Regulation of the HpyII restriction-modification system of Helicobacter pylori by gene deletion and horizontal reconstitution

被引:25
作者
Aras, RA [1 ]
Takata, T
Ando, T
van der Ende, A
Blaser, MJ
机构
[1] NYU, Sch Med, Dept Med, New York, NY 10003 USA
[2] NYU, Sch Med, Dept Microbiol, New York, NY USA
[3] Vet Adm Med Ctr, New York, NY 10010 USA
[4] Univ Amsterdam, Acad Med Ctr, Dept Med Microbiol, NL-1105 AZ Amsterdam, Netherlands
关键词
D O I
10.1046/j.1365-2958.2001.02637.x
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
Helicobacter pylori, Gram-negative, curved bacteria colonizing the human stomach, possess strain-specific complements of functional restriction-modification (R-M) systems. Restriction-modification systems have been identified in most bacterial species studied and are believed to have evolved to protect the host genome from invasion by foreign DNA. The large number of R-Ms homologous to those in other bacterial species and their strain-specificity suggest that H. pylori may have horizontally acquired these genes. A type IIs restriction-modification system, hpyIIRM, was active in two out of the six H. pylori strains studied. We demonstrate now that in most strains lacking M.HpyII function, there is compete absence of the R-M system. Direct DNA repeat of 80 bp flanking the hpyIIRM system allow its deletion, resulting in an 'empty-site' genotype. We show that strains possessing this empty-site genotype and strains with a full but inactive hpyIIRM can reacquire the hpyIIRM cassette and functional activity through natural transformation by DNA from the parental R-M+ strain. Identical isolates divergent for the presence of an active HpyII R-M pose different restriction barriers to transformation by foreign DNA. That H. pylori can lose HpyII R-M function through deletion or mutation, and can horizontally reacquire the hpyIIRM cassette, is, in composite, a novel mechanism for R-M regulation, supporting the general hypothesis that H. pylori populations use mutation and transformation to regulate gene function.
引用
收藏
页码:369 / 382
页数:14
相关论文
共 50 条
[1]   PCR-based subtractive hybridization and differences in gene content among strains of Helicobacter pylori [J].
Akopyants, NS ;
Fradkov, A ;
Diatchenko, L ;
Hill, JE ;
Siebert, PD ;
Lukyanov, SA ;
Sverdlov, ED ;
Berg, DE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (22) :13108-13113
[2]   Genomic-sequence comparison of two unrelated isolates of the human gastric pathogen Helicobacter pylori [J].
Alm, RA ;
Ling, LSL ;
Moir, DT ;
King, BL ;
Brown, ED ;
Doig, PC ;
Smith, DR ;
Noonan, B ;
Guild, BC ;
deJonge, BL ;
Carmel, G ;
Tummino, PJ ;
Caruso, A ;
Uria-Nickelsen, M ;
Mills, DM ;
Ives, C ;
Gibson, R ;
Merberg, D ;
Mills, SD ;
Jiang, Q ;
Taylor, DE ;
Vovis, GF ;
Trost, TJ .
NATURE, 1999, 397 (6715) :176-180
[3]   Restriction-modification system differences in Helicobacter pylori are a barrier to interstrain plasmid transfer [J].
Ando, T ;
Xu, Q ;
Torres, M ;
Kusugami, K ;
Israel, DA ;
Blaser, MJ .
MOLECULAR MICROBIOLOGY, 2000, 37 (05) :1052-1065
[4]   HP0333, a member of the dprA family, is involved in natural transformation in Helicobacter pylori [J].
Ando, T ;
Israel, DA ;
Kusugami, K ;
Blaser, MJ .
JOURNAL OF BACTERIOLOGY, 1999, 181 (18) :5572-5580
[5]   Cloning and characterization of the BglII restriction-modification system reveals a possible evolutionary footprint [J].
Anton, BP ;
Heiter, DF ;
Benner, JS ;
Hess, EJ ;
Greenough, L ;
Moran, LS ;
Slatko, BE ;
Brooks, JE .
GENE, 1997, 187 (01) :19-27
[6]   Clustering of meiotic double-strand breaks on yeast chromosome III [J].
Baudat, F ;
Nicolas, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (10) :5213-5218
[7]   Mechanisms of intron mobility [J].
Belfort, M ;
Perlman, PS .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (51) :30237-30240
[8]   Homing endonucleases: keeping the house in order [J].
Belfort, M ;
Roberts, RJ .
NUCLEIC ACIDS RESEARCH, 1997, 25 (17) :3379-3388
[9]   Helicobacter pylori genetic diversity and risk of human disease [J].
Blaser, MJ ;
Berg, DE .
JOURNAL OF CLINICAL INVESTIGATION, 2001, 107 (07) :767-773
[10]   CLONING AND CHARACTERIZATION OF THE MBOLL RESTRICTION-MODIFICATION SYSTEM [J].
BOCKLAGE, H ;
HEEGER, K ;
MULLERHILL, B .
NUCLEIC ACIDS RESEARCH, 1991, 19 (05) :1007-1013