CIP75 (connexin43-interacting protein of 75 kDa) mediates the endoplasmic reticulum dislocation of connexin43

Vivian Su, Christina Hoang, Dirk Geerts, Alan F Lau

Research output: Contribution to journalArticleAcademicpeer-review


Gap junctions are intercellular channels that comprise connexin proteins such as Cx43 (connexin43). The level of gap junctional intercellular communication can be regulated by Cx43 turnover mediated through various degradation pathways. The UbL (ubiquitin-like) domain-UBA (ubiquitin-associated) domain protein, CIP75 (connexin43-interacting protein of 75 kDa), regulates the proteasomal degradation of Cx43. Subcellular fractionation studies indicated that CIP75 interacts with Cx43 that is localized to the membrane of the ER (endoplasmic reticulum). This Cx43-CIP75 complex also contained the proteasomal subunits S2/Rpn1 and S5a/Rpn10, as demonstrated by co-immunoprecipitation. The deliberate misfolding of Cx43, induced by DTT, led to enhanced CIP75 binding. Reducing CIP75 levels by shRNA-mediated knockdown diminished the association of Cx43 with the proteasome, but still allowed for Cx43 ER dislocation and degradation. These results suggested that CIP75 is essential for the interaction of Cx43 and the proteasome, but that alternate compensatory mechanisms exist to supplement the degradation normally facilitated by CIP75.

Original languageEnglish
Pages (from-to)57-67
Number of pages11
JournalThe Biochemical journal
Issue number1
Publication statusPublished - 15 Feb 2014


  • Connexin 43/metabolism
  • Endoplasmic Reticulum/metabolism
  • HeLa Cells
  • Humans
  • Proteasome Endopeptidase Complex/metabolism
  • Protein Folding

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