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延时显微镜揭示了驱动蛋白在芽殖酵母后期的独特作用。

Time-lapse microscopy reveals unique roles for kinesins during anaphase in budding yeast.

作者信息

Straight A F, Sedat J W, Murray A W

机构信息

Department of Physiology, School of Medicine, University of California San Francisco, San Francisco, California 94143, USA.

出版信息

J Cell Biol. 1998 Nov 2;143(3):687-94. doi: 10.1083/jcb.143.3.687.

Abstract

The mitotic spindle is a complex and dynamic structure. Genetic analysis in budding yeast has identified two sets of kinesin-like motors, Cin8p and Kip1p, and Kar3p and Kip3p, that have overlapping functions in mitosis. We have studied the role of three of these motors by video microscopy of motor mutants whose microtubules and centromeres were marked with green fluorescent protein. Despite their functional overlap, each motor mutant has a specific defect in mitosis: cin8Delta mutants lack the rapid phase of anaphase B, kip1Delta mutants show defects in the slow phase of anaphase B, and kip3Delta mutants prolong the duration of anaphase to the point at which the spindle becomes longer than the cell. The kip3Delta and kip1Delta mutants affect the duration of anaphase, but cin8Delta does not.

摘要

有丝分裂纺锤体是一种复杂且动态的结构。对芽殖酵母的遗传分析已鉴定出两组类驱动蛋白分子马达,即Cin8p和Kip1p,以及Kar3p和Kip3p,它们在有丝分裂中具有重叠功能。我们通过对微管和着丝粒用绿色荧光蛋白标记的驱动蛋白突变体进行视频显微镜观察,研究了其中三种驱动蛋白的作用。尽管它们功能重叠,但每个驱动蛋白突变体在有丝分裂中都有特定缺陷:cin8Δ突变体缺乏后期B的快速阶段,kip1Δ突变体在后期B的缓慢阶段表现出缺陷,而kip3Δ突变体将后期持续时间延长到纺锤体变得比细胞长的程度。kip3Δ和kip1Δ突变体影响后期的持续时间,但cin8Δ不影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e83/2148141/e5f8b66d08ba/JCB9807035.f1a.jpg

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