Skip to main navigation Skip to search Skip to main content

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
  • Ewha Womans University
  • Sungkyunkwan University
  • Korea Advanced Institute of Science and Technology

Research output: Contribution to journalArticlepeer-review

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
Externally publishedYes

Keywords

  • SUMO
  • SUMO-specific protease
  • desumoylation

Fingerprint

Dive into the research topics of 'DeSUMOylating isopeptidase: A second class of SUMO protease'. Together they form a unique fingerprint.

Cite this