Evolutionary implications of the frequent horizontal transfer of mismatch repair genes

被引:192
作者
Denamur, E
Lecointre, G
Darlu, P
Tenaillon, O
Acquaviva, C
Sayada, C
Sunjevaric, I
Rothstein, R
Elion, J
Taddei, F
Radman, M
Matic, I
机构
[1] Univ Paris 05, INSERM, Fac Med Necker Enfants Malad, F-75730 Paris 15, France
[2] Hop Robert Debre, INSERM, U458, F-75935 Paris 19, France
[3] Museum Natl Hist Nat, Serv Systemat Mol, GDR CNRS 1005, F-75231 Paris 05, France
[4] INSERM, U155, F-94276 Le Kremlin Bicetre, France
[5] Genopole, ACTGene Rech & Dev, F-91035 Evry, France
[6] Columbia Univ Coll Phys & Surg, Dept Genet & Dev, New York, NY 10032 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1016/S0092-8674(00)00175-6
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Mutation and subsequent recombination events create genetic diversity, which is subjected to natural selection. Bacterial mismatch repair (MMR) deficient mutants, exhibiting high mutation and homeologous recombination rates, are frequently found in natural populations. Therefore, we have explored the possibility that MMR deficiency emerging in nature has left some "imprint" in the sequence of bacterial genomes. Comparative molecular phylogeny of MMR genes from natural Escherichia coli isolates shows that, compared to housekeeping genes, individual functional MMR genes exhibit high sequence mosaicism derived from diverse phylogenetic lineages. This apparent horizontal gene transfer correlates with hyperrecombination phenotype of MMR-deficient mutators. The sequence mosaicism of MMR genes may be a hallmark of a mechanism of adaptive evolution that involves modulation of mutation and recombination rates by recurrent losses and reacquisitions of MMR gene functions.
引用
收藏
页码:711 / 721
页数:11
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