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Published on: June 25, 2013
Bacteriophage mv4 site-specific recombination: the central role of the P2 mv4Int-binding site
Michèle Coddeville1, Jean-François Spinella, Pauline Cassart
1Université de Toulouse, Université Paul Sabatier, Laboratoire de Microbiologie et de Génétique Moléculaires, Toulouse, France.
Abstract:
The contributions of the five (mv4)Int- and two (mv4)Xis arm-binding sites to the spatial intasome organization of bacteriophage mv4 were found not to be equivalent. The 8-bp overlap region was mapped to the left extremity of the core region and is directly flanked by the P2 Int arm-binding site. These results and the absence of characteristic Int core-binding sites suggest that the P2 site is the determinant for integrase positioning and recognition of the core region.
Insights
The study reveals unequal contributions of bacteriophage mv4 arm-binding sites to intasome organization. The P2 Int arm-binding site, flanking the overlap region, appears crucial for integrase positioning and core region recognition.
Area of Science:
- Molecular Biology
- Virology
- Genetics
Background:
- Bacteriophage mv4 integrase (Int) mediates DNA integration.
- Intasome organization is critical for site-specific recombination.
- Understanding Int binding sites is key to elucidating recombination mechanisms.
Purpose of the Study:
- To investigate the roles of mv4 Int and Xis arm-binding sites in spatial intasome organization.
- To map the 8-bp overlap region and its flanking sequences.
- To determine the significance of the P2 Int arm-binding site in integrase recognition.
Main Methods:
- Analysis of bacteriophage mv4 arm-binding sites.
- Mapping of the 8-bp overlap region within the core region.
- Investigating the influence of the P2 Int arm-binding site.
Main Results:
- The five mv4 Int and two mv4 Xis arm-binding sites exhibit non-equivalent contributions to intasome organization.
- The 8-bp overlap region was localized to the left extremity of the core region.
- The P2 Int arm-binding site directly flanks the overlap region and lacks characteristic Int core-binding sites.
Conclusions:
- The P2 Int arm-binding site is a key determinant for integrase positioning.
- The P2 site likely dictates recognition of the core region, independent of canonical Int core-binding sites.
- This finding advances the understanding of bacteriophage DNA integration mechanisms.
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