Ester-linked ubiquitination by HOIL-1 controls immune signalling by shaping the linear ubiquitin landscape

FEBS J. 2021 Oct;288(20):5903-5908. doi: 10.1111/febs.16118. Epub 2021 Jul 28.

Abstract

Ester-linked ubiquitination of serine or threonine residues - or even lipids - has emerged as a new regulatory earmark in cell signalling. Petrova et al. (2021) now reveal that ubiquitin esterification by the atypical ubiquitin ligase HOIL-1, a component of the LUBAC complex, is critical for proper formation of linear ubiquitin chains and control of immune signalling in T cells and macrophages. Surprisingly, ester-linked ubiquitination can either promote or inhibit linear ubiquitin conjugation and cytokine production depending on the receptor and immune cell engaged. Comment on: https://doi.org/10.1111/febs.15896.

Keywords: HOIL-1; LUBAC; immune signalling; inflammation; ubiquitin.

Publication types

  • Research Support, Non-U.S. Gov't
  • Comment

MeSH terms

  • Esters*
  • Signal Transduction
  • Ubiquitin* / metabolism
  • Ubiquitin-Protein Ligases / metabolism
  • Ubiquitination

Substances

  • Esters
  • Ubiquitin
  • Ubiquitin-Protein Ligases