Emerging roles of FAM14 family members (G1P3/ISG 6-16 and ISG12/IFI27) in innate immunity and cancer

J Interferon Cytokine Res. 2011 Jan;31(1):173-81. doi: 10.1089/jir.2010.0105. Epub 2010 Oct 12.

Abstract

Interferons (IFNs) manifest their cellular functions by regulating expression of target genes known collectively as IFN-stimulated genes (ISGs). The repertoires of ISGs vary slightly between cell types, but routinely include a core of common ISGs robustly upregulated in most IFN-treated cells. Here, we review the regulation and cellular functions of 2 related ISGs, ISG12 (IFI27) and G1P3 (ISG 6-16), that are commonly induced by IFNs in most, if not all, IFN-responsive cells. On the basis of sequence similarity, they are grouped together within the newly defined FAM14 family. Emerging data on ISG12 and G1P3 suggest that both are mitochondrial proteins with opposing activities on apoptosis that may influence the innate immune responses of IFNs. The G1P3 gene encodes a low molecular weight mitochondrial protein that may stabilize mitochondrial function and oppose apoptosis. In contrast, ISG12 expression may sensitize cells to apoptotic stimuli via mitochondrial membrane destabilization. On the basis of these results and differences in induction kinetics between ISG12 and G1P3, we have proposed a model for the role of these genes in mediating cellular activity of IFNs.

Publication types

  • Review

MeSH terms

  • Animals
  • Gene Expression Regulation* / drug effects
  • Host-Pathogen Interactions
  • Humans
  • Immunity, Innate* / drug effects
  • Interferons / metabolism*
  • Interferons / pharmacology
  • Membrane Proteins / chemistry
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism*
  • Mitochondrial Proteins / chemistry
  • Mitochondrial Proteins / genetics
  • Mitochondrial Proteins / metabolism*
  • Multigene Family*
  • Neoplasms / metabolism*
  • Phylogeny
  • Protein Interaction Domains and Motifs
  • Protein Transport
  • Virus Diseases / immunology
  • Virus Diseases / metabolism

Substances

  • IFI27 protein, human
  • IFI6 protein, human
  • Membrane Proteins
  • Mitochondrial Proteins
  • Interferons