Identification of FAM96B as a novel prelamin A binding partner

Biochem Biophys Res Commun. 2013 Oct 11;440(1):20-4. doi: 10.1016/j.bbrc.2013.08.099. Epub 2013 Sep 13.

Abstract

Prelamin A accumulation causes nuclear abnormalities, impairs nuclear functions, and eventually promotes cellular senescence. However, the underlying mechanism of how prelamin A promotes cellular senescence is still poorly understood. Here we carried out a yeast two-hybrid screen using a human skeletal muscle cDNA library to search for prelamin A binding partners, and identified FAM96B as a prelamin A binding partner. The interaction of FAM96B with prelamin A was confirmed by GST pull-down and co-immunoprecipitation experiments. Furthermore, co-localization experiments by fluorescent confocal microscopy revealed that FAM96B colocalized with prelamin A in HEK-293 cells. Taken together, our data demonstrated the physical interaction between FAM96B and prelamin A, which may provide some clues to the mechanisms of prelamin A in premature aging.

Keywords: CIA; Cellular senescence; FAM96B; HGPS; Hutchinson–Gilford progeria syndrome; Prelamin A; family with sequence similarity 96 member B; the cytoplasmic Fe–S assembly.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Carrier Proteins / analysis
  • Carrier Proteins / metabolism*
  • Cellular Senescence
  • HEK293 Cells
  • Humans
  • Lamin Type A
  • Metalloproteins
  • Nuclear Proteins / analysis
  • Nuclear Proteins / metabolism*
  • Progeria / metabolism
  • Protein Binding
  • Protein Interaction Maps
  • Protein Precursors / analysis
  • Protein Precursors / metabolism*
  • Two-Hybrid System Techniques

Substances

  • CIAO2B protein, human
  • Carrier Proteins
  • Lamin Type A
  • Metalloproteins
  • Nuclear Proteins
  • Protein Precursors
  • prelamin A