CLONING AND LINKAGE ANALYSIS OF NEISSERIA-GONORRHOEAE DNA METHYLTRANSFERASES

被引:14
作者
GUNN, JS [1 ]
PIEKAROWICZ, A [1 ]
CHIEN, R [1 ]
STEIN, DC [1 ]
机构
[1] UNIV MARYLAND,DEPT MICROBIOL,COLL PK,MD 20742
关键词
D O I
10.1128/JB.174.17.5654-5660.1992
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
We have cloned DNA methyltransferases (MTases) from various strains of Neisseria gonorrhoeae. Each of these clones represents a single specificity, indicating that the multiple gonococcal MTase specificities are encoded by monospecific MTases. The DNAs of five strains (FA5100, F62, MS11, Pgh3-2, and WR302) were digested with NheI, SpeI, or NheI plus SpeI and subjected to pulsed-field gel electrophoresis. The DNA MTase clones were used to probe Southern blots of these pulsed-field gels to determine whether the MTase genes are linked and whether there are strain-to-strain differences. The results indicate that none of these genes are closely linked, but variable hybridization patterns indicate that there exist restriction fragment length polymorphisms between the strains tested. Most of the chromosomal regions containing these restriction fragment length polymorphisms are clustered in regions containing gonococcal genes known or suspected to antigenically vary via genetic recombination.
引用
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页码:5654 / 5660
页数:7
相关论文
共 25 条
[1]   PHYSICAL AND GENETIC-MAP OF THE NEISSERIA-GONORRHOEAE STRAIN MS11-N198 CHROMOSOME [J].
BIHLMAIER, A ;
ROMLING, U ;
MEYER, TF ;
TUMMLER, B ;
GIBBS, CP .
MOLECULAR MICROBIOLOGY, 1991, 5 (10) :2529-2539
[2]   CONSTRUCTION AND CHARACTERIZATION OF NEW CLONING VEHICLES .2. MULTIPURPOSE CLONING SYSTEM [J].
BOLIVAR, F ;
RODRIGUEZ, RL ;
GREENE, PJ ;
BETLACH, MC ;
HEYNEKER, HL ;
BOYER, HW ;
CROSA, JH ;
FALKOW, S .
GENE, 1977, 2 (02) :95-113
[3]  
CHIEN RH, 1991, THESIS U MARYLAND
[4]   RECOMBINATION AMONG PROTEIN-II GENES OF NEISSERIA-GONORRHOEAE GENERATES NEW CODING SEQUENCES AND INCREASES STRUCTURAL VARIABILITY IN THE PROTEIN-II FAMILY [J].
CONNELL, TD ;
BLACK, WJ ;
KAWULA, TH ;
BARRITT, DS ;
DEMPSEY, JA ;
KVERNELAND, K ;
STEPHENSON, A ;
SCHEPART, BS ;
MURPHY, GL ;
CANNON, JG .
MOLECULAR MICROBIOLOGY, 1988, 2 (02) :227-236
[5]   PHYSICAL MAP OF THE CHROMOSOME OF NEISSERIA-GONORRHOEAE FA1090 WITH LOCATIONS OF GENETIC-MARKERS, INCLUDING OPA AND PIL GENES [J].
DEMPSEY, JAF ;
LITAKER, W ;
MADHURE, A ;
SNODGRASS, TL ;
CANNON, JG .
JOURNAL OF BACTERIOLOGY, 1991, 173 (17) :5476-5486
[6]  
DRAZEK S, 1992, THESIS U MARYLAND
[7]   MULTISPECIFIC DNA METHYLTRANSFERASES FROM BACILLUS-SUBTILIS PHAGES - PROPERTIES OF WILD-TYPE AND VARIOUS MUTANT ENZYMES WITH ALTERED DNA AFFINITY [J].
GUNTHERT, U ;
LAUSTER, R ;
REINERS, L .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1986, 159 (03) :485-492
[8]   RELEASE OF SOLUBLE PILIN ANTIGEN COUPLED WITH GENE CONVERSION IN NEISSERIA-GONORRHOEAE [J].
HAAS, R ;
SCHWARZ, H ;
MEYER, TF .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (24) :9079-9083
[9]   INTRAGENIC RECOMBINATION LEADS TO PILUS ANTIGENIC VARIATION IN NEISSERIA-GONORRHOEAE [J].
HAGBLOM, P ;
SEGAL, E ;
BILLYARD, E ;
SO, M .
NATURE, 1985, 315 (6015) :156-158
[10]   NEISSERIA GONORRHOEAE .1. VIRULENCE GENETICALLY LINKED TO CLONAL VARIATION [J].
KELLOGG, DS ;
PEACOCK, WL ;
PIRKLE, CI ;
DEACON, WE ;
BROWN, L .
JOURNAL OF BACTERIOLOGY, 1963, 85 (06) :1274-&