Mutational analysis of the R64 oriT region: Requirement for precise location of the NikA binding sequence

被引:17
作者
Furuya, N [1 ]
Komano, T [1 ]
机构
[1] TOKYO METROPOLITAN UNIV,DEPT BIOL,HACHIOJI,TOKYO 19203,JAPAN
关键词
D O I
10.1128/jb.179.23.7291-7297.1997
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Conjugative DNA transfer of IncI1 plasmid R64 is initiated by the introduction of a site- and strand-specific nick into the origin of transfer (oriT). In R64 oriT, 17-bp (repeat A and B) and 8-bp inverted-repeat sequences with mismatches are located 8 bp away from the nick site. The nicking is mediated by R64 NikA and NikB proteins. To analyze the functional organization of the R64 oriT region, various deletion, insertion, and substitution mutations were introduced into a 92-bp minimal R64 oriT sequence and their effects on oriT function were investigated. This detailed analysis confirms our previous prediction that the R64 oriT region consists of an oriT core sequence and additional sequences necessary for full oriT activity. The oriT core sequence consists of the repeat A sequence, which is recognized by R64 NikA protein, and the nick region sequence, which is conserved among various origins of transfer and is most probably recognized by NikB protein. The oriT core sequence is sufficient for NikAB-mediated oriT-specific nicking. Furthermore, it was shown that the repeat A sequence is essential for localization to a precise position relative to the nick site for oriT function. This seems to be required for the formation of a functional ternary complex consisting of NikA and NikB proteins and oriT DNA. The repeat B sequence and 8-bp inverted repeat sequences are suggested to be required for the termination of DNA transfer.
引用
收藏
页码:7291 / 7297
页数:7
相关论文
共 36 条
[21]   RELAXASE (TRAI) OF INCP-ALPHA PLASMID RP4 CATALYZES A SITE-SPECIFIC CLEAVING-JOINING REACTION OF SINGLE-STRANDED-DNA [J].
PANSEGRAU, W ;
SCHRODER, W ;
LANKA, E .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (07) :2925-2929
[22]   INVITRO ASSEMBLY OF RELAXOSOMES AT THE TRANSFER ORIGIN OF PLASMID-RP4 [J].
PANSEGRAU, W ;
BALZER, D ;
KRUFT, V ;
LURZ, R ;
LANKA, E .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (17) :6555-6559
[23]   COMMON SEQUENCE MOTIFS IN DNA RELAXASES AND NICK REGIONS FROM A VARIETY OF DNA TRANSFER SYSTEMS [J].
PANSEGRAU, W ;
LANKA, E .
NUCLEIC ACIDS RESEARCH, 1991, 19 (12) :3455-3455
[24]   ENDONUCLEASE ACTIVITY OF ESCHERICHIA-COLI DNA HELICASE-I DIRECTED AGAINST THE TRANSFER ORIGIN OF THE F-FACTOR [J].
REYGERS, U ;
WESSEL, R ;
MULLER, H ;
HOFFMANNBERLING, H .
EMBO JOURNAL, 1991, 10 (09) :2689-2694
[25]   SEQUENCE-ANALYSIS AND CHARACTERIZATION OF THE MOBILIZATION REGION OF A BROAD-HOST-RANGE PLASMID, PTF-FC2, ISOLATED FROM THIOBACILLUS-FERROOXIDANS [J].
ROHRER, J ;
RAWLINGS, DE .
JOURNAL OF BACTERIOLOGY, 1992, 174 (19) :6230-6237
[26]  
Sambrook J., 2002, MOL CLONING LAB MANU
[27]   INVITRO CLEAVAGE OF DOUBLE-STRANDED AND SINGLE-STRANDED-DNA BY PLASMID RSF1010-ENCODED MOBILIZATION PROTEINS [J].
SCHERZINGER, E ;
LURZ, R ;
OTTO, S ;
DOBRINSKI, B .
NUCLEIC ACIDS RESEARCH, 1992, 20 (01) :41-48
[28]   HIGH-COPY-NUMBER AND LOW-COPY-NUMBER PLASMID VECTORS FOR LACZ-ALPHA-COMPLEMENTATION AND CHLORAMPHENICOL-RESISTANCE OR KANAMYCIN-RESISTANCE SELECTION [J].
TAKESHITA, S ;
SATO, M ;
TOBA, M ;
MASAHASHI, W ;
HASHIMOTOGOTOH, T .
GENE, 1987, 61 (01) :63-74
[29]   INTRINSIC BENDS AND INTEGRATION HOST FACTOR BINDING AT F-PLASMID ORIT [J].
TSAI, MM ;
FU, YHF ;
DEONIER, RC .
JOURNAL OF BACTERIOLOGY, 1990, 172 (08) :4603-4609
[30]   PROCESSES AT THE NICK REGION LINK CONJUGATION, T-DNA TRANSFER AND ROLLING CIRCLE REPLICATION [J].
WATERS, VL ;
GUINEY, DG .
MOLECULAR MICROBIOLOGY, 1993, 9 (06) :1123-1130