| Literature DB >> 22370726 |
Eun Ju Shin1, Hyun Mi Shin, Eori Nam, Won Seog Kim, Ji-Hoon Kim, Byung-Ha Oh, Yungdae Yun.
Abstract
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.Entities:
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Year: 2012 PMID: 22370726 PMCID: PMC3321169 DOI: 10.1038/embor.2012.3
Source DB: PubMed Journal: EMBO Rep ISSN: 1469-221X Impact factor: 8.807