Shcherbakov V P, Plugina L A, Kudryashova E A, Efremova O I, Sizova S T, Toompuu O G
Genetics. 1982 Dec;102(4):627-37. doi: 10.1093/genetics/102.4.627.
The contribution of mismatch repair to genetic recombination in T4 phage has been evaluated by three independent approaches: (1) testing for non-additivity of recombinant frequencies; (2) measurements of double exchange frequencies in three-factor crosses: (3) comparisons of recombination abilities of mutations occupying the same site. Quantitative agreement among the results of these approaches suggests that within distances much less than the mean length of hybrid regions, mismatch repair accounts perfectly for high negative interference as measured in three-factor crosses and as manifested by non-additivity in two-factor crosses. The mismatch repair mechanism readily recognizes only particular mismatches, the repair frequency being dependent on the base sequence in both strands of the mismatched region.
错配修复对T4噬菌体基因重组的贡献已通过三种独立方法进行评估:(1)检测重组频率的非加和性;(2)测量三因子杂交中的双交换频率;(3)比较占据同一位点的突变的重组能力。这些方法的结果在数量上的一致性表明,在远小于杂种区域平均长度的距离内,错配修复完全解释了三因子杂交中所测量到的高负干扰以及双因子杂交中表现出的非加和性。错配修复机制仅能轻易识别特定的错配,修复频率取决于错配区域两条链中的碱基序列。