The Streptomyces genome contains multiple pseudo-attB sites for the φC31-encoded site-specific recombination system

被引:113
作者
Combes, P [1 ]
Till, R [1 ]
Bee, S [1 ]
Smith, MCM [1 ]
机构
[1] Univ Nottingham, Queens Med Ctr, Genet Inst, Nottingham NG7 2UH, England
关键词
D O I
10.1128/JB.184.20.5746-5752.2002
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The integrase from the Streptomyces phage phiC31 is a member of the serine recombinase family of site-specific recombinases and is fundamentally different from that of lambda or its relatives. Moreover, phiC31 int/attP is used widely as an essential component of integration vectors (such as pSET152) employed in the genetic analysis of Streptomyces species. phiC31 or integrating plasmids containing int/attP have been shown previously to integrate at a locus, attB, in the chromosome. The DNA sequences of the attB sites of various Streptomyces species revealed nonconserved positions. In particular, the crossover site was narrowed to the sequence 57T present in both attP and attB. Strains of Streptomyces coelicolor and S. lividans were constructed with a deletion of the attB site (DeltaattB), and pSET152 was introduced into these strains by conjugation. Thus, secondary or pseudo-attB sites were identified by Southern blotting and after rescue of plasmids containing DNA flanking the insertion sites from the chromosome. The sequences of the integration sites had similarity to those of attB. Analysis of the insertions of pSET152 into both attB(+) and DeltaattB strains indicated that this plasmid can integrate at several loci via independent recombination events within a transconjugant.
引用
收藏
页码:5746 / 5752
页数:7
相关论文
共 25 条
[1]   2 GENES INVOLVED IN THE PHASE-VARIABLE PHI-C31 RESISTANCE MECHANISM OF STREPTOMYCES-COELICOLOR A3(2) [J].
BEDFORD, DJ ;
LAITY, C ;
BUTTNER, MJ .
JOURNAL OF BACTERIOLOGY, 1995, 177 (16) :4681-4689
[2]   Complete genome sequence of the model actinomycete Streptomyces coelicolor A3(2) [J].
Bentley, SD ;
Chater, KF ;
Cerdeño-Tárraga, AM ;
Challis, GL ;
Thomson, NR ;
James, KD ;
Harris, DE ;
Quail, MA ;
Kieser, H ;
Harper, D ;
Bateman, A ;
Brown, S ;
Chandra, G ;
Chen, CW ;
Collins, M ;
Cronin, A ;
Fraser, A ;
Goble, A ;
Hidalgo, J ;
Hornsby, T ;
Howarth, S ;
Huang, CH ;
Kieser, T ;
Larke, L ;
Murphy, L ;
Oliver, K ;
O'Neil, S ;
Rabbinowitsch, E ;
Rajandream, MA ;
Rutherford, K ;
Rutter, S ;
Seeger, K ;
Saunders, D ;
Sharp, S ;
Squares, R ;
Squares, S ;
Taylor, K ;
Warren, T ;
Wietzorrek, A ;
Woodward, J ;
Barrell, BG ;
Parkhill, J ;
Hopwood, DA .
NATURE, 2002, 417 (6885) :141-147
[3]   PLASMID CLONING VECTORS FOR THE CONJUGAL TRANSFER OF DNA FROM ESCHERICHIA-COLI TO STREPTOMYCES SPP [J].
BIERMAN, M ;
LOGAN, R ;
OBRIEN, K ;
SENO, ET ;
RAO, RN ;
SCHONER, BE .
GENE, 1992, 116 (01) :43-49
[4]  
Breüner A, 1999, J BACTERIOL, V181, P7291
[5]   LAMBDOID PHAGES AS ELEMENTS OF BACTERIAL GENOMES (INTEGRASE PHAGE21 ESCHERICHIA-COLI K-12 ICD GENE) [J].
CAMPBELL, A ;
SCHNEIDER, SJ ;
SONG, B .
GENETICA, 1992, 86 (1-3) :259-267
[6]   Taking a genetic scalpel to the Streptomyces colony [J].
Chater, KF .
MICROBIOLOGY-UK, 1998, 144 :1465-1478
[7]  
GRINDLEY NDF, 1994, NUCLEIC ACIDS MOL BI, V8, P236
[8]   A phage integrase directs efficient site-specific integration in human cells [J].
Groth, AC ;
Olivares, EC ;
Thyagarajan, B ;
Calos, MP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (11) :5995-6000
[9]  
Hatfull GF, 1988, GENETIC RECOMBINATIO, P357
[10]   Forty years of genetics with Streptomyces:: from in vivo through in vitro to in silico [J].
Hopwood, DA .
MICROBIOLOGY-UK, 1999, 145 :2183-2202