Department of Life Science, Ewha Womans University, Seoul 120-750, Korea.
EMBO Rep. 2012 Apr;13(4):339-46. doi: 10.1038/embor.2012.3.
The modification of proteins by small ubiquitin-like modifier (SUMO) is crucial for the regulation of diverse cellular processes. Protein SUMOylation is reversed by isopeptidases, collectively known as deSUMOylases. Only one family of SUMO-specific proteases has been described so far: the sentrin-specific proteases (SENP). Here, we identify and characterize a new deSUMOylase, which we have named DeSI-1 (DeSumoylating Isopeptidase 1). We describe BZEL—a new transcriptional repressor—as substrate of DeSI-1. DeSI-1 catalyses the deSUMOylation, but not the deubiquitination, of BZEL. Furthermore, the SENP substrates PML and ΔNp63 are not deSUMOylated by DeSI-1, suggesting that SENP and DeSI enzymes recognize different sets of substrates. Together, these data identify a second class of SUMO proteases.
蛋白质的小泛素相关修饰物(SUMO)修饰对于调节多种细胞过程至关重要。蛋白质 SUMO 化是由被统称为去 SUMO 酶的异肽酶逆转的。到目前为止,只描述了一个 SUMO 特异性蛋白酶家族:sentrin 特异性蛋白酶(SENP)。在这里,我们鉴定和表征了一种新的去 SUMO 酶,我们将其命名为 DeSI-1(去 SUMO 化异肽酶 1)。我们描述了 BZEL——一种新的转录阻遏物——作为 DeSI-1 的底物。DeSI-1 催化 BZEL 的去 SUMO 化,但不催化去泛素化。此外,SENP 底物 PML 和 ΔNp63 不能被 DeSI-1 去 SUMO 化,这表明 SENP 和 DeSI 酶识别不同的底物。这些数据共同确定了第二类 SUMO 蛋白酶。