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. 2015 Nov 17;44(3):1151–1160. doi: 10.1093/nar/gkv1183

Table 1. ICL-induced mutation spectra in XPA-proficient and -deficient human cells in the presence or absence of HMGB1.

Base substitution Insertion Deletion
XPA+/+ 75% (15/20) 0% (0/20) 25% (5/20)
XPA−/− 75% (15/20) 0% (0/20) 25% (5/20)
HMGB1 KD
XPA+/+ 75% (15/20) 0% (0/20) 45% (9/20)*
XPA−/− 70% (14/20) 5% (1/20) 50% (10/20)*

*Clones containing more than one mutation.

n = 20; mutants sequenced from three independent experiments.

The percentages shown have been calculated as mutations per plasmid sequenced.