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PhaeoNet: A Holistic RNAseq-Based Portrait of Transcriptional Coordination in the Model Diatom Phaeodactylum tricornutum
Transcriptional coordination is a fundamental component of prokaryotic and eukaryotic cell biology, underpinning the cell cycle, physiological transitions, and facilitating holistic responses to environmental stress, but its overall dynamics in eukaryotic algae remain poorly understood. Better under...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7596299/ https://www.ncbi.nlm.nih.gov/pubmed/33178253 http://dx.doi.org/10.3389/fpls.2020.590949 |
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author | Ait-Mohamed, Ouardia Novák Vanclová, Anna M. G. Joli, Nathalie Liang, Yue Zhao, Xue Genovesio, Auguste Tirichine, Leila Bowler, Chris Dorrell, Richard G. |
author_facet | Ait-Mohamed, Ouardia Novák Vanclová, Anna M. G. Joli, Nathalie Liang, Yue Zhao, Xue Genovesio, Auguste Tirichine, Leila Bowler, Chris Dorrell, Richard G. |
author_sort | Ait-Mohamed, Ouardia |
collection | PubMed |
description | Transcriptional coordination is a fundamental component of prokaryotic and eukaryotic cell biology, underpinning the cell cycle, physiological transitions, and facilitating holistic responses to environmental stress, but its overall dynamics in eukaryotic algae remain poorly understood. Better understanding of transcriptional partitioning may provide key insights into the primary metabolism pathways of eukaryotic algae, which frequently depend on intricate metabolic associations between the chloroplasts and mitochondria that are not found in plants. Here, we exploit 187 publically available RNAseq datasets generated under varying nitrogen, iron and phosphate growth conditions to understand the co-regulatory principles underpinning transcription in the model diatom Phaeodactylum tricornutum. Using WGCNA (Weighted Gene Correlation Network Analysis), we identify 28 merged modules of co-expressed genes in the P. tricornutum genome, which show high connectivity and correlate well with previous microarray-based surveys of gene co-regulation in this species. We use combined functional, subcellular localization and evolutionary annotations to reveal the fundamental principles underpinning the transcriptional co-regulation of genes implicated in P. tricornutum chloroplast and mitochondrial metabolism, as well as the functions of diverse transcription factors underpinning this co-regulation. The resource is publically available as PhaeoNet, an advanced tool to understand diatom gene co-regulation. |
format | Online Article Text |
id | pubmed-7596299 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-75962992020-11-10 PhaeoNet: A Holistic RNAseq-Based Portrait of Transcriptional Coordination in the Model Diatom Phaeodactylum tricornutum Ait-Mohamed, Ouardia Novák Vanclová, Anna M. G. Joli, Nathalie Liang, Yue Zhao, Xue Genovesio, Auguste Tirichine, Leila Bowler, Chris Dorrell, Richard G. Front Plant Sci Plant Science Transcriptional coordination is a fundamental component of prokaryotic and eukaryotic cell biology, underpinning the cell cycle, physiological transitions, and facilitating holistic responses to environmental stress, but its overall dynamics in eukaryotic algae remain poorly understood. Better understanding of transcriptional partitioning may provide key insights into the primary metabolism pathways of eukaryotic algae, which frequently depend on intricate metabolic associations between the chloroplasts and mitochondria that are not found in plants. Here, we exploit 187 publically available RNAseq datasets generated under varying nitrogen, iron and phosphate growth conditions to understand the co-regulatory principles underpinning transcription in the model diatom Phaeodactylum tricornutum. Using WGCNA (Weighted Gene Correlation Network Analysis), we identify 28 merged modules of co-expressed genes in the P. tricornutum genome, which show high connectivity and correlate well with previous microarray-based surveys of gene co-regulation in this species. We use combined functional, subcellular localization and evolutionary annotations to reveal the fundamental principles underpinning the transcriptional co-regulation of genes implicated in P. tricornutum chloroplast and mitochondrial metabolism, as well as the functions of diverse transcription factors underpinning this co-regulation. The resource is publically available as PhaeoNet, an advanced tool to understand diatom gene co-regulation. Frontiers Media S.A. 2020-10-16 /pmc/articles/PMC7596299/ /pubmed/33178253 http://dx.doi.org/10.3389/fpls.2020.590949 Text en Copyright © 2020 Ait-Mohamed, Novák Vanclová, Joli, Liang, Zhao, Genovesio, Tirichine, Bowler and Dorrell. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Plant Science Ait-Mohamed, Ouardia Novák Vanclová, Anna M. G. Joli, Nathalie Liang, Yue Zhao, Xue Genovesio, Auguste Tirichine, Leila Bowler, Chris Dorrell, Richard G. PhaeoNet: A Holistic RNAseq-Based Portrait of Transcriptional Coordination in the Model Diatom Phaeodactylum tricornutum |
title | PhaeoNet: A Holistic RNAseq-Based Portrait of Transcriptional Coordination in the Model Diatom Phaeodactylum tricornutum |
title_full | PhaeoNet: A Holistic RNAseq-Based Portrait of Transcriptional Coordination in the Model Diatom Phaeodactylum tricornutum |
title_fullStr | PhaeoNet: A Holistic RNAseq-Based Portrait of Transcriptional Coordination in the Model Diatom Phaeodactylum tricornutum |
title_full_unstemmed | PhaeoNet: A Holistic RNAseq-Based Portrait of Transcriptional Coordination in the Model Diatom Phaeodactylum tricornutum |
title_short | PhaeoNet: A Holistic RNAseq-Based Portrait of Transcriptional Coordination in the Model Diatom Phaeodactylum tricornutum |
title_sort | phaeonet: a holistic rnaseq-based portrait of transcriptional coordination in the model diatom phaeodactylum tricornutum |
topic | Plant Science |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7596299/ https://www.ncbi.nlm.nih.gov/pubmed/33178253 http://dx.doi.org/10.3389/fpls.2020.590949 |
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