Control of directionality in integrase-mediated recombination: examination of recombination directionality factors (RDFs) including Xis and Cox proteins

被引:148
作者
Lewis, JA
Hatfull, GF [1 ]
机构
[1] Univ Pittsburgh, Pittsburgh Bacteriol Inst, Pittsburgh, PA 15260 USA
[2] Univ Pittsburgh, Dept Sci Biol, Pittsburgh, PA 15260 USA
关键词
D O I
10.1093/nar/29.11.2205
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
Similarity between the DNA substrates and products of integrase-mediated site-specific recombination reactions results in a single recombinase enzyme being able to catalyze both the integration and excision reactions. The control of directionality in these reactions is achieved through a class of small accessory factors that favor one reaction while interfering with the other. These proteins, which we will refer to collectively as recombination directionality factors (RDFs), play architectural roles in reactions catalyzed by their cognate recombinases and have been identified in conjunction with both tyrosine and serine integrases, Previously identified RDFs are typically small, basic and have diverse amino acid sequences, A subset of RDFs, the cox genes, also function as transcriptional regulators. We present here a compilation of all the known RDF proteins as well as those identified through database mining that we predict to be involved in conferring recombination directionality, Analysis of this group of proteins shows that they can be grouped into distinct subgroups based on their sequence similarities and that they are likely to have arisen from several independent evolutionary lineages. This compilation will prove useful in recognizing new proteins that confer directionality upon site-specific recombination reactions encoded by plasmids, transposons, phages and prophages.
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收藏
页码:2205 / 2216
页数:12
相关论文
共 83 条
[1]  
ABREMSKI K, 1982, J BIOL CHEM, V257, P9658
[2]   Gapped BLAST and PSI-BLAST: a new generation of protein database search programs [J].
Altschul, SF ;
Madden, TL ;
Schaffer, AA ;
Zhang, JH ;
Zhang, Z ;
Miller, W ;
Lipman, DJ .
NUCLEIC ACIDS RESEARCH, 1997, 25 (17) :3389-3402
[3]  
ALTSCHUL SF, 1990, J MOL BIOL, V215, P403, DOI 10.1006/jmbi.1990.9999
[4]  
BAKER J, 1991, NEW BIOL, V3, P297
[5]   EFFICIENT EXCISION OF PHAGE LAMBDA FROM THE ESCHERICHIA-COLI CHROMOSOME REQUIRES THE FIS PROTEIN [J].
BALL, CA ;
JOHNSON, RC .
JOURNAL OF BACTERIOLOGY, 1991, 173 (13) :4027-4031
[6]   The complete genome sequence of Escherichia coli K-12 [J].
Blattner, FR ;
Plunkett, G ;
Bloch, CA ;
Perna, NT ;
Burland, V ;
Riley, M ;
ColladoVides, J ;
Glasner, JD ;
Rode, CK ;
Mayhew, GF ;
Gregor, J ;
Davis, NW ;
Kirkpatrick, HA ;
Goeden, MA ;
Rose, DJ ;
Mau, B ;
Shao, Y .
SCIENCE, 1997, 277 (5331) :1453-+
[7]   THE INTEGRATED CONJUGATIVE PLASMID PSAM2 OF STREPTOMYCES-AMBOFACIENS IS RELATED TO TEMPERATE BACTERIOPHAGES [J].
BOCCARD, F ;
SMOKVINA, T ;
PERNODET, JL ;
FRIEDMANN, A ;
GUERINEAU, M .
EMBO JOURNAL, 1989, 8 (03) :973-980
[8]   Partial characterization of a genomic island associated with the multidrug resistance region of Salmonella enterica Typhymurium DT104 [J].
Boyd, DA ;
Peters, GA ;
Ng, LK ;
Mulvey, MR .
FEMS MICROBIOLOGY LETTERS, 2000, 189 (02) :285-291
[9]   EXCISIVE RECOMBINATION OF THE SLP1 ELEMENT IN STREPTOMYCES-LIVIDANS IS MEDIATED BY INT AND ENHANCED BY XIS [J].
BRASCH, MA ;
COHEN, SN .
JOURNAL OF BACTERIOLOGY, 1993, 175 (10) :3075-3082
[10]  
Breüner A, 1999, J BACTERIOL, V181, P7291