Multicopy suppressor screens reveal convergent evolution of single-gene lysis proteins.


Journal

Nature chemical biology
ISSN: 1552-4469
Titre abrégé: Nat Chem Biol
Pays: United States
ID NLM: 101231976

Informations de publication

Date de publication:
06 2023
Historique:
received: 18 09 2022
accepted: 18 01 2023
medline: 1 6 2023
pubmed: 23 2 2023
entrez: 22 2 2023
Statut: ppublish

Résumé

Single-strand RNA (ssRNA) Fiersviridae phages cause host lysis with a product of single gene (sgl for single-gene lysis; product Sgl) that induces autolysis. Many different Sgls have been discovered, but the molecular targets of only a few have been identified. In this study, we used a high-throughput genetic screen to uncover genome-wide host suppressors of diverse Sgls. In addition to validating known molecular mechanisms, we discovered that the Sgl of PP7, an ssRNA phage of Pseudomonas aeruginosa, targets MurJ, the flippase responsible for lipid II export, previously shown to be the target of the Sgl of coliphage M. These two Sgls, which are unrelated and predicted to have opposite membrane topology, thus represent a case of convergent evolution. We extended the genetic screens to other uncharacterized Sgls and uncovered a common set of multicopy suppressors, suggesting that these Sgls act by the same or similar mechanism.

Identifiants

pubmed: 36805702
doi: 10.1038/s41589-023-01269-7
pii: 10.1038/s41589-023-01269-7
pmc: PMC10229422
doi:

Banques de données

figshare
['10.6084/m9.figshare.21714296.v2']

Types de publication

Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

759-766

Subventions

Organisme : NIGMS NIH HHS
ID : R35 GM136396
Pays : United States
Organisme : NCRR NIH HHS
ID : S10 RR029668
Pays : United States
Organisme : NCRR NIH HHS
ID : S10 RR027303
Pays : United States

Informations de copyright

© 2023. The Author(s).

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Auteurs

Benjamin A Adler (BA)

The UC Berkeley-UCSF Graduate Program in Bioengineering, Berkeley, CA, USA.
Department of Bioengineering, University of California, Berkeley, Berkeley, CA, USA.
Innovative Genomics Institute, University of California, Berkeley, Berkeley, CA, USA.

Karthik Chamakura (K)

Department of Biochemistry and Biophysics, Center for Phage Technology, Texas A&M University, College Station, TX, USA.
Armata Pharmaceuticals, Inc., Marina Del Rey, CA, USA.

Heloise Carion (H)

Department of Bioengineering, University of California, Berkeley, Berkeley, CA, USA.

Jonathan Krog (J)

Department of Bioengineering, University of California, Berkeley, Berkeley, CA, USA.

Adam M Deutschbauer (AM)

Environmental Genomics and Systems Biology Division, Lawrence Berkeley National Laboratory, Berkeley, CA, USA.

Ry Young (R)

Department of Biochemistry and Biophysics, Center for Phage Technology, Texas A&M University, College Station, TX, USA.

Vivek K Mutalik (VK)

Innovative Genomics Institute, University of California, Berkeley, Berkeley, CA, USA. vkmutalik@lbl.gov.
Environmental Genomics and Systems Biology Division, Lawrence Berkeley National Laboratory, Berkeley, CA, USA. vkmutalik@lbl.gov.

Adam P Arkin (AP)

Department of Bioengineering, University of California, Berkeley, Berkeley, CA, USA. aparkin@lbl.gov.
Innovative Genomics Institute, University of California, Berkeley, Berkeley, CA, USA. aparkin@lbl.gov.
Environmental Genomics and Systems Biology Division, Lawrence Berkeley National Laboratory, Berkeley, CA, USA. aparkin@lbl.gov.

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Classifications MeSH