A model for the molecular organisation of the IS911 transpososome. - Université Toulouse III - Paul Sabatier - Toulouse INP Accéder directement au contenu
Article Dans Une Revue Mobile DNA Année : 2010

A model for the molecular organisation of the IS911 transpososome.

Résumé

Tight regulation of transposition activity is essential to limit damage transposons may cause by generating potentially lethal DNA rearrangements. Assembly of a bona fide protein-DNA complex, the transpososome, within which transposition is catalysed, is a crucial checkpoint in this regulation. In the case of IS911, a member of the large IS3 bacterial insertion sequence family, the transpososome (synaptic complex A; SCA) is composed of the right and left inverted repeated DNA sequences (IRR and IRL) bridged by the transposase, OrfAB (the IS911-encoded enzyme that catalyses transposition). To characterise further this important protein-DNA complex in vitro, we used different tagged and/or truncated transposase forms and analysed their interaction with IS911 ends using gel electrophoresis. Our results allow us to propose a model in which SCA is assembled with a dimeric form of the transposase. Furthermore, we present atomic force microscopy results showing that the terminal inverted repeat sequences are probably assembled in a parallel configuration within the SCA. These results represent the first step in the structural description of the IS911 transpososome, and are discussed in comparison with the very few other transpososome examples described in the literature.
Fichier principal
Vignette du fichier
1759-8753-1-16.pdf (1.23 Mo) Télécharger le fichier
Origine : Fichiers éditeurs autorisés sur une archive ouverte

Dates et versions

hal-00506948 , version 1 (22-03-2021)

Identifiants

  • HAL Id : hal-00506948 , version 1

Citer

P. Philippe Rousseau, C. Tardin, N. Tolou, L. Salomé, M. Chandler. A model for the molecular organisation of the IS911 transpososome.. Mobile DNA, 2010, 1, pp.16. ⟨hal-00506948⟩
24 Consultations
24 Téléchargements

Partager

Gmail Facebook X LinkedIn More