Article
Pms2 and uracil-DNA glycosylases act jointly in the mismatch repair pathway to generate Ig gene mutations at A-T base pairs.
The Journal of experimental medicine - 3 Apr 2017
Girelli Zubani Giulia, Zivojnovic Marija, De Smet Annie, Albagli-Curiel Olivier, Huetz François, Weill Jean-Claude, Reynaud Claude-Agnès, Storck Sébastien
Abstract excerpt
During somatic hypermutation (SHM) of immunoglobulin genes, uracils introduced by activation-induced cytidine deaminase are processed by uracil-DNA glycosylase (UNG) and mismatch repair (MMR) pathways to generate mutations at G-C and A-T base pairs, respectively. Paradoxically, the MMR-nicking complex Pms2/Mlh1 is apparently dispensable for A-T mutagenesis. Thus, how detection of U:G mismatches is translated into...
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