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裂殖酵母nuc2突变体细胞中纺锤体伸长的体外再激活。

In vitro reactivation of spindle elongation in fission yeast nuc2 mutant cells.

作者信息

Masuda H, Hirano T, Yanagida M, Cande W Z

机构信息

Department of Molecular and Cell Biology, University of California, Berkeley 94720.

出版信息

J Cell Biol. 1990 Feb;110(2):417-25. doi: 10.1083/jcb.110.2.417.

Abstract

To investigate the mechanisms of spindle elongation and chromosome separation in the fission yeast Schizosaccharomyces pombe, we have developed an in vitro assay using a temperature-sensitive mutant strain, nuc2. At the restrictive temperature, nuc2 cells are arrested at a metaphase-like stage with short spindles and condensed chromosomes. After permeabilization of spheroplasts of the arrested cells, spindle elongation was reactivated by addition of ATP and neurotubulin both at the restrictive and the permissive temperatures, but chromosome separation was not. This suggests that the nuc2 cells are impaired in function at a stage before sister chromatid disjunction. Spindle elongation required both ATP and exogenous tubulin and was inhibited by adenylyl imidodiphosphate (AMPPNP) or vanadate. The ends of yeast half-spindle microtubules pulse-labeled with biotinylated tubulin moved past each other during spindle elongation and a gap formed between the original half-spindles. These results suggest that the primary mechanochemical event responsible for spindle elongation is the sliding apart of antiparallel microtubules of the two half-spindles.

摘要

为了研究裂殖酵母粟酒裂殖酵母中纺锤体伸长和染色体分离的机制,我们利用温度敏感突变株nuc2开发了一种体外试验。在限制温度下,nuc2细胞停滞在类似中期的阶段,纺锤体短,染色体浓缩。在对停滞细胞的原生质球进行通透处理后,在限制温度和允许温度下,通过添加ATP和神经微管蛋白都能重新激活纺锤体伸长,但染色体分离不能被激活。这表明nuc2细胞在姐妹染色单体分离前的一个阶段功能受损。纺锤体伸长需要ATP和外源微管蛋白,并被腺苷酰亚胺二磷酸(AMPPNP)或钒酸盐抑制。用生物素化微管蛋白脉冲标记的酵母半纺锤体微管的末端在纺锤体伸长过程中相互移动,并且在原来的半纺锤体之间形成了一个间隙。这些结果表明,负责纺锤体伸长的主要机械化学事件是两个半纺锤体的反平行微管相互滑动。

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