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CSAG1 maintains the integrity of the mitotic centrosome in cells with defective p53

机译:CSAG1在具有缺陷P53的细胞中保持有丝分裂中心体的完整性

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摘要

Centrosomes focus microtubules to promote mitotic spindle bipolarity, a critical requirement for balanced chromosome segregation. Comprehensive understanding of centrosome function and regulation requires a complete inventory of components. While many centrosome components have been identified, others yet remain undiscovered. We have used a bioinformatics approach, based on `guilt by association' expression to identify novel mitotic components among the large group of predicted human proteins that have yet to be functionally characterized. Here, we identify chondrosarcoma-associated gene 1 protein (CSAG1) in maintaining centrosome integrity during mitosis. Depletion of CSAG1 disrupts centrosomes and leads to multipolar spindles, particularly in cells with compromised p53 function. Thus, CSAG1may reflect a class of 'mitotic addiction' genes, whose expression is more essential in transformed cells.
机译:CentroSomes焦点微管以促进有丝分裂主轴跨度,这是平衡染色体隔离的关键要求。 全面了解中心功能和监管需要完整的组件库存。 虽然已经确定了许多Centrosome组件,但其他人仍未被发现。 我们使用了生物信息学方法,基于“有罪的关联”表达,以识别尚未在功能表征的大群预测人蛋白中的新型有丝分子组分。 在这里,我们在有丝分裂期间鉴定Chondrosarcoma相关基因1蛋白(CSAG1)保持中心细胞系。 CSAG1的耗尽破坏了CentroSomes并导致多极纺锤,特别是在具有损害的P53功能的细胞中。 因此,CSAG1May反映了一类“有丝分解成瘾”基因,其表达在转化细胞中更为必要。

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