Humbert O, Prudhomme M, Hakenbeck R, Dowson C G, Claverys J P
Centre National de la Recherche Scientifique-Unité Propre de Recherche 9007, Université Paul Sabatier, Tolouse, France.
Proc Natl Acad Sci U S A. 1995 Sep 26;92(20):9052-6. doi: 10.1073/pnas.92.20.9052.
The ability of the Hex generalized mismatch repair system to prevent recombination between partially divergent (also called homeologous) sequences during transformation in Streptococcus pneumoniae was investigated. By using as donor in transformation cloned fragments 1.7-17.5% divergent in DNA sequence from the recipient, it was observed that the Hex system prevents chromosomal integration of the least and the most divergent fragments but frequently fails to do so for other fragments. In the latter case, the Hex system becomes saturated (inhibited) due to an excess of mismatches: it is unable to repair a single mismatch located elsewhere on the chromosome. Further investigation with chromosomal donor DNA, carrying only one genetically marked divergent region, revealed that a single divergent fragment can lead to saturation of the Hex system. Increase in cellular concentration of either HexA, the MutS homologue that binds mismatches, or HexB, the MutL homologue for which the essential role in repair as yet remains obscure, was shown to restore repair ability in previously saturating conditions. Investigation of heterospecific transformation by chromosomal DNA from two related streptococcal species, Streptococcus oralis and Streptococcus mitis, also revealed complete saturation of the Hex system. Therefore the Hex system is not a barrier to interspecies recombination in S. pneumoniae. These results are discussed in light of those described for the Mut system of Escherichia coli.
研究了六聚体广义错配修复系统在肺炎链球菌转化过程中阻止部分差异(也称为同源)序列之间重组的能力。通过在转化中使用与受体DNA序列有1.7 - 17.5%差异的克隆片段作为供体,观察到六聚体系统阻止了差异最小和最大的片段进行染色体整合,但对于其他片段常常无法做到这一点。在后一种情况下,六聚体系统由于错配过多而饱和(受抑制):它无法修复位于染色体其他位置的单个错配。对仅携带一个基因标记差异区域的染色体供体DNA进行的进一步研究表明,单个差异片段可导致六聚体系统饱和。结果显示,增加与错配结合的MutS同源物HexA或在修复中基本作用仍不清楚的MutL同源物HexB的细胞浓度,可在先前饱和的条件下恢复修复能力。对来自两个相关链球菌物种——口腔链球菌和缓症链球菌的染色体DNA进行的异种特异性转化研究也显示六聚体系统完全饱和。因此,六聚体系统不是肺炎链球菌种间重组的障碍。将根据针对大肠杆菌Mut系统所描述的结果对这些结果进行讨论。