Evidence for recombination in the microcystin synthetase (mcy) genes of toxic cyanobacteria Microcystiis spp.

被引:78
作者
Tanabe, Y [1 ]
Kaya, K [1 ]
Watanabe, MM [1 ]
机构
[1] Natl Inst Environm Studies, Div Environm Biol, Tsukuba, Ibaraki 3058506, Japan
关键词
cyanobacteria; microcystin synthetase; Microcystis; NRPS; recombination; split decomposition;
D O I
10.1007/s00239-004-2583-1
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
Recombination has been suggested to be an important factor for the genetic variation of bacterial genes, but few Studies have dealt with intragenic recombination between the same or closely related species of cyanobacteria. Here we provide strong evidence for recombination in the nucrocystin synthetase (mcy) gene Cluster of the toxic cyanobacteria pp. This gene cluster contains 10 genes Microcystis spp. (mcyA to J) that encode a mixed polyketide synthase (PKS)/nonribosomal peptide synthetase (NRPS) complex. mcy gene sequences were determined for four selected regions (within mcyA, D, G, and J) within the mcy gene cluster from 1 Canadian and 10 Asian toxic Microcystis and compared with previously published mcy sequences. Split decomposition analysis indicated a reticulate phylogeny of mcyA, and several potential recombination tracts or mcyA were identified by the RDP analysis and a runs test implemented in GENECONV. In contrast, no recombination was detected in the mcyD, G, and J sequences. However, discrepancies among the four mcy gene genealogies were evident from the results Of independent split decomposition analyses,. which were Further supported by incongruence length difference (ILD) tests. Taken together, these findings suggest that both intragenic and intergenic recombination within the mcy gene cluster contributes to the genetic diversity of the mcy genes of Microcystis spp.
引用
收藏
页码:633 / 641
页数:9
相关论文
共 44 条
[1]  
[Anonymous], 1999, GENECONV: A computer package for the statistical detection of gene conversion
[2]   Biochemistry - Harnessing the biosynthetic code: Combinations, permutations, and mutations [J].
Cane, DE ;
Walsh, CT ;
Khosla, C .
SCIENCE, 1998, 282 (5386) :63-68
[3]   Insertional mutagenesis of a peptide synthetase gene that is responsible for hepatotoxin production in the cyanobacterium Microcystis aeruginosa PCC 7806 [J].
Dittmann, E ;
Neilan, BA ;
Erhard, M ;
vonDohren, H ;
Borner, T .
MOLECULAR MICROBIOLOGY, 1997, 26 (04) :779-787
[4]   Parsimony jackknifing outperforms neighbor-joining [J].
Farris, JS ;
Albert, VA ;
Kallersjo, M ;
Lipscomb, D ;
Kluge, AG .
CLADISTICS, 1996, 12 (02) :99-124
[5]   A comparison of the nucleotide sequences of the adk and recA genes of pathogenic and commensal Neisseria species: Evidence for extensive interspecies recombination within adk [J].
Feil, E ;
Zhou, JJ ;
Smith, JM ;
Spratt, BG .
JOURNAL OF MOLECULAR EVOLUTION, 1996, 43 (06) :631-640
[6]  
GOLDMAN N, 1994, MOL BIOL EVOL, V11, P725
[7]   SplitsTree: analyzing and visualizing evolutionary data [J].
Huson, DH .
BIOINFORMATICS, 1998, 14 (01) :68-73
[8]  
Janson S, 2002, INT J SYST EVOL MICR, V52, P1397, DOI [10.1099/ijs.0.02111-0, 10.1099/00207713-52-4-1397]
[9]   Diversity of microcystin genes within a population of the toxic cyanobacterium Microcystis spp. in Lake Wannsee (Berlin, Germany) [J].
Kurmayer, R ;
Dittmann, E ;
Fastner, J ;
Chorus, I .
MICROBIAL ECOLOGY, 2002, 43 (01) :107-118
[10]   RECOMBINATIONAL BASIS OF SEROVAR DIVERSITY IN SALMONELLA-ENTERICA [J].
LI, J ;
NELSON, K ;
MCWHORTER, AC ;
WHITTAM, TS ;
SELANDER, RK .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (07) :2552-2556