Determinants of segregational stability of the linear plasmid-prophage N15 of Escherichia coli

被引:34
作者
Grigoriev, PS
Lobocka, MB [1 ]
机构
[1] Polish Acad Sci, Inst Biochem & Biophys, Dept Microbial Biochem, PL-02106 Warsaw, Poland
[2] State Tech Univ, Dept Biophys, St Petersburg 19251, Russia
关键词
D O I
10.1046/j.1365-2958.2001.02632.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
N15 is a bacteriophage of Escherichia coli that resembles lambda, but, unlike lambda, it lysogenizes as a linear plasmid. We show that stable maintenance of this unusual plasmid-prophage depends on the parA and parB genes, relatives of the partition genes of F and P1 plasmids. ParB of N15, like its F- and Pl-encoded homologues, destabilizes plasmids carrying its target centromere, when present in excess. Within the genome of N15, we identified four unlinked, palindromic sequences that can promote the ParB-mediated destabilization of a moderate-copy vector in cis. They are distant from the parAB operon, unlike the centromeric sites of F and P1. Each of these palindromes could interact in vivo and in vitro with ParB. Each, when cloned separately, had properties characteristic of centromeric sites: exerted incompatibility against the N15 prophage and mini-N15 plasmids, and stabilized a mini-P1 plasmid depleted of its own partition genes when ParA and ParB of N15 were supplied. A pair of sites was more effective than a single site. Two of the centromeric sites are located in the proximity of promoters of phage genes, suggesting that, in addition to their function in partitioning of N15 prophage, they may control expression of N15 lytic functions.
引用
收藏
页码:355 / 368
页数:14
相关论文
共 52 条
[1]   PARTITION OF UNIT-COPY MINIPLASMIDS TO DAUGHTER CELLS .3. THE DNA-SEQUENCE AND FUNCTIONAL-ORGANIZATION OF THE P1-PARTITION REGION [J].
ABELES, AL ;
FRIEDMAN, SA ;
AUSTIN, SJ .
JOURNAL OF MOLECULAR BIOLOGY, 1985, 185 (02) :261-272
[2]   PARTITION-MEDIATED INCOMPATIBILITY OF BACTERIAL PLASMIDS [J].
AUSTIN, S ;
NORDSTROM, K .
CELL, 1990, 60 (03) :351-354
[3]   PARTITION-FUNCTIONS OF MINI-F AFFECT PLASMID DNA TOPOLOGY IN ESCHERICHIA-COLI [J].
BIEK, DP ;
STRINGS, J .
JOURNAL OF MOLECULAR BIOLOGY, 1995, 246 (03) :388-400
[4]   A COMPUTER ALGORITHM FOR TESTING POTENTIAL PROKARYOTIC TERMINATORS [J].
BRENDEL, V ;
TRIFONOV, EN .
NUCLEIC ACIDS RESEARCH, 1984, 12 (10) :4411-4427
[5]   A PSC101-DERIVED PLASMID WHICH SHOWS NO SEQUENCE HOMOLOGY TO OTHER COMMONLY USED CLONING VECTORS [J].
CHURCHWARD, G ;
BELIN, D ;
NAGAMINE, Y .
GENE, 1984, 31 (1-3) :165-171
[6]   BIOCHEMICAL ACTIVITIES OF THE PARA PARTITION PROTEIN OF THE P1 PLASMID [J].
DAVIS, MA ;
MARTIN, KA ;
AUSTIN, SJ .
MOLECULAR MICROBIOLOGY, 1992, 6 (09) :1141-1147
[7]   The protelomerase of temperate Escherichia coli phage N15 has cleaving-joining activity [J].
Deneke, J ;
Ziegelin, G ;
Lurz, R ;
Lanka, E .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (14) :7721-7726
[8]  
ELISH ME, 1988, J GEN MICROBIOL, V134, P1355
[9]   Intracellular localization of P1 ParB protein depends on ParA and parS [J].
Erdmann, N ;
Petroff, T ;
Funnell, BE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (26) :14905-14910