首页> 外文期刊>Journal of Cell Science >The E3 ubiquitin ligase Mib1 regulates Plk4 and centriole biogenesis
【24h】

The E3 ubiquitin ligase Mib1 regulates Plk4 and centriole biogenesis

机译:E3泛素连接酶Mib1调节Plk4和中心粒生物发生

获取原文
获取原文并翻译 | 示例
       

摘要

Centrioles function as core components of centrosomes and as basal bodies for the formation of cilia and flagella. Thus, effective control of centriole numbers is essential for embryogenesis, tissue homeostasis and genome stability. In mammalian cells, the centriole duplication cycle is governed by Polo-like kinase 4 (Plk4). Here, we identify the E3 ubiquitin ligase Mind bomb (Mib1) as a new interaction partner of Plk4. We show that Mib1 localizes to centriolar satellites but redistributes to centrioles in response to conditions that induce centriole amplification. The E3 ligase activity of Mib1 triggers ubiquitylation of Plk4 on multiple sites, causing the formation of Lys11-, Lys29- and Lys48-ubiquitin linkages. These modifications control the abundance of Plk4 and its ability to interact with centrosomal proteins, thus counteracting centriole amplification induced by excess Plk4. Collectively, these results identify the interaction between Mib1 and Plk4 as a new and important element in the control of centriole homeostasis.
机译:着丝粒是着丝粒的核心成分,是纤毛和鞭毛形成的基体。因此,有效控制中心粒数目对于胚胎发生,组织稳态和基因组稳定性至关重要。在哺乳动物细胞中,中心粒复制周期由Polo样激酶4(Plk4)控制。在这里,我们确定E3泛素连接酶Mind炸弹(Mib1)是Plk4的新的相互作用伴侣。我们显示,Mib1定位到中心粒卫星,但在响应诱导中心粒扩增的条件下重新分布到中心粒。 Mib1的E3连接酶活性触发Plk4在多个位点的泛素化,导致Lys11-,Lys29-和Lys48-泛素键的形成。这些修饰控制Plk4的丰度及其与中心体蛋白相互作用的能力,从而抵消了过量Plk4诱导的中心体扩增。总的来说,这些结果确定了Mib1和Plk4之间的相互作用是控制着中心粒稳态的一个新的重要因素。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号