Analysis and characterization of the IncFV plasmid pED208 transfer region

被引:35
作者
Jun, L
Manchak, J
Klimke, W
Davidson, C
Firth, N
Skurray, RA
Frost, LS
机构
[1] Univ Alberta, Dept Biol Sci, Edmonton, AB T6G 2E9, Canada
[2] Univ Sydney, Sch Biol Sci, Sydney, NSW 2006, Australia
基金
加拿大健康研究院; 澳大利亚研究理事会;
关键词
pED208; F(0)lac transfer region; DNA sequence; conjugation; regulation; specificity; coupling protein; relaxase; type IV secretion;
D O I
10.1016/S0147-619X(02)00007-0
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
pED208 is a transfer-derepressed mutant of the IncFV plasmid, F(0)lac, which has an IS2 element inserted in its traY gene, resulting in constitutive overexpression of its transfer (tra) region. The pED208 transfer region, which encodes proteins responsible for pilus synthesis and conjugative plasmid transfer, was sequenced and found to be very similar to the F tra region in terms of its organization although most pED208 tra proteins share only about 45% amino acid identity. All the essential genes for F transfer had homologs within the pED208 transfer region with the exception of traQ, which encodes the chaperone for stable F-pilin expression. F(0)lac appears to have a fertility inhibition system different than the FinOP system of other F-like plasmids, and its transfer efficiency was increased in the presence of F or R 100, suggesting that it could be mobilized by these plasmids, The F-like transfer systems specified by F, R100, and F(0)lac were highly specific for their cognate origins of transfer (oriT) as measured by their abilities to mobilize chimeric oriT-containing plasmids. (C) 2002 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:24 / 37
页数:14
相关论文
共 78 条
[1]   Comparison of proteins involved in pilus synthesis and mating pair stabilization from the related plasmids F and R100-1: Insights into the mechanism of conjugation [J].
Anthony, KG ;
Klimke, WA ;
Manchak, J ;
Frost, LS .
JOURNAL OF BACTERIOLOGY, 1999, 181 (17) :5149-5159
[2]   ESSENTIAL MOTIFS OF RELAXASE (TRAI) AND TRAG PROTEINS INVOLVED IN CONJUGATIVE TRANSFER OF PLASMID-RP4 [J].
BALZER, D ;
PANSEGRAU, W ;
LANKA, E .
JOURNAL OF BACTERIOLOGY, 1994, 176 (14) :4285-4295
[3]   COMPARISON OF DEOXYRIBONUCLEIC-ACID MOLECULAR-WEIGHTS AND HOMOLOGIES OF PLASMIDS CONFERRING LINKED RESISTANCE TO STREPTOMYCIN AND SULFONAMIDES [J].
BARTH, PT ;
GRINTER, NJ .
JOURNAL OF BACTERIOLOGY, 1974, 120 (02) :618-630
[4]  
Bradley D. E., 1981, MOL BIOL PATHOGENICI, P217
[5]   SEROLOGICAL CHARACTERISTICS OF PILI DETERMINED BY PLASMIDS-R711B AND F0LAC [J].
BRADLEY, DE ;
MEYNELL, E .
JOURNAL OF GENERAL MICROBIOLOGY, 1978, 108 (SEP) :141-149
[6]   NUCLEOTIDE-SEQUENCE OF THE TRAI (HELICASE-I) GENE FROM THE SEX FACTOR-F [J].
BRADSHAW, HD ;
TRAXLER, BA ;
MINKLEY, EG ;
NESTER, EW ;
GORDON, MP .
JOURNAL OF BACTERIOLOGY, 1990, 172 (07) :4127-4131
[7]   Nicking by transesterification: the reaction catalysed by a relaxase [J].
Byrd, DR ;
Matson, SW .
MOLECULAR MICROBIOLOGY, 1997, 25 (06) :1011-1022
[8]   Genetic evidence of a coupling role for the TraG protein family in bacterial conjugation [J].
Cabezon, E ;
Sastre, JI ;
delaCruz, F .
MOLECULAR & GENERAL GENETICS, 1997, 254 (04) :400-406
[9]   COINTEGRATE FORMATION MEDIATED BY TN9 .2. ACTIVITY OF IS1 IS MODULATED BY EXTERNAL DNA-SEQUENCES [J].
CHANDLER, M ;
GALAS, DJ .
JOURNAL OF MOLECULAR BIOLOGY, 1983, 170 (01) :61-91
[10]  
CHEAH KC, 1968, J GEN MICROBIOL, V123, P3269