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首页> 外文期刊>Cellular Signalling >NuSAP is degraded by APC/C-Cdh1 and its overexpression results in mitotic arrest dependent of its microtubules' affinity
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NuSAP is degraded by APC/C-Cdh1 and its overexpression results in mitotic arrest dependent of its microtubules' affinity

机译:NuSAP被APC / C-Cdh1降解,其过表达导致有丝分裂停滞,这取决于其微管的亲和力

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摘要

Microtubule associated proteins are involved in regulation of microtubule dynamics. Its mutation and dysregulation result in severe consequences such as mitotic block and apoptosis. NuSAP has been reported as a microtubule associated protein, depletion of which by RNAi results in spindle deficiency and cytokinesis failure. However, its role in regulation of cell cycle and how NuSAP protein is controlled during cell cycle progression still remains unclear. Here we show that NuSAP can be ubiquitinated and degraded by APC/C-hCdh1 E3 ligase. Evolutionally conserved KEN box functions as the degron of NuSAP. Overexpression of NuSAP induces mitotic arrest and the microtubule associated domain and nuclear localization are both required for NuSAP to induce mitotic arrest. Furthermore, overexpression of NuSAP results in cells accumulation with microtubule bundling and spindle deficiency. Thus, our results give evidence for the first time that NuSAP protein level is tightly regulated by the APC/C ubiquitin ligase complex and NuSAP induces mitotic arrest dependent of its microtubule affinity. (c) 2007 Elsevier Inc. All rights reserved.
机译:微管相关蛋白参与微管动力学的调节。其突变和失调导致严重的后果,例如有丝分裂阻滞和细胞凋亡。据报道,NuSAP是一种微管相关蛋白,RNAi对其进行消耗会导致纺锤体缺乏和胞质分裂失败。然而,其在细胞周期调控以及在细胞周期进程中如何控制NuSAP蛋白的作用仍不清楚。在这里,我们显示NuSAP可以被APC / C-hCdh1 E3连接酶泛素化和降解。进化上保守的KEN盒用作NuSAP的德文。 NuSAP的过表达诱导有丝分裂阻滞,并且微管相关结构域和核定位都是NuSAP诱导有丝分裂阻滞所必需的。此外,NuSAP的过表达导致细胞积聚,并伴有微管束和纺锤体缺乏。因此,我们的结果首次证明了NuSAP蛋白水平受到APC / C泛素连接酶复合物的严格调控,并且NuSAP依赖于其微管亲和力诱导有丝分裂停滞。 (c)2007 Elsevier Inc.保留所有权利。

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