4.6 Article

An N-terminal SIAH-interacting motif regulates the stability of the ubiquitin specific protease (USP)-19

期刊

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.bbrc.2013.02.094

关键词

USP19; SIAH1 ligase; SIAH degron; Proteasomal degradation

资金

  1. Karolinska Institutet
  2. Ake Wibergs Stiftelse
  3. Swedish Research Council
  4. Magnus Bergvalls Stiftelse
  5. ERACOL

向作者/读者索取更多资源

The Ubiquitin Specific Protease-19 (USP19) regulates cell cycle progression and is involved in the cellular response to different types of stress, including the unfolded protein response (UPR), hypoxia and muscle atrophy. Using the unique N-terminal domain as bait in a yeast-two hybrid screen we have identified the ubiquitin ligases Seven In Absentia Homolog (SIAH)-1 and SIAH2 as binding partners of USP19. The interaction is mediated by a SIAH-consensus binding motif and promotes USP19 ubiquitylation and proteasome-dependent degradation. These findings identify USP19 as a common substrate of the SIAH ubiquitin ligases. (C) 2013 Elsevier Inc. All rights reserved.

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