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. 2001 Aug;21(15):5142–5155. doi: 10.1128/MCB.21.15.5142-5155.2001

TABLE 3.

exo1-dependent mutator genes and mutations identifieda

Mutant strainb Mutator phenotype ratingc EDM gene Nucleotide change Amino acid change
RKY4170 (H9) 5 MLH1 G56A G19D
RKY4171 (H3) 4 MLH1 G82A A28T
RKY4172 (C5) 5 MLH1 G121A A41T
RKY4173 (E15) 4 MLH1 C470T P157L
RKY4174 (C15) 4 MLH1 C680T T227I
RKY4175 (H2) 5 MLH1 G794A R265K
RKY4176 (J2) 5 MLH1 G1640A R547K
RKY4177 (D11) 5 PMS1 C389T A130V
RKY4178 (C14) 4 PMS1 G479A G160D
RKY4179 (F13) 3 PMS1 G913A G305S
RKY4180 (E13) 3 PMS1 C2246T T749I
RKY4181 (C11) 4 PMS1 G2320A D774N
RKY4182 (C2)d 5 PMS1 G2701A D901N
RKY4183 (B9) 4 MSH2 C2285T S762F
RKY4184 (J1) 2 MSH2 G1623A M541I
RKY4185 (D15) 2 MSH3 G2470A G824R
RKY4186 (J10) 3 POL30 G427A E143S
RKY4188 (J3) 3 RNR1 G811T G271S
RKY4187 (I1) 3 POL32 C136T Q46STP
a

The EDM genes were identified by complementation analysis, and then the sequence of each relevant gene was determined. The base and amino acid changes given are numbered assuming that the A of the initiating ATG of each gene is numbered 1. 

b

See Table 2, footnote a

c

The numbers are a qualitative rating of the mutator phenotype of each exo1Δ edmx combination in patch tests like those shown in Fig. 1: 5, complete defect like that seen in an msh2Δ mutant; 4, 75% defect; 3, 50% defect; 2, 25% defect; 1, ∼1% defect like that seen in an exo1Δ mutant; −, wild type. 

d

The phenotype of this mutant was partially suppressed only in the presence of a 2μm plasmid containing EXO1