Opposite regulation of F508del-CFTR biogenesis by four poly-lysine ubiquitin chains In vitro

Biochim Biophys Acta Proteins Proteom. 2022 Jun 1;1870(6):140792. doi: 10.1016/j.bbapap.2022.140792. Epub 2022 May 13.

Abstract

As a misfolding protein, almost all of F508del-CFTR is degraded by the ubiquitin-proteasome system before its maturation, which results in no membrane expression of cystic fibrosis transmembrane conductance regulator (CFTR) and therefore, no chloride secretion across epithelial cells of cystic fibrosis (CF) patients. The conjugation of ubiquitin (Ub) chains to protein substrates is necessary for the proteasomal degradation of F508del-CFTR. Ubiquitin contains seven lysine (K) residues, all of which can be conjugated to one another, forming poly-ubiquitin chains on substrates, either by mixing together, or by only one type of lysine providing sorting signals for different pathways. Here, we report that four lysine-linked poly-Ub chains (LLPUCs) were involved in F508del-CFTR biogenesis: LLPUCs linked by K11 or K48 facilitated F508del-CFTR degradation, whereas the other two linked by K63 and K33 protected F508del-CFTR from degradation. LLPUC K11 is more potent for F508del-CFTR degradation than K48. F508del-CFTR utilizes four specific lysine-linked poly-Ub chains during its biogenesis for opposite destiny through different identification by proteasomal shuttle protein or receptors. These findings provide new insights into the CF pathogenesis and are expected to facilitate the development of therapies for this devastating disease.

Keywords: F508del-CFTR; Lysine linked polyubiquitin chain; Proteasomal degradation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cystic Fibrosis Transmembrane Conductance Regulator* / chemistry
  • Cystic Fibrosis Transmembrane Conductance Regulator* / genetics
  • Cystic Fibrosis Transmembrane Conductance Regulator* / metabolism
  • Cystic Fibrosis* / genetics
  • Cystic Fibrosis* / metabolism
  • Cystic Fibrosis* / pathology
  • Humans
  • Lysine
  • Proteasome Endopeptidase Complex / metabolism
  • Ubiquitin

Substances

  • CFTR protein, human
  • Ubiquitin
  • Cystic Fibrosis Transmembrane Conductance Regulator
  • Proteasome Endopeptidase Complex
  • Lysine