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cut11+: A Gene Required for Cell Cycle-dependent Spindle Pole Body Anchoring in the Nuclear Envelope and Bipolar Spindle Formation in Schizosaccharomyces pombe

机译:cut11 +:细胞所需的基因 依赖于循环的主轴极体锚固在核包络中 和裂殖酵母中的双极纺锤体形成 庞贝

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摘要

The “cut” mutants of Schizosaccharomyces pombe are defective in spindle formation and/or chromosome segregation, but they proceed through the cell cycle, resulting in lethality. Analysis of temperature-sensitive alleles of cut11+ suggests that this gene is required for the formation of a functional bipolar spindle. Defective spindle structure was revealed with fluorescent probes for tubulin and DNA. Three-dimensional reconstruction of mutant spindles by serial sectioning and electron microscopy showed that the spindle pole bodies (SPBs) either failed to complete normal duplication or were free floating in the nucleoplasm. Localization of Cut11p tagged with the green fluorescent protein showed punctate nuclear envelope staining throughout the cell cycle and SPBs staining from early prophase to mid anaphase. This SPB localization correlates with the time in the cell cycle when SPBs are inserted into the nuclear envelope. Immunoelectron microscopy confirmed the localization of Cut11p to mitotic SPBs and nuclear pore complexes. Cloning and sequencing showed that cut11+ encodes a novel protein with seven putative membrane-spanning domains and homology to the Saccharomyces cerevisiae gene NDC1. These data suggest that Cut11p associates with nuclear pore complexes and mitotic SPBs as an anchor in the nuclear envelope; this role is essential for mitosis.
机译:粟酒裂殖酵母的“切割”突变体在纺锤体形成和/或染色体分离方面有缺陷,但它们在整个细胞周期中进行,导致致死性。对cut11 +的温度敏感等位基因的分析表明,该基因是功能性双极纺锤体形成所必需的。用微管蛋白和DNA的荧光探针揭示了纺锤体结构的缺陷。通过连续切片和电子显微镜对突变体纺锤体进行三维重建,结果表明纺锤体极体(SPB)不能完成正常的复制或在核质中自由漂浮。用绿色荧光蛋白标记的Cut11p的定位在整个细胞周期中均显示点状核包膜染色,从早期到中期后期都显示SPB染色。 SPB的定位与将SPB插入核被膜中的细胞周期中的时间相关。免疫电子显微镜证实,Cut11p定位于有丝分裂SPB和核孔复合体。克隆和测序表明,cut11 +编码一种新蛋白,具有七个推定的跨膜结构域,并且与酿酒酵母基因NDC1具有同源性。这些数据表明,Cut11p与核孔复合物和有丝分裂SPB缔合,并锚定在核膜中。这个作用对于有丝分裂是必不可少的。

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