Transposition of ISHp608, member of an unusual family of bacterial insertion sequences

被引:60
作者
Bao, TH
Guynet, C
Ronning, DR
Cointin-Marty, B
Dyda, F
Chandler, M
机构
[1] LMGM, CNRS, UMR5100, F-31062 Toulouse, France
[2] NIDDK, Mol Biol Lab, Bethesda, MD 20892 USA
关键词
excision; in vitro; in vivo; integration; transposase activity;
D O I
10.1038/sj.emboj.7600787
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
ISHp608 from Helicobacter pylori is active in Escherichia coli and represents a recently recognised group of insertion sequences. Its transposase and organisation suggest that it transposes using a different mechanism to that of other known transposons. The IS was shown to excise as a circular form, which is accompanied by the formation of a resealed donor plasmid backbone. We also demonstrate that TnpA, which is less than half the length of other transposases, is responsible for this and for ISHp608 transposition. Transposition was shown to be site specific: both insertion and transposon excision require a conserved target, 5'TTAC. Deletion analysis suggested that potential secondary structures at the left and right ends are important for transposition. In vitro TnpA bound both ends, showed a strong preference for a specific single-stranded DNA and introduced a single-strand break on the same strand at each end. Although many of the characteristics of ISHp608 appear similar to rolling-circle transposons, there are differences suggesting that, overall, transposition occurs by a different mechanism. The results have permitted the formulation of several related models.
引用
收藏
页码:3325 / 3338
页数:14
相关论文
共 36 条
[1]   Intramolecular transposition of insertion sequence IS91 results in second-site simple insertions [J].
Bernales, I ;
Mendiola, MV ;
de la Cruz, F .
MOLECULAR MICROBIOLOGY, 1999, 33 (02) :223-234
[2]   Conserved structure of IS200 elements in Salmonella [J].
Beuzon, CR ;
Casadesus, J .
NUCLEIC ACIDS RESEARCH, 1997, 25 (07) :1355-1361
[3]  
Beuzón CR, 2004, INT MICROBIOL, V7, P3
[4]   Repression of IS200 transposase synthesis by RNA secondary structures [J].
Beuzón, CR ;
Marqués, S ;
Casadesús, J .
NUCLEIC ACIDS RESEARCH, 1999, 27 (18) :3690-3695
[5]   LARGE-SCALE STABLE OPENING OF SUPERCOILED DNA IN RESPONSE TO TEMPERATURE AND SUPERCOILING IN (A + T)-RICH REGIONS THAT PROMOTE LOW-SALT CRUCIFORM EXTRUSION [J].
BOWATER, R ;
ABOULELA, F ;
LILLEY, DMJ .
BIOCHEMISTRY, 1991, 30 (49) :11495-11506
[6]   Nicking by transesterification: the reaction catalysed by a relaxase [J].
Byrd, DR ;
Matson, SW .
MOLECULAR MICROBIOLOGY, 1997, 25 (06) :1011-1022
[7]   IDENTIFICATION AND SEQUENCE OF GENE DICB - TRANSLATION OF THE DIVISION INHIBITOR FROM AN IN-PHASE INTERNAL START [J].
CAM, K ;
BEJAR, S ;
GIL, D ;
BOUCHE, JP .
NUCLEIC ACIDS RESEARCH, 1988, 16 (14) :6327-6338
[8]  
Chandler M., 2002, Mobile DNA II, P305, DOI DOI 10.1128/9781555817954.CH15
[9]  
Cornet F, 2004, MICROBIAL EVOLUTION: GENE ESTABLISHMENT, SURVIVAL, AND EXCHANGE, P36
[10]   MULTIPLE SEQUENCE ALIGNMENT WITH HIERARCHICAL-CLUSTERING [J].
CORPET, F .
NUCLEIC ACIDS RESEARCH, 1988, 16 (22) :10881-10890