Cargando…

A transcriptome-wide analysis deciphers distinct roles of G1 cyclins in temporal organization of the yeast cell cycle

Oscillating gene expression is crucial for correct timing and progression through cell cycle. In Saccharomyces cerevisiae, G1 cyclins Cln1–3 are essential drivers of the cell cycle and have an important role for temporal fine-tuning. We measured time-resolved transcriptome-wide gene expression for w...

Descripción completa

Detalles Bibliográficos
Autores principales: Teufel, Lotte, Tummler, Katja, Flöttmann, Max, Herrmann, Andreas, Barkai, Naama, Klipp, Edda
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6399449/
https://www.ncbi.nlm.nih.gov/pubmed/30833602
http://dx.doi.org/10.1038/s41598-019-39850-7
_version_ 1783399765579399168
author Teufel, Lotte
Tummler, Katja
Flöttmann, Max
Herrmann, Andreas
Barkai, Naama
Klipp, Edda
author_facet Teufel, Lotte
Tummler, Katja
Flöttmann, Max
Herrmann, Andreas
Barkai, Naama
Klipp, Edda
author_sort Teufel, Lotte
collection PubMed
description Oscillating gene expression is crucial for correct timing and progression through cell cycle. In Saccharomyces cerevisiae, G1 cyclins Cln1–3 are essential drivers of the cell cycle and have an important role for temporal fine-tuning. We measured time-resolved transcriptome-wide gene expression for wild type and cyclin single and double knockouts over cell cycle with and without osmotic stress. Clustering of expression profiles, peak time detection of oscillating genes, integration with transcription factor network dynamics, and assignment to cell cycle phases allowed us to quantify the effect of genetic or stress perturbations on the duration of cell cycle phases. Cln1 and Cln2 showed functional differences, especially affecting later phases. Deletion of Cln3 led to a delay of START followed by normal progression through later phases. Our data and network analysis suggest mutual effects of cyclins with the transcriptional regulators SBF and MBF.
format Online
Article
Text
id pubmed-6399449
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-63994492019-03-07 A transcriptome-wide analysis deciphers distinct roles of G1 cyclins in temporal organization of the yeast cell cycle Teufel, Lotte Tummler, Katja Flöttmann, Max Herrmann, Andreas Barkai, Naama Klipp, Edda Sci Rep Article Oscillating gene expression is crucial for correct timing and progression through cell cycle. In Saccharomyces cerevisiae, G1 cyclins Cln1–3 are essential drivers of the cell cycle and have an important role for temporal fine-tuning. We measured time-resolved transcriptome-wide gene expression for wild type and cyclin single and double knockouts over cell cycle with and without osmotic stress. Clustering of expression profiles, peak time detection of oscillating genes, integration with transcription factor network dynamics, and assignment to cell cycle phases allowed us to quantify the effect of genetic or stress perturbations on the duration of cell cycle phases. Cln1 and Cln2 showed functional differences, especially affecting later phases. Deletion of Cln3 led to a delay of START followed by normal progression through later phases. Our data and network analysis suggest mutual effects of cyclins with the transcriptional regulators SBF and MBF. Nature Publishing Group UK 2019-03-04 /pmc/articles/PMC6399449/ /pubmed/30833602 http://dx.doi.org/10.1038/s41598-019-39850-7 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Teufel, Lotte
Tummler, Katja
Flöttmann, Max
Herrmann, Andreas
Barkai, Naama
Klipp, Edda
A transcriptome-wide analysis deciphers distinct roles of G1 cyclins in temporal organization of the yeast cell cycle
title A transcriptome-wide analysis deciphers distinct roles of G1 cyclins in temporal organization of the yeast cell cycle
title_full A transcriptome-wide analysis deciphers distinct roles of G1 cyclins in temporal organization of the yeast cell cycle
title_fullStr A transcriptome-wide analysis deciphers distinct roles of G1 cyclins in temporal organization of the yeast cell cycle
title_full_unstemmed A transcriptome-wide analysis deciphers distinct roles of G1 cyclins in temporal organization of the yeast cell cycle
title_short A transcriptome-wide analysis deciphers distinct roles of G1 cyclins in temporal organization of the yeast cell cycle
title_sort transcriptome-wide analysis deciphers distinct roles of g1 cyclins in temporal organization of the yeast cell cycle
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6399449/
https://www.ncbi.nlm.nih.gov/pubmed/30833602
http://dx.doi.org/10.1038/s41598-019-39850-7
work_keys_str_mv AT teufellotte atranscriptomewideanalysisdeciphersdistinctrolesofg1cyclinsintemporalorganizationoftheyeastcellcycle
AT tummlerkatja atranscriptomewideanalysisdeciphersdistinctrolesofg1cyclinsintemporalorganizationoftheyeastcellcycle
AT flottmannmax atranscriptomewideanalysisdeciphersdistinctrolesofg1cyclinsintemporalorganizationoftheyeastcellcycle
AT herrmannandreas atranscriptomewideanalysisdeciphersdistinctrolesofg1cyclinsintemporalorganizationoftheyeastcellcycle
AT barkainaama atranscriptomewideanalysisdeciphersdistinctrolesofg1cyclinsintemporalorganizationoftheyeastcellcycle
AT klippedda atranscriptomewideanalysisdeciphersdistinctrolesofg1cyclinsintemporalorganizationoftheyeastcellcycle
AT teufellotte transcriptomewideanalysisdeciphersdistinctrolesofg1cyclinsintemporalorganizationoftheyeastcellcycle
AT tummlerkatja transcriptomewideanalysisdeciphersdistinctrolesofg1cyclinsintemporalorganizationoftheyeastcellcycle
AT flottmannmax transcriptomewideanalysisdeciphersdistinctrolesofg1cyclinsintemporalorganizationoftheyeastcellcycle
AT herrmannandreas transcriptomewideanalysisdeciphersdistinctrolesofg1cyclinsintemporalorganizationoftheyeastcellcycle
AT barkainaama transcriptomewideanalysisdeciphersdistinctrolesofg1cyclinsintemporalorganizationoftheyeastcellcycle
AT klippedda transcriptomewideanalysisdeciphersdistinctrolesofg1cyclinsintemporalorganizationoftheyeastcellcycle