斯塔斯明
微管
生物
细胞生物学
微管蛋白
磷酸化
有丝分裂
主轴装置
微管聚合
染色质
乙酰化
细胞分裂
遗传学
DNA
细胞
基因
标识
DOI:10.1016/s0955-0674(01)00289-7
摘要
The past several years have seen major advances in our understanding of the mechanisms of microtubule destabilization by oncoprotein18/stathmin (Op18/stathmin) and related proteins. New structural information has clearly shown how members of the Op18/stathmin protein family bind tubulin dimers and suggests models for how these proteins stimulate catastrophe, the transition from microtubule growth to shortening. Regulation of Op18/stathmin by phosphorylation continues to capture much attention. Studies suggest that phosphorylation occurs in a localized fashion, resulting in decreased microtubule destabilizing activity near chromatin or microtubule polymer. A spatial gradient of inactive Op18/stathmin associated with chromatin or microtubules could contribute significantly to mitotic spindle assembly.
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