Processive DNA Demethylation via DNA Deaminase-Induced Lesion Resolution

被引:37
作者
Franchini, Don-Marc [1 ,2 ]
Chan, Chun-Fung [3 ]
Morgan, Hugh [3 ]
Incorvaia, Elisabetta [1 ]
Rangam, Gopinath [1 ,2 ]
Dean, Wendy [3 ]
Santos, Fatima [3 ]
Reik, Wolf [3 ,4 ]
Petersen-Mahrt, Svend K. [1 ,2 ]
机构
[1] IFOM Fdn Inst FIRC Oncol Mol, DNA Editing Immun & Epigenet, Milan, Italy
[2] London Res Inst, Clare Hall Labs, DNA Editing Lab, S Mimms, Herts, England
[3] Babraham Inst, Lab Dev Genet & Imprinting, Cambridge, England
[4] Univ Cambridge, Ctr Trophoblast Res, Cambridge, England
基金
英国医学研究理事会; 澳大利亚国家健康与医学研究理事会; 英国生物技术与生命科学研究理事会;
关键词
BASE EXCISION-REPAIR; CLASS SWITCH RECOMBINATION; SINGLE-STRANDED-DNA; SOMATIC HYPERMUTATION; MISMATCH-REPAIR; EPIGENETIC MEMORY; MAMMALIAN-CELLS; AID DEFICIENCY; IN-VITRO; 5-METHYLCYTOSINE;
D O I
10.1371/journal.pone.0097754
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Base modifications of cytosine are an important aspect of chromatin biology, as they can directly regulate gene expression, while DNA repair ensures that those modifications retain genome integrity. Here we characterize how cytosine DNA deaminase AID can initiate DNA demethylation. In vitro, AID initiated targeted DNA demethylation of methyl CpGs when in combination with DNA repair competent extracts. Mechanistically, this is achieved by inducing base alterations at or near methyl-cytosine, with the lesion being resolved either via single base substitution or a more efficient processive polymerase dependent repair. The biochemical findings are recapitulated in an in vivo transgenic targeting assay, and provide the genetic support of the molecular insight into DNA demethylation. This targeting approach supports the hypothesis that mCpG DNA demethylation can proceed via various pathways and mCpGs do not have to be targeted to be demethylated.
引用
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页数:14
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