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The Anaphase-promoting Complex Coordinates Initiation of Lens Differentiation

机译:晶状体分化的后期促进复数坐标起始

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Lens development requires the precise coordination of cell division and differentiation. The mechanisms by which the differentiation program is initiated after cell cycle arrest remains not well understood. Cyclin-dependent kinase inhibitors (CKIs), such as p15 and p21, have been suggested to be critical components that inhibit G1 progression and therefore, their activation is necessary for quiescence and important for the onset of differentiation. Regulation of p15 and p21 is principally governed by transforming growth factor (TGF)-β–signaling pathway. We have identified that Cdh1/APC, a critical ubiquitin protein ligase, plays an important role in regulating lens differentiation by facilitating TGF-β–induced degradation of SnoN, a transcriptional corepressor that needs to be removed for transcriptional activation of p15 and p21. The depletion of Cdh1 by RNA interference attenuates the TGF-β–mediated induction of p15 and p21 and significantly blocks lens differentiation. Expression of nondegradable SnoN also noticeably attenuates lens induction. Furthermore, we have shown that Cdh1 and SnoN form a complex at the onset of lens differentiation. In vivo histological analysis confirms our biochemical and genetic results. Thus, Cdh1/APC is crucial to the coordination of cell cycle progression and the initiation of lens differentiation through mediating TGF-β–signaling-induced destruction of SnoN.
机译:晶状体发育需要细胞分裂和分化的精确协调。细胞周期停滞后启动分化程序的机制仍不十分清楚。细胞周期蛋白依赖性激酶抑制剂(CKI),例如p15和p21,被认为是抑制G1进程的关键成分,因此,它们的活化对于静止是必需的,并且对于分化的开始很重要。对p15和p21的调节主要受转化生长因子(TGF)-β信号通路的控制。我们已经发现,关键的泛素蛋白连接酶Cdh1 / APC通过促进TGF-β诱导的SnoN的降解而在调节晶状体分化中起重要作用,SnoN是转录共加压因子,需要将其去除才能激活p15和p21的转录。 RNA干扰对Cdh1的消耗会减弱TGF-β介导的p15和p21诱导,并显着阻碍晶状体分化。不可降解SnoN的表达也明显减弱了晶状体的诱导。此外,我们已经表明,Cdh1和SnoN在晶状体分化开始时形成复合物。体内组织学分析证实了我们的生化和遗传结果。因此,Cdh1 / APC通过介导TGF-β信号诱导的SnoN破坏,对协调细胞周期进程和启动晶状体分化至关重要。

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