Proteasome-mediated degradation of integral inner nuclear membrane protein emerin in fibroblasts lacking A-type lamins

Biochem Biophys Res Commun. 2006 Dec 29;351(4):1011-7. doi: 10.1016/j.bbrc.2006.10.147. Epub 2006 Nov 3.

Abstract

We previously identified and characterized a homozygous LMNA nonsense mutation leading to the absence of A-type lamins in a premature neonate who died at birth. We show here that the absence of A-type lamins is due to degradation of the aberrant mRNA transcript with a premature termination codon. In cultured fibroblasts from the subject with the homozygous LMNA nonsense mutation, there was a decreased steady-state expression of the integral inner nuclear membrane proteins emerin and nesprin-1alpha associated with their mislocalization to the bulk endoplasmic reticulum and a hyperphosphorylation of emerin. To determine if decreased emerin expression occurred post-translationally, we treated cells with a selective proteasome inhibitor and observed an increase in expression. Our results show that mislocalization of integral inner nuclear membrane proteins to the endoplasmic reticulum in human cells lacking A-type lamins leads to their degradation and provides the first evidence that their degradation is mediated by the proteasome.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cells, Cultured
  • Child
  • Endoplasmic Reticulum / chemistry
  • Endoplasmic Reticulum / metabolism*
  • Fibroblasts / metabolism*
  • Fibroblasts / ultrastructure
  • Homozygote
  • Humans
  • Lamin Type A / analysis
  • Lamin Type A / deficiency*
  • Lamin Type A / genetics
  • Male
  • Membrane Proteins / analysis
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism*
  • Mutation
  • Nuclear Envelope / metabolism
  • Nuclear Proteins / analysis
  • Nuclear Proteins / genetics
  • Nuclear Proteins / metabolism*
  • Proteasome Endopeptidase Complex / metabolism*
  • RNA, Messenger / analysis
  • RNA, Messenger / metabolism
  • Skin / cytology
  • Skin / metabolism

Substances

  • Lamin Type A
  • Membrane Proteins
  • Nuclear Proteins
  • RNA, Messenger
  • emerin
  • Proteasome Endopeptidase Complex