Cargando…
Growth-rate-dependent and nutrient-specific gene expression resource allocation in fission yeast
Cellular resources are limited and their relative allocation to gene expression programmes determines physiological states and global properties such as the growth rate. Here, we determined the importance of the growth rate in explaining relative changes in protein and mRNA levels in the simple euka...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Life Science Alliance LLC
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8886410/ https://www.ncbi.nlm.nih.gov/pubmed/35228260 http://dx.doi.org/10.26508/lsa.202101223 |
_version_ | 1784660658391875584 |
---|---|
author | Kleijn, Istvan T Martínez-Segura, Amalia Bertaux, François Saint, Malika Kramer, Holger Shahrezaei, Vahid Marguerat, Samuel |
author_facet | Kleijn, Istvan T Martínez-Segura, Amalia Bertaux, François Saint, Malika Kramer, Holger Shahrezaei, Vahid Marguerat, Samuel |
author_sort | Kleijn, Istvan T |
collection | PubMed |
description | Cellular resources are limited and their relative allocation to gene expression programmes determines physiological states and global properties such as the growth rate. Here, we determined the importance of the growth rate in explaining relative changes in protein and mRNA levels in the simple eukaryote Schizosaccharomyces pombe grown on non-limiting nitrogen sources. Although expression of half of fission yeast genes was significantly correlated with the growth rate, this came alongside wide-spread nutrient-specific regulation. Proteome and transcriptome often showed coordinated regulation but with notable exceptions, such as metabolic enzymes. Genes positively correlated with growth rate participated in every level of protein production apart from RNA polymerase II–dependent transcription. Negatively correlated genes belonged mainly to the environmental stress response programme. Critically, metabolic enzymes, which represent ∼55–70% of the proteome by mass, showed mostly condition-specific regulation. In summary, we provide a rich account of resource allocation to gene expression in a simple eukaryote, advancing our basic understanding of the interplay between growth-rate-dependent and nutrient-specific gene expression. |
format | Online Article Text |
id | pubmed-8886410 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Life Science Alliance LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-88864102022-03-14 Growth-rate-dependent and nutrient-specific gene expression resource allocation in fission yeast Kleijn, Istvan T Martínez-Segura, Amalia Bertaux, François Saint, Malika Kramer, Holger Shahrezaei, Vahid Marguerat, Samuel Life Sci Alliance Research Articles Cellular resources are limited and their relative allocation to gene expression programmes determines physiological states and global properties such as the growth rate. Here, we determined the importance of the growth rate in explaining relative changes in protein and mRNA levels in the simple eukaryote Schizosaccharomyces pombe grown on non-limiting nitrogen sources. Although expression of half of fission yeast genes was significantly correlated with the growth rate, this came alongside wide-spread nutrient-specific regulation. Proteome and transcriptome often showed coordinated regulation but with notable exceptions, such as metabolic enzymes. Genes positively correlated with growth rate participated in every level of protein production apart from RNA polymerase II–dependent transcription. Negatively correlated genes belonged mainly to the environmental stress response programme. Critically, metabolic enzymes, which represent ∼55–70% of the proteome by mass, showed mostly condition-specific regulation. In summary, we provide a rich account of resource allocation to gene expression in a simple eukaryote, advancing our basic understanding of the interplay between growth-rate-dependent and nutrient-specific gene expression. Life Science Alliance LLC 2022-02-28 /pmc/articles/PMC8886410/ /pubmed/35228260 http://dx.doi.org/10.26508/lsa.202101223 Text en © 2022 Kleijn et al. https://creativecommons.org/licenses/by/4.0/This article is available under a Creative Commons License (Attribution 4.0 International, as described at https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Research Articles Kleijn, Istvan T Martínez-Segura, Amalia Bertaux, François Saint, Malika Kramer, Holger Shahrezaei, Vahid Marguerat, Samuel Growth-rate-dependent and nutrient-specific gene expression resource allocation in fission yeast |
title | Growth-rate-dependent and nutrient-specific gene expression resource allocation in fission yeast |
title_full | Growth-rate-dependent and nutrient-specific gene expression resource allocation in fission yeast |
title_fullStr | Growth-rate-dependent and nutrient-specific gene expression resource allocation in fission yeast |
title_full_unstemmed | Growth-rate-dependent and nutrient-specific gene expression resource allocation in fission yeast |
title_short | Growth-rate-dependent and nutrient-specific gene expression resource allocation in fission yeast |
title_sort | growth-rate-dependent and nutrient-specific gene expression resource allocation in fission yeast |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8886410/ https://www.ncbi.nlm.nih.gov/pubmed/35228260 http://dx.doi.org/10.26508/lsa.202101223 |
work_keys_str_mv | AT kleijnistvant growthratedependentandnutrientspecificgeneexpressionresourceallocationinfissionyeast AT martinezseguraamalia growthratedependentandnutrientspecificgeneexpressionresourceallocationinfissionyeast AT bertauxfrancois growthratedependentandnutrientspecificgeneexpressionresourceallocationinfissionyeast AT saintmalika growthratedependentandnutrientspecificgeneexpressionresourceallocationinfissionyeast AT kramerholger growthratedependentandnutrientspecificgeneexpressionresourceallocationinfissionyeast AT shahrezaeivahid growthratedependentandnutrientspecificgeneexpressionresourceallocationinfissionyeast AT margueratsamuel growthratedependentandnutrientspecificgeneexpressionresourceallocationinfissionyeast |