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. 1997 Sep 16;94(19):10144–10149. doi: 10.1073/pnas.94.19.10144

Table 1.

HPRT mutation rates

Cell line Affected MMR locus* Biochemical deficiency Mutation frequency HPRT mutation rate mutations/generation
HL-60 9.6 ± 3.5 × 10−8 4.7 ± 1.4 × 10−8
HL-60R§ MSH3 amplified hMutSα 2.2 ± 0.9 × 10−4 (+ Mtx) 2.6 ± 1.2 × 10−5 (+ Mtx)
4.4 × 10−4 (no Mtx) 5.0 × 10−5 (no Mtx)
HeLa 1.4 × 10−8 1.0 × 10−8
LoVo MSH2 deletion hMutSα, hMutSβ 3.7 × 10−5 4.9 × 10−6

Mutation rates were determined as described in Materials and Methods. 

*

Mismatch repair (MMR) defect. 

Mutation frequency is expressed as HPRT mutants per colony forming unit (CFU) ± 1 SD. Total CFUs from which 6-thioguanine mutants were selected ranged from 2-10 × 107 cells. 

± One standard deviation. 

§

HL-60R cells were cultured in the presence or absence of 1 μM Mtx as indicated.