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Mutations in fission yeast Cut15, an importin alpha homolog, lead tomitotic progression without chromosome condensation

机译:裂殖酵母Cut15(一种重要的inletin alpha同源物)中的突变导致无丝分裂的染色体有丝分裂进程

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Chromosome condensation is a major mitotic event [1], Fission yeast mutations in topoisomerase II and condensin subunits produce the characteristic 'cut' phenotypes, in which the septum bisects the nuclear material in the absence of normal condensation and sister chromatid separation [2], We show here that the same condensation defect is produced in cut15 temperature-sensitive mutants at the restrictive temperature (36 degrees C), The gene product of cut15(+) is, surprisingly, very similar to importin alpha [3,4], which binds proteins containing a nuclear localization signal(NLS) and forms the heterodimer with importin beta that mediates translocation through the nuclear pore complex [5]. We show that in a nuclear import assay, purified Cut15 protein behaved identically to mammalian importin a but mutant Cut15 did not. Mutant Cut15 failed to bind an NLS containing protein in vitro but could still bind importin beta. Unexpectedly, however, NLS proteins were imported into the nucleus in cut15 mutants. Cut15 is thus essential for mitotic chromosome condensation, but its role in nuclear import might be dispensable. Green fluorescent protein (GFP) tagged CutlB was enriched within the nucleus specifically during prometaphase-metaphase, so the interaction of Cut15 with nuclear NLS proteins during mitosis might be important for condensation.
机译:染色体凝结是主要的有丝分裂事件[1],拓扑异构酶II和凝缩蛋白亚基中的裂变酵母突变产生特征性的“切割”表型,其中隔膜在没有正常凝结和姐妹染色单体分离的情况下将核物质一分为二[2],我们在这里表明,在极限温度(36摄氏度)下,cut15温度敏感突变体中产生了相同的缩合缺陷。令人惊讶的是,cut15(+)的基因产物与importin alpha [3,4]非常相似。结合含有核定位信号(NLS)的蛋白质,并与importinβ形成异二聚体,后者介导通过核孔复合物的转运[5]。我们显示,在核输入分析中,纯化的Cut15蛋白的行为与哺乳动物的importin相同,但突变体Cut15却没有。突变体Cut15在体外无法结合含有NLS的蛋白质,但仍可以结合importin beta。但是,出乎意料的是,NLS蛋白被导入cut15突变体的细胞核中。因此,Cut15对于有丝分裂染色体的凝聚是必不可少的,但它在核输入中的作用可能是必不可少的。标记有绿色荧光蛋白(GFP)的CutlB在前中期到中期特别是在细胞核内富集,因此在有丝分裂过程中Cut15与核NLS蛋白的相互作用可能对凝结很重要。

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