Endogenous APOBEC3A DNA cytosine deaminase is cytoplasmic and nongenotoxic

J Biol Chem. 2013 Jun 14;288(24):17253-60. doi: 10.1074/jbc.M113.458661. Epub 2013 May 2.

Abstract

APOBEC3A (A3A) is a myeloid lineage-specific DNA cytosine deaminase with a role in innate immunity to foreign DNA. Previous studies have shown that heterologously expressed A3A is genotoxic, suggesting that monocytes may have a mechanism to regulate this enzyme. Indeed, we observed no significant cytotoxicity when interferon was used to induce the expression of endogenous A3A in CD14(+)-enriched primary cells or the monocytic cell line THP-1. In contrast, doxycycline-induced A3A in HEK293 cells caused major cytotoxicity at protein levels lower than those observed when CD14(+) cells were stimulated with interferon. Immunofluorescent microscopy of interferon-stimulated CD14(+) and THP-1 cells revealed that endogenous A3A is cytoplasmic, in stark contrast to stably or transiently transfected A3A, which has a cell-wide localization. A3A constructs engineered to be cytoplasmic are also nontoxic in HEK293 cells. These data combine to suggest that monocytic cells use a cytoplasmic retention mechanism to control A3A and avert genotoxicity during innate immune responses.

Keywords: APOBEC3A; Cytoplasmic Localization; DNA Cytosine Deamination; DNA Damage; Gamma-H2AX; Genotoxicity; HIV; Innate Immunity; Interferon; Monocytes.

Publication types

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

MeSH terms

  • Cell Cycle Proteins / genetics
  • Cell Cycle Proteins / metabolism
  • Cell Survival
  • Cytidine Deaminase / physiology*
  • Cytoplasm / enzymology*
  • DNA Damage*
  • Gene Expression
  • HEK293 Cells
  • Histones / metabolism
  • Humans
  • Immunity, Innate
  • Lipopolysaccharide Receptors / metabolism
  • Monocytes / enzymology
  • Protein Serine-Threonine Kinases / antagonists & inhibitors
  • Protein Serine-Threonine Kinases / genetics
  • Protein Serine-Threonine Kinases / metabolism
  • Proteins / physiology*
  • Repressor Proteins / genetics
  • Repressor Proteins / metabolism

Substances

  • Cell Cycle Proteins
  • H2AX protein, human
  • Histones
  • Lipopolysaccharide Receptors
  • Proteins
  • Repressor Proteins
  • TRIB3 protein, human
  • Protein Serine-Threonine Kinases
  • APOBEC3A protein, human
  • Cytidine Deaminase