Repair bias of large loop mismatches during recombination in mammalian cells depends on loop length and structure

Colin A. Bill , Danielle G. Taghian , Walter A. Duran , Jac A. Nickoloff
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引用次数: 24

Abstract

Repair of loop mismatches was investigated in wild-type and mismatch binding-defective Chinese hamster ovary (CHO) cells. Loop mismatches were formed in vivo during extrachromosomal recombination between heteroallelic plasmid substrates. Recombination was expected to occur primarily by single-strand annealing (SSA), yielding 12- or 26-base nonpalindromic loop mismatches, and 12-, 26-, or 40-base palindromic loop mismatches. Nonpalindromic loops were repaired efficiently and with bias toward loop loss. In contrast, the 12-base palindromic loop was repaired with bias toward loop retention, indicating that repair bias depends on loop structure. Among the palindromic loops, repair bias was dependent on loop length, with bias shifting from loop retention to loop loss with increasing loop size. For both palindromic and nonpalindromic loops, repair efficiencies and biases were independent of the general (MSH/MLH) mismatch repair pathway. These results are discussed with respect to the maintenance of large nonpalindromic insertions, and of small and large palindromes, in eukaryotic genomes.

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哺乳动物细胞重组过程中大环错配的修复偏差取决于环的长度和结构
研究了野生型和错配结合缺陷型中国仓鼠卵巢(CHO)细胞的环错配修复。在体内,在异等位质粒底物之间的染色体外重组过程中形成环错配。重组预计主要通过单链退火(SSA)发生,产生12或26个碱基的非回文环错配,以及12、26或40个碱基的回文环错配。非回文环路修复有效,并倾向于环路损失。相比之下,12碱基回文环的修复偏向于环保留,表明修复偏向于环结构。在回文环路中,修复偏差依赖于环路长度,随着环路大小的增加,偏差从环路保留到环路损失。对于回文和非回文循环,修复效率和偏差与一般(MSH/MLH)错配修复途径无关。这些结果讨论了关于维护大的非回文插入,以及小回文和大回文,在真核生物基因组。
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