DeSUMOylating isopeptidase: A second class of SUMO protease

Eun Ju Shin, Hyun Mi Shin, Eori Nam, Won Seog Kim, Ji Hoon Kim, Byung Ha Oh, Yungdae Yun

Research output: Contribution to journalArticlepeer-review

163 Scopus citations

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.

Original languageEnglish
Pages (from-to)339-346
Number of pages8
JournalEMBO Reports
Volume13
Issue number4
DOIs
StatePublished - Apr 2012

Keywords

  • desumoylation
  • SUMO
  • SUMO-specific protease

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