van Leuken Renske J, Luna-Vargas Mark P, Sixma Titia K, Wolthuis Rob M F, Medema René H
Department of Medical Oncology, University Medical Center Utrecht, Utrecht, The Netherlands.
Cell Cycle. 2008 Sep 1;7(17):2710-9. doi: 10.4161/cc.7.17.6553. Epub 2008 Sep 3.
Accurate chromosome segregation relies on the mitotic spindle checkpoint. This checkpoint acts to restrict ubiquitin ligase activity of the Anaphase-promoting complex (APC/C) in mitosis until all chromosomes are bipolarly attached to the mitotic spindle. We performed a functional RNAi-based screen to identify De-ubiquitinating enzymes (Dubs) involved in mitotic progression. We identified Usp39 as a new factor required to maintain the spindle checkpoint and support successful cytokinesis. Strikingly, although Usp39 clearly contains an ubiquitin-protease domain, we show that Usp39 is entirely deprived of Dub activity. However, consistent wilt a previously described role for Usp39 in mRNA processing, we observed specific reduction in Aurora B-mRNA levels after depletion of Usp39. Although we find that exogenously expressed Aurora B cDNA is not sufficient to rescue the checkpoint defect of Usp39-depleted cells, Aurora B expression is restored. Our observations suggest Usp39 to be involved in splicing of Aurora B and other mRNAs that are essential for proper spindle checkpoint function.
精确的染色体分离依赖于有丝分裂纺锤体检查点。该检查点在有丝分裂过程中发挥作用,限制后期促进复合物(APC/C)的泛素连接酶活性,直到所有染色体都双极附着于有丝分裂纺锤体。我们进行了一项基于RNA干扰的功能筛选,以鉴定参与有丝分裂进程的去泛素化酶(Dubs)。我们确定Usp39是维持纺锤体检查点和支持成功胞质分裂所需的一个新因子。令人惊讶的是,尽管Usp39明显含有一个泛素蛋白酶结构域,但我们发现Usp39完全没有去泛素化酶活性。然而,与之前描述的Usp39在mRNA加工中的作用一致,我们观察到Usp39缺失后Aurora B-mRNA水平出现特异性降低。虽然我们发现外源表达的Aurora B cDNA不足以挽救Usp39缺失细胞的检查点缺陷,但Aurora B的表达得以恢复。我们的观察结果表明,Usp39参与了Aurora B和其他对纺锤体检查点正常功能至关重要的mRNA的剪接。