Abstract
Begum et al.(6) argue that UNG catalytic activity cannot be involved in the formation of DSBs because, when they ectopically expressed three catalytically crippled forms of UNG in UNG–/– B cells, DSBs and overall CSR were observed [UNG–/– B cells have previously been found deficient in the formation of DSBs and CSR (7).]. However, the three UNG single mutants—D145N, N204V, and H268L—are still very powerful catalysts and can excise uracil from duplex DNA with a half-life of about 1 min (8, 9). This residual activity may be sufficient to give rise to DSBs at a rate comparable to, or faster than, the subsequent steps in CSR.