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驱动蛋白样蛋白Subito的调控异常在无染色体和中心体的情况下诱导减数分裂纺锤体形成。

Misregulation of the kinesin-like protein Subito induces meiotic spindle formation in the absence of chromosomes and centrosomes.

作者信息

Jang Janet K, Rahman Taslima, Kober Vanessa S, Cesario Jeffry, McKim Kim S

机构信息

Waksman Institute and Department of Genetics, Rutgers, the State University of New Jersey, Piscataway, New Jersey 08854-8020, USA.

出版信息

Genetics. 2007 Sep;177(1):267-80. doi: 10.1534/genetics.107.076091. Epub 2007 Jul 29.

Abstract

Bipolar spindles assemble in the absence of centrosomes in the oocytes of many species. In Drosophila melanogaster oocytes, the chromosomes have been proposed to initiate spindle assembly by nucleating or capturing microtubules, although the mechanism is not understood. An important contributor to this process is Subito, which is a kinesin-6 protein that is required for bundling interpolar microtubules located within the central spindle at metaphase I. We have characterized the domains of Subito that regulate its activity and its specificity for antiparallel microtubules. This analysis has revealed that the C-terminal domain may interact independently with microtubules while the motor domain is required for maintaining the interaction with the antiparallel microtubules. Surprisingly, deletion of the N-terminal domain resulted in a Subito protein capable of promoting the assembly of bipolar spindles that do not include centrosomes or chromosomes. Bipolar acentrosomal spindle formation during meiosis in oocytes may be driven by the bundling of antiparallel microtubules. Furthermore, these experiments have revealed evidence of a nuclear- or chromosome-based signal that acts at a distance to activate Subito. Instead of the chromosomes directly capturing microtubules, signals released upon nuclear envelope breakdown may activate proteins like Subito, which in turn bundles together microtubules.

摘要

在许多物种的卵母细胞中,双极纺锤体在没有中心体的情况下组装。在黑腹果蝇的卵母细胞中,有人提出染色体通过成核或捕获微管来启动纺锤体组装,尽管其机制尚不清楚。这一过程的一个重要促成因素是Subito,它是一种驱动蛋白-6蛋白,在减数分裂I中期捆绑位于中央纺锤体中的极间微管是必需的。我们已经对Subito调节其活性及其对反平行微管特异性的结构域进行了表征。该分析表明,C末端结构域可能独立与微管相互作用,而运动结构域对于维持与反平行微管的相互作用是必需的。令人惊讶的是,N末端结构域的缺失产生了一种能够促进不包括中心体或染色体的双极纺锤体组装的Subito蛋白。卵母细胞减数分裂期间双极无中心体纺锤体的形成可能由反平行微管的捆绑驱动。此外,这些实验揭示了一种基于核或染色体的信号的证据,该信号在远处起作用以激活Subito。不是染色体直接捕获微管,核膜破裂时释放的信号可能激活像Subito这样的蛋白质,进而将微管捆绑在一起。

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