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GADD45? inhibition of DNMT1 dependent DNA methylation during homology directed DNA repair.


ABSTRACT: In this work, we examine regulation of DNA methyltransferase 1 (DNMT1) by the DNA damage inducible protein, GADD45?. We used a system to induce homologous recombination (HR) at a unique double-strand DNA break in a GFP reporter in mammalian cells. After HR, the repaired DNA is hypermethylated in recombinant clones showing low GFP expression (HR-L expressor class), while in high expressor recombinants (HR-H clones) previous methylation patterns are erased. GADD45?, which is transiently induced by double-strand breaks, binds to chromatin undergoing HR repair. Ectopic overexpression of GADD45? during repair increases the HR-H fraction of cells (hypomethylated repaired DNA), without altering the recombination frequency. Conversely, silencing of GADD45? increases methylation of the recombined segment and amplifies the HR-L expressor (hypermethylated) population. GADD45? specifically interacts with the catalytic site of DNMT1 and inhibits methylation activity in vitro. We propose that double-strand DNA damage and the resulting HR process involves precise, strand selected DNA methylation by DNMT1 that is regulated by GADD45?. Since GADD45? binds with high avidity to hemimethylated DNA intermediates, it may also provide a barrier to spreading of methylation during or after HR repair.

SUBMITTER: Lee B 

PROVIDER: S-EPMC3315326 | biostudies-literature | 2012 Mar

REPOSITORIES: biostudies-literature

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GADD45α inhibition of DNMT1 dependent DNA methylation during homology directed DNA repair.

Lee Bongyong B   Morano Annalisa A   Porcellini Antonio A   Muller Mark T MT  

Nucleic acids research 20111201 6


In this work, we examine regulation of DNA methyltransferase 1 (DNMT1) by the DNA damage inducible protein, GADD45α. We used a system to induce homologous recombination (HR) at a unique double-strand DNA break in a GFP reporter in mammalian cells. After HR, the repaired DNA is hypermethylated in recombinant clones showing low GFP expression (HR-L expressor class), while in high expressor recombinants (HR-H clones) previous methylation patterns are erased. GADD45α, which is transiently induced by  ...[more]

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