TABLE 4.
TRD in rad50, mre11, and xrs2 mutant cells
| Genetic background and straina | Median distribution in strains
|
|||
|---|---|---|---|---|
| % Precursor retainedb | Sample size (n) | No. of spore colonies | Pc | |
| Background 1 | ||||
| Wild type | 67 | 14 | 6 | |
| rad50 | 97 | 18 | 7 | <0.01 |
| mre11 | 97 | 6 | 4 | <0.01 |
| Background 2 | ||||
| Wild type | 55 | 13 | 5 | |
| rad50 | 99.2 | 7 | 3 | <0.01 |
| xrs2 | 73 | 8 | 2 | —d |
All strains listed under background 1 were isogenic to W303a. All strains listed under background 2 were derived from a cross between MBH9 and the nonisogenic strain TVL345 or a cross between MBR52-5b and the nonisogenic strain DVL227-6c. TVL345 is isogenic to the DVL227-6c background. Wild-type spore colonies from these crosses were used to determine the wild-type control value.
That is, the percent precursor retained after 20 generations (s2)/the percent precursor present in initial preculture (s0) calculated as described in Materials and Methods.
P values obtained in comparisons between mutant and wild-type strains determined by the rank sum (Mann-Whitney) test.
—, the hypothesis that xrs2 values are identical to wild-type or to rad50 values cannot be rejected at the 95% confidence level by the Mann-Whitney test.