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首页> 外文期刊>Molecular biology of the cell >AgSwe1p Regulates Mitosis in Response to Morphogenesis and Nutrients in Multinucleated Ashbya gossypii Cells
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AgSwe1p Regulates Mitosis in Response to Morphogenesis and Nutrients in Multinucleated Ashbya gossypii Cells

机译:AgSwe1p调节多核Ashbya棉酚细胞的形态发生和营养反应的有丝分裂。

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Nuclei in the filamentous, multinucleated fungus Ashbya gossypii divide asynchronously. We have investigated what internal and external signals spatially direct mitosis within these hyphal cells. Mitoses are most common near cortical septin rings found at growing tips and branchpoints. In septin mutants, mitoses are no longer concentrated at branchpoints, suggesting that the septin rings function to locally promote mitosis near new branches. Similarly, cells lacking AgSwe1p kinase (a Wee1 homologue), AgHsl1p (a Nim1-related kinase), and AgMih1p phosphatase (the Cdc25 homologue that likely counteracts AgSwe1p activity) also have mitoses distributed randomly in the hyphae as opposed to at branchpoints. Surprisingly, however, no phosphorylation of the CDK tyrosine 18 residue, the conserved substrate of Swe1p kinases, was detected in normally growing cells. In contrast, abundant CDK tyrosine phosphorylation was apparent in starving cells, resulting in diminished nuclear density. This starvation-induced CDK phosphorylation is AgSwe1p dependent, and overexpressed AgSwe1p is sufficient to delay nuclei even in rich nutrient conditions. In starving cells lacking septins or AgSwe1p negative regulators, the nuclear density is further diminished compared with wild type. We have generated a model in which AgSwe1p may regulate mitosis in response to cell intrinsic morphogenesis cues and external nutrient availability in multinucleated cells.
机译:丝状,多核真菌Ashbya gossypii中的核异步分裂。我们研究了哪些内部和外部信号在空间上指导这些菌丝细胞内的有丝分裂。线粒体是最常见的在生长尖端和分支点附近的皮质隔膜环上。在septin突变体中,有丝分裂不再集中在分支点,这表明septin环的功能是在新分支附近局部促进有丝分裂。同样,缺乏AgSwe1p激酶(一种Wee1同源物),AgHsl1p(一种与Nim1相关的激酶)和AgMih1p磷酸酶(可能抵消AgSwe1p活性的Cdc25同源物)的细胞也有丝分裂随机分布在菌丝中,而不是在分支点。然而,令人惊讶的是,在正常生长的细胞中未检测到CDK酪氨酸18残基(Swe1p激酶的保守底物)的磷酸化。相反,饥饿的细胞中明显存在大量的CDK酪氨酸磷酸化,导致核密度降低。这种饥饿诱导的CDK磷酸化是AgSwe1p依赖性的,即使在营养丰富的条件下,过表达的AgSwe1p也足以延迟细胞核。在缺乏隔膜或AgSwe1p负调节剂的饥饿细胞中,与野生型相比,核密度进一步降低。我们已经生成了一个模型,其中AgSwe1p可能响应细胞固有的形态发生线索和多核细胞中外部营养的利用而调节有丝分裂。

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