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Altered replication and inverted repeats induce mismatch repair-independent recombination between highly diverged DNAs in yeast.

机译:改变的复制和反向重复会诱导酵母中高度分散的DNA之间不匹配修复的重组。

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摘要

Replication, DNA organization, and mismatch repair (MMR) can influence recombination. We examined the effects of altered replication due to a mutation in the polymerase delta gene, long inverted repeats (LIRs) in motifs similar to those in higher eukaryotes, and MMR on intrachromosomal recombination between highly diverged (28%) truncated genes in Saccharomyces cerevisiae. A combination of altered replication and an LIR increased recombination up to 700-fold, while each alone led to a 3- to 20-fold increase. Homeologous recombination was not altered by pms1, msh2, and msh3 mismatch repair mutations. Similar to our previous observations for replication slippage-mediated deletions, there were > or = 5-bp identical runs at the recombination breakpoints. We propose that the dramatic increase in recombination results from enhancement of the effects of altered replication by the LIR, leading to recombinationally active initiating structures. Such interactions predict replication-related, MMR-independent genome changes.
机译:复制,DNA组织和错配修复(MMR)可能影响重组。我们研究了由于聚合酶δ基因突变,与高等真核生物相似的基序中的长反向重复序列(LIR)和MMR对酿酒酵母中高度变异(28%)的截短基因之间的染色体内重组的影响。复制变化和LIR的组合使重组增加了700倍,而单独导致3到20倍的增加。同源重组不会被pms1,msh2和msh3错配修复突变所改变。与我们先前对复制滑移介导的缺失的观察相似,在重组断裂点有≥5 bp的相同序列。我们提出重组的急剧增加是由于增强了LIR改变复制的效果,导致了重组活性的起始结构。这种相互作用预示着复制相关的,MMR独立的基因组变化。

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