A-type lamin-dependent homo-oligomerization for pY19-Caveolin-2 to function as an insulin-response epigenetic regulator

Biochim Biophys Acta. 2016 Nov;1863(11):2681-2689. doi: 10.1016/j.bbamcr.2016.08.011. Epub 2016 Aug 21.

Abstract

Association of Caveolin-2 in the inner nuclear membrane specifically with A-type lamin is crucial for the maintenance of its Tyr-19 phosphorylation to promote insulin-response epigenetic activation at the nuclear periphery. Here, we identify that pY19-Caveolin-2 in the inner nuclear membrane exists as homo-oligomeric forms and the A-type lamin is required for sustenance of its oligomeric status. Oligomerization-defective and hence pY19-dephosphorylated monomeric Caveolin-2 in the inner nuclear membrane is unable to carry out Caveolin-2-mediated epigenetic activation of Egr-1 and JunB genes and transactivation of Elk-1 and STAT3 in response to insulin. The homo-oligomeric pY19-Caveolin-2 localizes in and recruits epigenetic modifiers to the A-type lamin-enriched inner nuclear membrane microdomain for the epigenetic activation. Our data show that A-type lamin-dependent Caveolin-2 homo-oligomerization in the inner nuclear membrane microdomain is a precondition for pY19-Caveolin-2-mediated insulin-response epigenetic activation at the nuclear periphery.

Keywords: A-type lamin; Caveolin-2; Epigenetic regulators; Homo-oligomerization; Inner nuclear membrane microdomain.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Caveolin 2 / genetics
  • Caveolin 2 / metabolism*
  • Early Growth Response Protein 1 / genetics
  • Early Growth Response Protein 1 / metabolism
  • Epigenesis, Genetic / drug effects*
  • HEK293 Cells
  • Histones / metabolism
  • Humans
  • Insulin / pharmacology*
  • Lamin Type A / genetics
  • Lamin Type A / metabolism*
  • Membrane Microdomains / drug effects
  • Membrane Microdomains / metabolism
  • Nuclear Envelope / drug effects*
  • Nuclear Envelope / metabolism
  • Phosphorylation
  • Protein Binding
  • Protein Interaction Domains and Motifs
  • Protein Transport
  • RNA Interference
  • STAT3 Transcription Factor / genetics
  • STAT3 Transcription Factor / metabolism
  • Signal Transduction / drug effects
  • Transcription Factors / genetics
  • Transcription Factors / metabolism
  • Transcriptional Activation
  • Transfection
  • Tyrosine
  • ets-Domain Protein Elk-1 / genetics
  • ets-Domain Protein Elk-1 / metabolism

Substances

  • Cav2 protein, mouse
  • Caveolin 2
  • EGR1 protein, human
  • ELK1 protein, human
  • Early Growth Response Protein 1
  • Histones
  • Insulin
  • JunB protein, human
  • LMNA protein, human
  • Lamin Type A
  • STAT3 Transcription Factor
  • STAT3 protein, human
  • Transcription Factors
  • ets-Domain Protein Elk-1
  • Tyrosine