Di Bacco Alessandra, Gill Grace
Harvard Medical School Department of Pathology, Boston, Massachusetts 02115, USA.
Cell Cycle. 2006 Oct;5(20):2310-3. doi: 10.4161/cc.5.20.3367. Epub 2006 Oct 16.
Post-translational modification by SUMO is a dynamic and reversible process and several SUMO-specific proteases that remove SUMO from substrates have been identified. We have recently described the activities of a new SUMO-specific protease, SENP5. We found that SENP5 discriminates between SUMO-1 and SUMO-2/3 and cells depleted of SENP5 by RNAi failed to proliferate. Our findings support the idea that differential substrate selection by the mammalian SUMO-specific proteases underlies their regulation of distinct biological processes. Furthermore, our finding of a nonredundant function for SENP5 in cell proliferation provides further support for the model that, analogous to phosphorylation, cycles of SUMOylation and deSUMOylation regulate orderly progression through cell division.
小泛素样修饰蛋白(SUMO)介导的翻译后修饰是一个动态且可逆的过程,并且已经鉴定出了几种能从底物上去除SUMO的SUMO特异性蛋白酶。我们最近描述了一种新的SUMO特异性蛋白酶SENP5的活性。我们发现SENP5能区分SUMO-1和SUMO-2/3,并且通过RNA干扰耗尽SENP5的细胞无法增殖。我们的研究结果支持这样一种观点,即哺乳动物SUMO特异性蛋白酶对底物的差异选择是其对不同生物学过程进行调控的基础。此外,我们发现SENP5在细胞增殖中具有非冗余功能,这进一步支持了这样一个模型,即类似于磷酸化,SUMO化和去SUMO化循环调节细胞分裂的有序进程。