首页> 外文期刊>Molecular biology of the cell >The Schizosaccharomyces pombe aurora-related kinase Ark1 interacts with the inner centromere protein Pic1 and mediates chromosome segregation and cytokinesis
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The Schizosaccharomyces pombe aurora-related kinase Ark1 interacts with the inner centromere protein Pic1 and mediates chromosome segregation and cytokinesis

机译:粟酒裂殖酵母极光相关激酶Ark1与内部着丝粒蛋白Pic1相互作用并介导染色体分离和胞质分裂

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摘要

The chromosomal passenger proteins aurora-B, survivin, and inner centromere protein (INCENP) have been implicated in coordinating chromosome segregation with cell division. This work describes the interplay between aurora, survivin, and INCENP orthologs in the fission yeast Schizosaccharomyces pombe and defines their roles in regulating chromosome segregation and cytokinesis. We describe the cloning arid characterization of the aurora-related kinase gene ark1(+), demonstrating that it is an essential gene required for sister chromatid segregation. Cells lacking Ark1p exhibit the cut phenotype, DNA fragmentation, and other defects in chromosome segregation. Overexpression of a kinase-defective version of Ark1, Ark1-K147R, inhibits cytokinesis, with cells exhibiting an elongated, multiseptate phenotype. Ark1p interacts physically and/or genetically with the survivin and INCENP orthologs Bir1p and Pic1p. We identified Pic1p in, a two-hybrid screen for Ark1-K147R interacting partners and went on to map domains in both proteins that mediate their binding. Pic1p residues 925-972 are necessary and sufficient for Ark1p binding, which occurs through the kinase domain. As with Ark1-K147R, overexpression of Ark1p-binding fragments of Pic1p leads to multiseptate phenotypes. We also provide evidence that the dominant-negative effect of Ark1-K147R requires Pic1p binding, indicating that the formation of Ark1p-Pic1p complexes is required for the execution of cytokinesis. [References: 71]
机译:染色体过客蛋白aurora-B,survivin和内部着丝粒蛋白(INCENP)已参与协调染色体分离与细胞分裂。这项工作描述了裂变酵母粟酒裂殖酵母中极光,survivin和INCENP直系同源物之间的相互作用,并定义了它们在调节染色体分离和胞质分裂中的作用。我们描述了极光相关激酶基因ark1(+)的克隆和鉴定,表明它是姐妹染色单体分离所必需的必需基因。缺乏Ark1p的细胞表现出切割的表型,DNA片段化以及染色体分离中的其他缺陷。 Ark1的激酶缺陷型Ark1-K147R的过表达抑制胞质分裂,细胞表现出细长的多肽表型。 Ark1p与survivin和INCENP直系同源物Bir1p和Pic1p发生物理和/或基因相互作用。我们确定了Pic1p,这是Ark1-K147R相互作用伙伴的两个杂交筛选,然后在两个介导其结合的蛋白质中绘制了结构域。 Pic1p残基925-972对通过激酶结构域发生的Ark1p结合是必需的和充分的。与Ark1-K147R一样,Pic1p的Ark1p结合片段的过表达导致多肽表型。我们还提供证据表明,Ark1-K147R的显性负作用需要Pic1p结合,这表明Ark1p-Pic1p复合物的形成是胞质分裂执行所必需的。 [参考:71]

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