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
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.e21Subventions
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.