Revealing the mechanism of repressor inactivation during switching of a temperate bacteriophage.


Journal

Proceedings of the National Academy of Sciences of the United States of America
ISSN: 1091-6490
Titre abrégé: Proc Natl Acad Sci U S A
Pays: United States
ID NLM: 7505876

Informations de publication

Date de publication:
25 08 2020
Historique:
pubmed: 14 8 2020
medline: 23 10 2020
entrez: 14 8 2020
Statut: ppublish

Résumé

Temperate bacteriophages can enter one of two life cycles following infection of a sensitive host: the lysogenic or the lytic life cycle. The choice between the two alternative life cycles is dependent upon a tight regulation of promoters and their cognate regulatory proteins within the phage genome. We investigated the genetic switch of TP901-1, a bacteriophage of

Identifiants

pubmed: 32788352
pii: 2005218117
doi: 10.1073/pnas.2005218117
pmc: PMC7456139
doi:

Substances chimiques

Repressor Proteins 0
Viral Regulatory and Accessory Proteins 0
phage repressor proteins 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

20576-20585

Déclaration de conflit d'intérêts

The authors declare no competing interest.

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Auteurs

Kim Krighaar Rasmussen (KK)

Department of Chemistry, University of Copenhagen, DK-2100 Copenhagen, Denmark.

Andrés Palencia (A)

Institute for Advanced Biosciences, Structural Biology of Novel Drug Targets in Human Diseases, INSERM U1209, CNRS UMR5309, Université Grenoble Alpes, F-38000 Grenoble, France.

Anders K Varming (AK)

Department of Chemistry, University of Copenhagen, DK-2100 Copenhagen, Denmark.

Habiba El-Wali (H)

Metabolic Signaling and Regulation, Department of Systems Biology, Technical University of Denmark, DK-2800 Lyngby, Denmark.

Elisabetta Boeri Erba (E)

Université Grenoble Alpes, Commissariat à l'Energie Atomique et aux Energies Alternatives (CEA), Centre National de la Recherche Scientifique (CNRS), Institut de Biologie Structurale, F-38000 Grenoble, France.

Martin Blackledge (M)

Université Grenoble Alpes, Commissariat à l'Energie Atomique et aux Energies Alternatives (CEA), Centre National de la Recherche Scientifique (CNRS), Institut de Biologie Structurale, F-38000 Grenoble, France.

Karin Hammer (K)

Metabolic Signaling and Regulation, Department of Systems Biology, Technical University of Denmark, DK-2800 Lyngby, Denmark.

Torsten Herrmann (T)

Université Grenoble Alpes, Commissariat à l'Energie Atomique et aux Energies Alternatives (CEA), Centre National de la Recherche Scientifique (CNRS), Institut de Biologie Structurale, F-38000 Grenoble, France.

Mogens Kilstrup (M)

Metabolic Signaling and Regulation, Department of Systems Biology, Technical University of Denmark, DK-2800 Lyngby, Denmark.

Leila Lo Leggio (L)

Department of Chemistry, University of Copenhagen, DK-2100 Copenhagen, Denmark; leila@chem.ku.dk malene.ringkjobing-jensen@ibs.fr.

Malene Ringkjøbing Jensen (MR)

Université Grenoble Alpes, Commissariat à l'Energie Atomique et aux Energies Alternatives (CEA), Centre National de la Recherche Scientifique (CNRS), Institut de Biologie Structurale, F-38000 Grenoble, France leila@chem.ku.dk malene.ringkjobing-jensen@ibs.fr.

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