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首页> 外文期刊>Oncogene >Transcriptional intermediary factor 1γ binds to the anaphase-promoting complex/cyclosome and promotes mitosis
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Transcriptional intermediary factor 1γ binds to the anaphase-promoting complex/cyclosome and promotes mitosis

机译:转录中介因子1γ结合到后期促进复合物/环体,并促进有丝分裂。

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摘要

The anaphase-promoting complex/cyclosome (APC/C) is an ubiquitin ligase that functions during mitosis. Here we identify the transcriptional regulator, transcriptional intermediary factor 1纬, TIF1纬, as an APC/C-interacting protein that regulates APC/C function. TIF1纬 is not a substrate for APC/C-dependent ubiquitylation but instead, associates specifically with the APC/C holoenzyme and Cdc20 to affect APC/C activity and progression through mitosis. RNA interference studies indicate that TIF1纬 knockdown results in a specific reduction in APC/C ubiquitin ligase activity, the stabilization of APC/C substrates, and an increase in the time taken for cells to progress through mitosis from nuclear envelope breakdown to anaphase. TIF1纬 knockdown cells are also characterized by the inappropriate presence of cyclin A at metaphase, and an increase in the number of cells that fail to undergo metaphase-to-anaphase transition. Expression of a small interfering RNA-resistant TIF1纬 species relieves the mitotic phenotype imposed by TIF1纬 knockdown and allows for mitotic progression. Binding studies indicate that TIF1纬 is also a component of the APC/C-mitotic checkpoint complex (MCC), but is not required for MCC dissociation from the APC/C once the spindle assembly checkpoint (SAC) is satisfied. TIF1纬 inactivation also results in chromosome misalignment at metaphase and SAC activation; inactivation of the SAC relieves the mitotic block imposed by TIF1纬 knockdown. Together these data define novel functions for TIF1纬 during mitosis and suggest that a reduction in APC/C ubiquitin ligase activity promotes SAC activation.
机译:后期促进复合物/环体(APC / C)是一种泛素连接酶,在有丝分裂期间起作用。在这里,我们确定转录调节因子,转录中间因子1纬,TIF1纬,作为调节APC / C功能的APC / C相互作用蛋白。 TIF1纬不是APC / C依赖性泛素化的底物,而是与APC / C全酶和Cdc20特异性结合,以影响APC / C活性和有丝分裂进程。 RNA干扰研究表明,TIF1纬敲低可导致APC / C泛素连接酶活性的特定降低,APC / C底物的稳定以及细胞从核被膜破裂到后期的有丝分裂过程所需时间的增加。 TIF1α敲低细胞的特征还在于中期细胞周期蛋白A的不适当存在,以及未能经历中期到后期转变的细胞数量增加。表达小干扰RNA的TIF1纬种可缓解TIF1纬敲低所产生的有丝分裂表型,并允许有丝分裂进程。结合研究表明TIF1纬也是APC / C有丝分裂检查点复合物(MCC)的组成部分,但一旦满足主轴组件检查点(SAC),从APC / C分离MCC并不需要。 TIF1纬失活还会导致中期染色体错位和SAC活化。 SAC的失活缓解了TIF1纬敲除所施加的有丝分裂阻滞。这些数据一起为有丝分裂期间的TIF1纬定义了新功能,并表明APC / C泛素连接酶活性的降低促进了SAC活化。

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