Literature DB >> 10852483

Core-binding specificity of bacteriophage integrases.

P Gottfried1, E Yagil, M Kolot.   

Abstract

The site-specific recombination systems of bacteriophages lambda and HK022 share the same mechanism and their integrase proteins show strong homology. Nevertheless the integrase protein of each phage can only catalyze recombination between its own att sites. Previous work has shown that the specificity determinants in the att sites are located within the sequences that bind the integrase to the core of att. DNA fragments that carry attL and attR sites of each phage were challenged with each of the two integrases and the DNA-protein complexes were examined by the gel-retardation technique. The results show that each integrase can form higher-order DNA-protein complexes only with its cognate att sites, suggesting that differences in the mode of binding to the core are responsible for the specificity difference between the two integrases.

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Year:  2000        PMID: 10852483     DOI: 10.1007/s004380051209

Source DB:  PubMed          Journal:  Mol Gen Genet        ISSN: 0026-8925


  3 in total

1.  Arm site independence of coliphage HK022 integrase in human cells.

Authors:  Natalia Malchin; Chen N Tuby; Ezra Yagil; Mikhail Kolot
Journal:  Mol Genet Genomics       Date:  2011-03-26       Impact factor: 3.291

2.  Transfer of the symbiotic plasmid of Rhizobium etli CFN42 requires cointegration with p42a, which may be mediated by site-specific recombination.

Authors:  Susana Brom; Lourdes Girard; Cristina Tun-Garrido; Alejandro García-de los Santos; Patricia Bustos; Víctor González; David Romero
Journal:  J Bacteriol       Date:  2004-11       Impact factor: 3.490

3.  Unmasking the ancestral activity of integron integrases reveals a smooth evolutionary transition during functional innovation.

Authors:  Jose Antonio Escudero; Celine Loot; Vincent Parissi; Aleksandra Nivina; Christiane Bouchier; Didier Mazel
Journal:  Nat Commun       Date:  2016-03-10       Impact factor: 14.919

  3 in total

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