Skip Navigation


Nucleic Acids Research Advance Access originally published online on September 20, 2007
Nucleic Acids Research 2007 35(19):6475-6489; doi:10.1093/nar/gkm709
This Article
Right arrow Full Text Freely available
Right arrow Print PDF (14778K) Freely available
Right arrow Screen PDF (1318K) Freely available
Right arrow Supplementary Material
Right arrowOA All Versions of this Article:
35/19/6475    most recent
gkm709v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Commercial Re-use Guidelines
for Open Access NAR Content
Google Scholar
Right arrow Articles by Demarre, G.
Right arrow Articles by Mazel, D.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Demarre, G.
Right arrow Articles by Mazel, D.
Social Bookmarking
Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Nucleic Acids Research, 2007, Vol. 35, No. 19 6475-6489
© 2007 The Author(s)
This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

Nucleic Acid Enzymes

Identification of key structural determinants of the IntI1 integron integrase that influence attC x attI1 recombination efficiency

Gaëlle Demarre1, Clara Frumerie1, Deshmukh N. Gopaul2 and Didier Mazel1,*

1Unité Plasticité du Génome Bactérien, CNRS URA 2171 and 2Laboratoire de Biochimie et Biophysique des Macromolécules, CNRS URA 2185, Institut Pasteur, 25 rue du Dr Roux, 75724, Paris 75724, France

*To whom correspondence should be addressed. Tel: +33 1 40 61 32 84; Fax: +33 1 45 68 88 34; Email: mazel{at}pasteur.fr

Received May 25, 2007. Revised August 27, 2007. Accepted August 27, 2007.

The integron platform codes for an integrase (IntI) from the tyrosine family of recombinases that mediates recombination between a proximal double-strand recombination site, attI and a single-strand target recombination site, attC. The attI site is only recognized by its cognate integrase, while the various tested attCs sites are recombined by several different IntI integrases. We have developed a genetic system to enrich and select mutants of IntI1 that provide a higher yield of recombination in order to identify key protein structural elements important for attC x attI1 recombination. We isolated mutants with higher activity on wild type and mutant attC sites. Interestingly, three out of four characterized IntI1 mutants selected on different substrates are mutants of the conserved aspartic acid in position 161. The IntI1 model we made based on the VchIntIA 3D structure suggests that substitution at this position, which plays a central role in multimer assembly, can increase or decrease the stability of the complex and accordingly influence the rate of attI x attC recombination versus attC x attC. These results suggest that there is a balance between the specificity of the protein and the protein/protein interactions in the recombination synapse.

Present address: Gaëlle Demarre, Laboratory of Biochemistry and Molecular Biology, NCI, 37/6044, NIH, Bethesda, MD 20892-4260, USA


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?




Disclaimer:
Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.