The reverse gyrase TopR1 is responsible for the homeostatic control of DNA supercoiling in the hyperthermophilic archaeon Sulfolobus solfataricus.


Journal

Molecular microbiology
ISSN: 1365-2958
Titre abrégé: Mol Microbiol
Pays: England
ID NLM: 8712028

Informations de publication

Date de publication:
02 2020
Historique:
received: 01 08 2019
revised: 06 11 2019
accepted: 10 11 2019
pubmed: 13 11 2019
medline: 11 11 2020
entrez: 13 11 2019
Statut: ppublish

Résumé

Maintaining an appropriate DNA topology with DNA-based processes (DNA replication, transcription and recombination) is crucial for all three domains of life. In bacteria, the homeostatic regulation for controlling DNA supercoiling relies on antagonistic activities of two DNA topoisomerases, TopoI and gyrase. In hyperthermophilic crenarchaea, the presence of such a regulatory system is suggested as two DNA topoisomerases, TopoVI and reverse gyrase, catalyze antagonistic activities. To test this hypothesis, we estimated and compared the number of the TopoVI with that of the two reverse gyrases, TopR1 and TopR2, in Sulfolobus solfataricus cells maintained either at 80 or at 88°C, or reciprocally shifted from one temperature to the other. From the three DNA topoisomerases, TopR1 is the only one exhibiting significant quantitative variations in response to the up- and down-shifts. In addition, the corresponding intrinsic activities of these three DNA topoisomerases were tested in vitro at both temperatures. Although temperature modulates the three DNA topoisomerases activities, TopR1 is the sole topoisomerase able to function at high temperature. Altogether, results presented in this study demonstrate, for the first time, that the DNA topological state of a crenarchaeon is regulated via a homeostatic control, which is mainly mediated by the fine-tuning of TopR1.

Identifiants

pubmed: 31713907
doi: 10.1111/mmi.14424
doi:

Substances chimiques

Archaeal Proteins 0
DNA, Bacterial 0
DNA, Superhelical 0
DNA Topoisomerases EC 5.99.1.-
DNA topoisomerase VI EC 5.99.1.-
DNA Topoisomerases, Type II EC 5.99.1.3

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

356-368

Informations de copyright

© 2019 John Wiley & Sons Ltd.

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Auteurs

Mohea Couturier (M)

Institut de Génétique et Microbiologie, UMR 8621 CNRS-Université Paris-Sud, Orsay Cedex, France.

Danièle Gadelle (D)

Institut de Génétique et Microbiologie, UMR 8621 CNRS-Université Paris-Sud, Orsay Cedex, France.

Patrick Forterre (P)

Institut de Génétique et Microbiologie, UMR 8621 CNRS-Université Paris-Sud, Orsay Cedex, France.

Marc Nadal (M)

Institut de Génétique et Microbiologie, UMR 8621 CNRS-Université Paris-Sud, Orsay Cedex, France.
Institut Jacques Monod, UMR 8621 CNRS-Université Paris Diderot, Paris Cedex 13, France.

Florence Garnier (F)

Institut de Génétique et Microbiologie, UMR 8621 CNRS-Université Paris-Sud, Orsay Cedex, France.
Institut Jacques Monod, UMR 8621 CNRS-Université Paris Diderot, Paris Cedex 13, France.
Biology Department, Université Versailles St-Quentin, Versailles, France.

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