Cargando…
Cell cycle population effects in perturbation studies
Growth condition perturbation or gene function disruption are commonly used strategies to study cellular systems. Although it is widely appreciated that such experiments may involve indirect effects, these frequently remain uncharacterized. Here, analysis of functionally unrelated Saccharyomyces cer...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4265054/ https://www.ncbi.nlm.nih.gov/pubmed/24952590 http://dx.doi.org/10.15252/msb.20145172 |
_version_ | 1782348817282105344 |
---|---|
author | O'Duibhir, Eoghan Lijnzaad, Philip Benschop, Joris J Lenstra, Tineke L van Leenen, Dik Groot Koerkamp, Marian JA Margaritis, Thanasis Brok, Mariel O Kemmeren, Patrick Holstege, Frank CP |
author_facet | O'Duibhir, Eoghan Lijnzaad, Philip Benschop, Joris J Lenstra, Tineke L van Leenen, Dik Groot Koerkamp, Marian JA Margaritis, Thanasis Brok, Mariel O Kemmeren, Patrick Holstege, Frank CP |
author_sort | O'Duibhir, Eoghan |
collection | PubMed |
description | Growth condition perturbation or gene function disruption are commonly used strategies to study cellular systems. Although it is widely appreciated that such experiments may involve indirect effects, these frequently remain uncharacterized. Here, analysis of functionally unrelated Saccharyomyces cerevisiae deletion strains reveals a common gene expression signature. One property shared by these strains is slower growth, with increased presence of the signature in more slowly growing strains. The slow growth signature is highly similar to the environmental stress response (ESR), an expression response common to diverse environmental perturbations. Both environmental and genetic perturbations result in growth rate changes. These are accompanied by a change in the distribution of cells over different cell cycle phases. Rather than representing a direct expression response in single cells, both the slow growth signature and ESR mainly reflect a redistribution of cells over different cell cycle phases, primarily characterized by an increase in the G1 population. The findings have implications for any study of perturbation that is accompanied by growth rate changes. Strategies to counter these effects are presented and discussed. |
format | Online Article Text |
id | pubmed-4265054 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Blackwell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-42650542014-12-24 Cell cycle population effects in perturbation studies O'Duibhir, Eoghan Lijnzaad, Philip Benschop, Joris J Lenstra, Tineke L van Leenen, Dik Groot Koerkamp, Marian JA Margaritis, Thanasis Brok, Mariel O Kemmeren, Patrick Holstege, Frank CP Mol Syst Biol Articles Growth condition perturbation or gene function disruption are commonly used strategies to study cellular systems. Although it is widely appreciated that such experiments may involve indirect effects, these frequently remain uncharacterized. Here, analysis of functionally unrelated Saccharyomyces cerevisiae deletion strains reveals a common gene expression signature. One property shared by these strains is slower growth, with increased presence of the signature in more slowly growing strains. The slow growth signature is highly similar to the environmental stress response (ESR), an expression response common to diverse environmental perturbations. Both environmental and genetic perturbations result in growth rate changes. These are accompanied by a change in the distribution of cells over different cell cycle phases. Rather than representing a direct expression response in single cells, both the slow growth signature and ESR mainly reflect a redistribution of cells over different cell cycle phases, primarily characterized by an increase in the G1 population. The findings have implications for any study of perturbation that is accompanied by growth rate changes. Strategies to counter these effects are presented and discussed. Blackwell Publishing Ltd 2014-07-01 /pmc/articles/PMC4265054/ /pubmed/24952590 http://dx.doi.org/10.15252/msb.20145172 Text en © 2014 The Authors. Published under the terms of the CC BY 4.0 license http://creativecommons.org/licenses/by/4.0/ This is an open access article under the terms of the Creative Commons Attribution 4.0 License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Articles O'Duibhir, Eoghan Lijnzaad, Philip Benschop, Joris J Lenstra, Tineke L van Leenen, Dik Groot Koerkamp, Marian JA Margaritis, Thanasis Brok, Mariel O Kemmeren, Patrick Holstege, Frank CP Cell cycle population effects in perturbation studies |
title | Cell cycle population effects in perturbation studies |
title_full | Cell cycle population effects in perturbation studies |
title_fullStr | Cell cycle population effects in perturbation studies |
title_full_unstemmed | Cell cycle population effects in perturbation studies |
title_short | Cell cycle population effects in perturbation studies |
title_sort | cell cycle population effects in perturbation studies |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4265054/ https://www.ncbi.nlm.nih.gov/pubmed/24952590 http://dx.doi.org/10.15252/msb.20145172 |
work_keys_str_mv | AT oduibhireoghan cellcyclepopulationeffectsinperturbationstudies AT lijnzaadphilip cellcyclepopulationeffectsinperturbationstudies AT benschopjorisj cellcyclepopulationeffectsinperturbationstudies AT lenstratinekel cellcyclepopulationeffectsinperturbationstudies AT vanleenendik cellcyclepopulationeffectsinperturbationstudies AT grootkoerkampmarianja cellcyclepopulationeffectsinperturbationstudies AT margaritisthanasis cellcyclepopulationeffectsinperturbationstudies AT brokmarielo cellcyclepopulationeffectsinperturbationstudies AT kemmerenpatrick cellcyclepopulationeffectsinperturbationstudies AT holstegefrankcp cellcyclepopulationeffectsinperturbationstudies |