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MSH2 is essential for the preservation of genome integrity and prevents homeologous recombination in the moss Physcomitrella patens

机译:MSH2对于维护基因组完整性至关重要并防止苔藓小立碗藓中的同源重组

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摘要

MSH2 is a central component of the mismatch repair pathway that targets mismatches arising during DNA replication, homologous recombination (HR) and in response to genotoxic stresses. Here, we describe the function of MSH2 in the moss Physcomitrella patens, as deciphered by the analysis of loss of function mutants. Ppmsh2 mutants display pleiotropic growth and developmental defects, which reflect genomic instability. Based on loss of function of the APT gene, we estimated this mutator phenotype to be at least 130 times higher in the mutants than in wild type. We also found that MSH2 is involved in some but not all the moss responses to genotoxic stresses we tested. Indeed, the Ppmsh2 mutants were more tolerant to cisplatin and show higher sensitivity to UV-B radiations. PpMSH2 gene involvement in HR was studied by assessing gene targeting (GT) efficiency with homologous and homeologous sequences. GT efficiency with homologous sequences was slightly decreased in the Ppmsh2 mutant compared with wild type. Strikingly GT efficiency with homeologous sequences decreased proportionally to sequence divergence in the wild type whereas it remained unaffected in the mutants. Those results demonstrate the role of PpMSH2 in the maintenance of genome integrity and in homologous and homeologous recombination.
机译:MSH2是错配修复途径的重要组成部分,其靶向DNA复制,同源重组(HR)以及对遗传毒性胁迫的响应过程中出现的错配。在这里,我们通过功能突变体损失的分析,描述了苔藓小立碗藓中MSH2的功能。 Ppmsh2突变体显示多效性生长和发育缺陷,这反映了基因组的不稳定性。基于APT基因功能的丧失,我们估计该突变体的表型在突变体中比野生型至少高130倍。我们还发现,MSH2参与了我们测试的部分而非全部苔藓对遗传毒性胁迫的反应。实际上,Ppmsh2突变体对顺铂具有更强的耐受性,并且对UV-B辐射显示出更高的敏感性。通过评估同源和同源序列的基因靶向(GT)效率,研究了PpMSH2基因参与HR的过程。与野生型相比,Ppmsh2突变体中具有同源序列的GT效率略有降低。引人注目的是,具有同源序列的GT效率与野生型中的序列差异成比例地降低,而在突变体中却不受影响。这些结果证明了PpMSH2在维持基因组完整性以及同源和同源重组中的作用。

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