Aag-initiated base excision repair drives alkylation-induced retinal degeneration in mice

Proc Natl Acad Sci U S A. 2009 Jan 20;106(3):888-93. doi: 10.1073/pnas.0807030106. Epub 2009 Jan 12.

Abstract

Vision loss affects >3 million Americans and many more people worldwide. Although predisposing genes have been identified their link to known environmental factors is unclear. In wild-type animals DNA alkylating agents induce photoreceptor apoptosis and severe retinal degeneration. Alkylation-induced retinal degeneration is totally suppressed in the absence of the DNA repair protein alkyladenine DNA glycosylase (Aag) in both differentiating and postmitotic retinas. Moreover, transgenic expression of Aag activity restores the alkylation sensitivity of photoreceptors in Aag null animals. Aag heterozygotes display an intermediate level of retinal degeneration, demonstrating haploinsufficiency and underscoring that Aag expression confers a dominant retinal degeneration phenotype.

Publication types

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

MeSH terms

  • Alkylating Agents / toxicity*
  • Animals
  • Apoptosis
  • DNA Glycosylases / physiology*
  • DNA Modification Methylases / physiology
  • DNA Repair Enzymes / physiology
  • DNA Repair*
  • Methyl Methanesulfonate / toxicity
  • Methylnitrosourea / toxicity
  • Mice
  • Photoreceptor Cells, Vertebrate / drug effects
  • Retinal Degeneration / chemically induced*
  • Tumor Suppressor Proteins / physiology

Substances

  • Alkylating Agents
  • Tumor Suppressor Proteins
  • Methylnitrosourea
  • Methyl Methanesulfonate
  • DNA Modification Methylases
  • MGMT protein, mouse
  • 3-methyladenine-DNA glycosylase
  • DNA Glycosylases
  • DNA Repair Enzymes