a half-life of 12 s. RZZ in contrast is essentially stable on unattached kinetochores. In addition, we report that a fraction of RZZ and Mad1 can co-immunoprecipitate, indicating that the genetically determined recruitment hierarchy (in which Mad1 depends on RZZ) may reflect a physical association of the two complexes.

摘要

动粒上Mad1的存在与否是纺锤体组装检查点(SAC)活性的主要决定因素,SAC是一种监测机制,若一个或多个动粒未与纺锤体纤维附着,则会延迟后期起始。调节动粒上Mad1水平的因素之一是Rod、Zwilch和Zw10(RZZ)复合体,该复合体通过一种未知机制参与Mad1的募集。尽管有报道称Mad1能稳定募集到未附着的动粒上,但动粒上Mad1与RZZ的相对动力学及相互作用尚未得到广泛研究。在本研究中,我们直接比较了未附着的果蝇动粒上Mad1-绿色荧光蛋白(GFP)的周转动力学与用GFP-Rod或GFP-Zw10标记的RZZ的周转动力学。我们发现,近40%与动粒结合的Mad1具有显著的动态成分,其半衰期为12秒。相比之下,RZZ在未附着的动粒上基本稳定。此外,我们报道一部分RZZ和Mad1可以共同免疫沉淀,这表明基因决定的募集层次结构(其中Mad1依赖于RZZ)可能反映了这两种复合体的物理关联。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eba5/4469085/9a6d62e18c3d/10577_2015_9472_Fig1_HTML.jpg

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