The proteomic landscape of genome-wide genetic perturbations.

Saccharomyces cerevisiae data-independent acquisition deletion functional genomics functional proteomics gene annotation high throughput knockout quantitative proteomics systems biology

Journal

Cell
ISSN: 1097-4172
Titre abrégé: Cell
Pays: United States
ID NLM: 0413066

Informations de publication

Date de publication:
27 04 2023
Historique:
received: 17 05 2022
revised: 20 01 2023
accepted: 21 03 2023
medline: 1 5 2023
pubmed: 21 4 2023
entrez: 20 04 2023
Statut: ppublish

Résumé

Functional genomic strategies have become fundamental for annotating gene function and regulatory networks. Here, we combined functional genomics with proteomics by quantifying protein abundances in a genome-scale knockout library in Saccharomyces cerevisiae, using data-independent acquisition mass spectrometry. We find that global protein expression is driven by a complex interplay of (1) general biological properties, including translation rate, protein turnover, the formation of protein complexes, growth rate, and genome architecture, followed by (2) functional properties, such as the connectivity of a protein in genetic, metabolic, and physical interaction networks. Moreover, we show that functional proteomics complements current gene annotation strategies through the assessment of proteome profile similarity, protein covariation, and reverse proteome profiling. Thus, our study reveals principles that govern protein expression and provides a genome-spanning resource for functional annotation.

Identifiants

pubmed: 37080200
pii: S0092-8674(23)00300-8
doi: 10.1016/j.cell.2023.03.026
pii:
doi:

Substances chimiques

Proteome 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

2018-2034.e21

Subventions

Organisme : Biotechnology and Biological Sciences Research Council
ID : BB/N015215/1
Pays : United Kingdom
Organisme : Biotechnology and Biological Sciences Research Council
ID : BB/N015282/1
Pays : United Kingdom
Organisme : Wellcome Trust
ID : FC001134
Pays : United Kingdom
Organisme : Cancer Research UK
Pays : United Kingdom
Organisme : Medical Research Council
Pays : United Kingdom
Organisme : Wellcome Trust
ID : IA 200829/Z/16/Z
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/T03050X/1
Pays : United Kingdom

Informations de copyright

Copyright © 2023 The Author(s). Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of interests The authors declare no competing interests.

Auteurs

Christoph B Messner (CB)

The Francis Crick Institute, Molecular Biology of Metabolism Laboratory, London NW1 1AT, UK; Precision Proteomics Center, Swiss Institute of Allergy and Asthma Research (SIAF), University of Zurich, 7265 Davos, Switzerland.

Vadim Demichev (V)

The Francis Crick Institute, Molecular Biology of Metabolism Laboratory, London NW1 1AT, UK; Charité Universitätsmedizin Berlin, Department of Biochemistry, 10117 Berlin, Germany; Department of Biochemistry, Cambridge Centre for Proteomics, University of Cambridge, Cambridge CB2 1QW, UK.

Julia Muenzner (J)

Charité Universitätsmedizin Berlin, Department of Biochemistry, 10117 Berlin, Germany.

Simran K Aulakh (SK)

The Francis Crick Institute, Molecular Biology of Metabolism Laboratory, London NW1 1AT, UK.

Natalie Barthel (N)

Charité Universitätsmedizin Berlin, Department of Biochemistry, 10117 Berlin, Germany.

Annika Röhl (A)

Charité Universitätsmedizin Berlin, Department of Biochemistry, 10117 Berlin, Germany.

Lucía Herrera-Domínguez (L)

Charité Universitätsmedizin Berlin, Department of Biochemistry, 10117 Berlin, Germany.

Anna-Sophia Egger (AS)

The Francis Crick Institute, Molecular Biology of Metabolism Laboratory, London NW1 1AT, UK.

Stephan Kamrad (S)

The Francis Crick Institute, Molecular Biology of Metabolism Laboratory, London NW1 1AT, UK.

Jing Hou (J)

The Donnelly Centre, University of Toronto, Toronto, ON M5S3E1, Canada.

Guihong Tan (G)

The Donnelly Centre, University of Toronto, Toronto, ON M5S3E1, Canada.

Oliver Lemke (O)

Charité Universitätsmedizin Berlin, Department of Biochemistry, 10117 Berlin, Germany.

Enrica Calvani (E)

The Francis Crick Institute, Molecular Biology of Metabolism Laboratory, London NW1 1AT, UK.

Lukasz Szyrwiel (L)

The Francis Crick Institute, Molecular Biology of Metabolism Laboratory, London NW1 1AT, UK; Charité Universitätsmedizin Berlin, Department of Biochemistry, 10117 Berlin, Germany.

Michael Mülleder (M)

Charité Universitätsmedizin, Core Facility - High Throughput Mass Spectrometry, 10117 Berlin, Germany.

Kathryn S Lilley (KS)

Department of Biochemistry, Cambridge Centre for Proteomics, University of Cambridge, Cambridge CB2 1QW, UK.

Charles Boone (C)

Department of Molecular Genetics, University of Toronto, Toronto, ON M5S3E1, Canada; The Donnelly Centre, University of Toronto, Toronto, ON M5S3E1, Canada; RIKEN Center for Sustainable Resource Science, Wako, 351-0198 Saitama, Japan.

Georg Kustatscher (G)

Wellcome Centre for Cell Biology, University of Edinburgh, Max Born Crescent, Edinburgh EH9 3BF, Scotland, UK. Electronic address: georg.kustatscher@ed.ac.uk.

Markus Ralser (M)

The Francis Crick Institute, Molecular Biology of Metabolism Laboratory, London NW1 1AT, UK; Charité Universitätsmedizin Berlin, Department of Biochemistry, 10117 Berlin, Germany; The Wellcome Centre for Human Genetics, Nuffield Department of Medicine, University of Oxford, Oxford OX3 7BN, UK; Max Planck Institute for Molecular Genetics, 14195 Berlin, Germany. Electronic address: markus.ralser@charite.de.

Articles similaires

Coal Metagenome Phylogeny Bacteria Genome, Bacterial
Genome, Bacterial Virulence Phylogeny Genomics Plant Diseases
Humans Arthritis, Rheumatoid Lipid Metabolism Male Female

Classifications MeSH