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在有丝分裂期将抗Mad2蛋白的抗体显微注射到哺乳动物细胞中会诱导细胞过早进入后期。

Microinjection of antibody to Mad2 protein into mammalian cells in mitosis induces premature anaphase.

作者信息

Gorbsky G J, Chen R H, Murray A W

机构信息

Department of Cell Biology, University of Virginia, Charlottesville, Virginia 22908, USA.

出版信息

J Cell Biol. 1998 Jun 1;141(5):1193-205. doi: 10.1083/jcb.141.5.1193.

Abstract

In yeast, the Mad2 protein is required for the M phase arrest induced by microtubule inhibitors, but the protein is not essential under normal culture conditions. We tested whether the Mad2 protein participates in regulating the timing of anaphase onset in mammalian cells in the absence of microtubule drugs. When microinjected into living prophase or prometaphase PtK1 cells, anti-Mad2 antibody induced the onset of anaphase prematurely during prometaphase, before the chromosomes had assembled at the metaphase plate. Anti-Mad2 antibody-injected cells completed all aspects of anaphase including chromatid movement to the spindle poles and pole-pole separation. Identical results were obtained when primary human keratinocytes were injected with anti-Mad2 antibody. These studies suggest that Mad2 protein function is essential for the timing of anaphase onset in somatic cells at each mitosis. Thus, in mammalian somatic cells, the spindle checkpoint appears to be a component of the timing mechanism for normal mitosis, blocking anaphase onset until all chromosomes are aligned at the metaphase plate.

摘要

在酵母中,Mad2蛋白是微管抑制剂诱导的M期阻滞所必需的,但在正常培养条件下该蛋白并非必不可少。我们测试了在不存在微管药物的情况下,Mad2蛋白是否参与调节哺乳动物细胞后期起始的时间。当将抗Mad2抗体显微注射到活的前期或前中期PtK1细胞中时,在染色体尚未在中期板上组装之前,抗Mad2抗体在前中期过早地诱导了后期的起始。注射了抗Mad2抗体的细胞完成了后期的所有过程,包括染色单体向纺锤体极移动和极间分离。当向原代人角质形成细胞注射抗Mad2抗体时,也获得了相同的结果。这些研究表明,Mad2蛋白功能对于每个有丝分裂中体细胞后期起始的时间至关重要。因此,在哺乳动物体细胞中,纺锤体检查点似乎是正常有丝分裂时间机制的一个组成部分,阻止后期起始直到所有染色体在中期板上排列整齐。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a05f/2137176/e8dea44643a8/JCB9803003.f1.jpg

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