Dohet C, Dzidić S, Wagner R, Radman M
Mol Gen Genet. 1987 Jan;206(1):181-4. doi: 10.1007/BF00326556.
Unmethylated DNA heteroduplexes with a large single stranded loop in one strand have been prepared from separated strands of DNA from two different strains of bacteriophage lambda, one of which has a approximately 800 base pair IS1 insertion in the cI gene. The results of transfections with these heteroduplexes into wild-type and mismatch repair deficient bacteria indicate that such large non-homologies are not repaired by the Escherichia coli mismatch repair system. However, the results do suggest that some process can act to repair such large non-homologies in heteroduplex DNA. Transfections of a series of recombination and excision repair deficient mutants suggest that known excision or recombination repair systems of E. coli are not responsible for the repair. Repair of large non-homologies may play a role in gene conversion involving large insertion or deletion mutations.
已从两种不同的λ噬菌体菌株的分离DNA链制备出在一条链上带有大的单链环的未甲基化DNA异源双链体,其中一种在cI基因中有大约800个碱基对的IS1插入。将这些异源双链体转染到野生型和错配修复缺陷型细菌中的结果表明,大肠杆菌错配修复系统不会修复这种大的非同源性。然而,结果确实表明某些过程可以修复异源双链DNA中的这种大的非同源性。一系列重组和切除修复缺陷型突变体的转染表明,大肠杆菌已知的切除或重组修复系统与这种修复无关。大的非同源性的修复可能在涉及大的插入或缺失突变的基因转换中起作用。