Transposon-mediated site-specific recombination in vitro: DNA cleavage and protein-DNA linkage at the recombination site

Cell ◽  
1981 ◽  
Vol 25 (3) ◽  
pp. 721-728 ◽  
Author(s):  
R.R. Reed ◽  
N.D.F. Grindley
Author(s):  
Julie F. Senecoff ◽  
Robert C. Bruckner ◽  
Leslie Meyer-Leon ◽  
Cynthia A. Gates ◽  
Elizabeth Wood ◽  
...  

2019 ◽  
Vol 201 (24) ◽  
Author(s):  
Ali Farrokhi ◽  
Hua Liu ◽  
George Szatmari

ABSTRACT Chromosome dimers occur in bacterial cells as a result of the recombinational repair of DNA. In most bacteria, chromosome dimers are resolved by XerCD site-specific recombination at the dif (deletion-induced filamentation) site located in the terminus region of the chromosome. Caulobacter crescentus, a Gram-negative oligotrophic bacterium, also possesses Xer recombinases, called CcXerC and CcXerD, which have been shown to interact with the Escherichia coli dif site in vitro. Previous studies on Caulobacter have suggested the presence of a dif site (referred to in this paper as dif1CC), but no in vitro data have shown any association with this site and the CcXer proteins. Using recursive hidden Markov modeling, another group has proposed a second dif site, which we call dif2CC, which shows more similarity to the dif consensus sequence. Here, by using a combination of in vitro experiments, we compare the affinities and the cleavage abilities of CcXerCD recombinases for both dif sites. Our results show that dif2CC displays a higher affinity for CcXerC and CcXerD and is bound cooperatively by these proteins, which is not the case for the original dif1CC site. Furthermore, dif2CC nicked substrates are more efficiently cleaved by CcXerCD, and deletion of the site results in about 5 to 10% of cells showing an altered cellular morphology. IMPORTANCE Bacteria utilize site-specific recombination for a variety of purposes, including the control of gene expression, acquisition of genetic elements, and the resolution of dimeric chromosomes. Failure to resolve dimeric chromosomes can lead to cell division defects in a percentage of the cell population. The work presented here shows the existence of a chromosomal resolution system in C. crescentus. Defects in this resolution system result in the formation of chains of cells. Further understanding of how these cells remain linked together will help in the understanding of how chromosome segregation and cell division are linked in C. crescentus.


1996 ◽  
Vol 15 (5) ◽  
pp. 1172-1181 ◽  
Author(s):  
S. D. Colloms ◽  
R. McCulloch ◽  
K. Grant ◽  
L. Neilson ◽  
D. J. Sherratt

1984 ◽  
Vol 3 (10) ◽  
pp. 2415-2421 ◽  
Author(s):  
Gabriele Mertens ◽  
Andrea Hoffmann ◽  
Helmut Blöcker ◽  
Ronald Frank ◽  
Regine Kahmann

2009 ◽  
Vol 192 (3) ◽  
pp. 883-887 ◽  
Author(s):  
Tung Tran ◽  
David J. Sherratt ◽  
Marcelo E. Tolmasky

ABSTRACT Salmonella plasmid pFPTB1 includes a Tn3-like transposon and a Xer recombination site, fpr, which mediates site-specific recombination at efficiencies lower than those required for stabilizing a plasmid by dimer resolution. Mutagenesis and comparative studies with mwr, a site closely related to fpr, indicate that there is an interdependence of the sequences in the XerC binding region and the central region in Xer site-specific recombination sites.


1983 ◽  
Vol 80 (23) ◽  
pp. 7284-7288 ◽  
Author(s):  
D. Vetter ◽  
B. J. Andrews ◽  
L. Roberts-Beatty ◽  
P. D. Sadowski

2003 ◽  
Vol 185 (10) ◽  
pp. 3076-3080 ◽  
Author(s):  
Dominic Esposito ◽  
Gary F. Gerard

ABSTRACT The Escherichia coli nucleoid-associated protein Fis was previously shown to be involved in bacteriophage lambda site-specific recombination in vivo, enhancing the levels of both integrative recombination and excisive recombination. While purified Fis protein was shown to stimulate in vitro excision, Fis appeared to have no effect on in vitro integration reactions even though a 15-fold drop in lysogenization frequency had previously been observed in fis mutants. We demonstrate here that E. coli Fis protein does stimulate integrative lambda recombination in vitro but only under specific conditions which likely mimic natural in vivo recombination more closely than the standard conditions used in vitro. In the presence of suboptimal concentrations of Int protein, Fis stimulates the rate of integrative recombination significantly. In addition, Fis enhances the recombination of substrates with nonstandard topologies which may be more relevant to the process of in vivo phage lambda recombination. These data support the hypothesis that Fis may play an essential role in lambda recombination in the host cell.


2008 ◽  
Vol 190 (19) ◽  
pp. 6392-6397 ◽  
Author(s):  
Lin Zhang ◽  
Xijun Ou ◽  
Guoping Zhao ◽  
Xiaoming Ding

ABSTRACT The Streptomyces phage φBT1 encodes a site-specific integrase of the large serine recombinase subfamily. In this report, the enzymatic activity of the φBT1 integrase was characterized in vitro. We showed that this integrase has efficient integration activity with substrate DNAs containing attB and attP sites, independent of DNA supercoiling or cofactors. Both intra- and intermolecular recombinations proceed with rapid kinetics. The recombination is highly specific, and no reactions are observed between pairs of sites including attB and attL, attB and attR, attP and attL, or attP and attR or between two identical att sequences; however, a low but significant frequency of excision recombination between attL and attR is observed in the presence of the φBT1 integrase alone. In addition, for efficient integration, the minimal sizes of attB and attP are 36 bp and 48 bp, respectively. This site-specific recombination system is efficient and simple to use; thus, it could have applications for the manipulation of DNA in vitro.


1984 ◽  
Vol 49 (0) ◽  
pp. 751-760 ◽  
Author(s):  
R.C. Johnson ◽  
M.B. Bruist ◽  
M.B. Glaccum ◽  
M.I. Simon

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