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. Author manuscript; available in PMC: 2010 Apr 26.
Published in final edited form as: Mutat Res. 2009 Feb 6;663(1-2):77–83. doi: 10.1016/j.mrfmmm.2009.01.012

Table 2.

Mutational analysis of the CAN1 coding region Wt and rev3 Strainsa

Type of Mutationb Wt
Control
Wt
10 mM Cr(VI)
rev3
Control
rev3
10 mM Cr(VI)
Transitions 75.9% (22) 61.3% (19) 90.0% (36) 82.4% (27)
GC→AT 27.6% (8) 19.4% (6) 32.5% (13) 32.4% (11)
AT→GC 48.3% (14) 41.9% (13) 57.5% (23) 50.0% (17)
Transversions 24.1% (7) 22.6% (7) 10.0% (4) 17.6% (6)
GC→TA 13.8% (3) 6.5% (2) 2.5% (1) 5.9% (2)
GC→CG 3.4 (1) 6.5% (2) 0 0
AT→CG 6.9% (2) 0 0 8.8% (3)
AT→TA 3.4% (1) 9.7% (3) 7.5% (3) 2.9% (1)
Deletions 0 12.9% (4) # 0 0
Insertions 0 3.2 (1) 0 0
a

Data from 10 independent mutant clones for each strain/condition

b

Mutational analysis of CAN1 coding region

Parenthesis indicate the number of mutants

#

Cr(VI)-induced deletions were significantly different from WT control (P=0.052), and rev3 10 mM (P=0.049) yeast.

The mutational spectra generated by Cr(VI) in WT and rev3 yeast were significantly different (P=0.013).