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NuSAP a novel microtubule-associated protein involved in mitotic spindle organization

机译:NuSAP一种参与有丝分裂纺锤体组织的新型微管相关蛋白

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摘要

Here, we report on the identification of nucleolar spindle–associated protein (NuSAP), a novel 55-kD vertebrate protein with selective expression in proliferating cells. Its mRNA and protein levels peak at the transition of G2 to mitosis and abruptly decline after cell division. Microscopic analysis of both fixed and live mammalian cells showed that NuSAP is primarily nucleolar in interphase, and localizes prominently to central spindle microtubules during mitosis. Direct interaction of NuSAP with microtubules was demonstrated in vitro. Overexpression of NuSAP caused profound bundling of cytoplasmic microtubules in interphase cells, and this relied on a COOH-terminal microtubule-binding domain. In contrast, depletion of NuSAP by RNA interference resulted in aberrant mitotic spindles, defective chromosome segregation, and cytokinesis. In addition, many NuSAP-depleted interphase cells had deformed nuclei. Both overexpression and knockdown of NuSAP impaired cell proliferation. These results suggest a crucial role for NuSAP in spindle microtubule organization.
机译:在这里,我们报道了核仁纺锤体相关蛋白(NuSAP)的鉴定,NuSAP是一种新型的55 kD脊椎动物蛋白,在增殖细胞中具有选择性表达。它的mRNA和蛋白质水平在G2过渡到有丝分裂时达到峰值,并在细胞分裂后突然下降。固定和活哺乳动物细胞的显微镜分析显示,NuSAP在相间主要是核仁,在有丝分裂期间主要定位于中心纺锤体微管。在体外证明了NuSAP与微管的直接相互作用。 NuSAP的过度表达引起相间细胞中细胞质微管的严重束缚,这依赖于COOH末端微管结合域。相反,RNA干扰耗尽NuSAP会导致有丝分裂纺锤体异常,染色体分离不良和胞质分裂。此外,许多耗尽NuSAP的间期细胞已经使细胞核变形。 NuSAP的过表达和敲低都损害细胞增殖。这些结果表明,NuSAP在纺锤体微管组织中起着至关重要的作用。

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