Cargando…
From network to phenotype: the dynamic wiring of an Arabidopsis transcriptional network induced by osmotic stress
Plants have established different mechanisms to cope with environmental fluctuations and accordingly fine‐tune their growth and development through the regulation of complex molecular networks. It is largely unknown how the network architectures change and what the key regulators in stress responses...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5740496/ https://www.ncbi.nlm.nih.gov/pubmed/29269383 http://dx.doi.org/10.15252/msb.20177840 |
_version_ | 1783288040279506944 |
---|---|
author | Van den Broeck, Lisa Dubois, Marieke Vermeersch, Mattias Storme, Veronique Matsui, Minami Inzé, Dirk |
author_facet | Van den Broeck, Lisa Dubois, Marieke Vermeersch, Mattias Storme, Veronique Matsui, Minami Inzé, Dirk |
author_sort | Van den Broeck, Lisa |
collection | PubMed |
description | Plants have established different mechanisms to cope with environmental fluctuations and accordingly fine‐tune their growth and development through the regulation of complex molecular networks. It is largely unknown how the network architectures change and what the key regulators in stress responses and plant growth are. Here, we investigated a complex, highly interconnected network of 20 Arabidopsis transcription factors (TFs) at the basis of leaf growth inhibition upon mild osmotic stress. We tracked the dynamic behavior of the stress‐responsive TFs over time, showing the rapid induction following stress treatment, specifically in growing leaves. The connections between the TFs were uncovered using inducible overexpression lines and were validated with transient expression assays. This study resulted in the identification of a core network, composed of ERF6, ERF8, ERF9, ERF59, and ERF98, which is responsible for most transcriptional connections. The analyses highlight the biological function of this core network in environmental adaptation and its redundancy. Finally, a phenotypic analysis of loss‐of‐function and gain‐of‐function lines of the transcription factors established multiple connections between the stress‐responsive network and leaf growth. |
format | Online Article Text |
id | pubmed-5740496 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-57404962018-01-02 From network to phenotype: the dynamic wiring of an Arabidopsis transcriptional network induced by osmotic stress Van den Broeck, Lisa Dubois, Marieke Vermeersch, Mattias Storme, Veronique Matsui, Minami Inzé, Dirk Mol Syst Biol Articles Plants have established different mechanisms to cope with environmental fluctuations and accordingly fine‐tune their growth and development through the regulation of complex molecular networks. It is largely unknown how the network architectures change and what the key regulators in stress responses and plant growth are. Here, we investigated a complex, highly interconnected network of 20 Arabidopsis transcription factors (TFs) at the basis of leaf growth inhibition upon mild osmotic stress. We tracked the dynamic behavior of the stress‐responsive TFs over time, showing the rapid induction following stress treatment, specifically in growing leaves. The connections between the TFs were uncovered using inducible overexpression lines and were validated with transient expression assays. This study resulted in the identification of a core network, composed of ERF6, ERF8, ERF9, ERF59, and ERF98, which is responsible for most transcriptional connections. The analyses highlight the biological function of this core network in environmental adaptation and its redundancy. Finally, a phenotypic analysis of loss‐of‐function and gain‐of‐function lines of the transcription factors established multiple connections between the stress‐responsive network and leaf growth. John Wiley and Sons Inc. 2017-12-21 /pmc/articles/PMC5740496/ /pubmed/29269383 http://dx.doi.org/10.15252/msb.20177840 Text en © 2017 The Authors. Published under the terms of the CC BY 4.0 license This is an open access article under the terms of the Creative Commons Attribution 4.0 (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Articles Van den Broeck, Lisa Dubois, Marieke Vermeersch, Mattias Storme, Veronique Matsui, Minami Inzé, Dirk From network to phenotype: the dynamic wiring of an Arabidopsis transcriptional network induced by osmotic stress |
title | From network to phenotype: the dynamic wiring of an Arabidopsis transcriptional network induced by osmotic stress |
title_full | From network to phenotype: the dynamic wiring of an Arabidopsis transcriptional network induced by osmotic stress |
title_fullStr | From network to phenotype: the dynamic wiring of an Arabidopsis transcriptional network induced by osmotic stress |
title_full_unstemmed | From network to phenotype: the dynamic wiring of an Arabidopsis transcriptional network induced by osmotic stress |
title_short | From network to phenotype: the dynamic wiring of an Arabidopsis transcriptional network induced by osmotic stress |
title_sort | from network to phenotype: the dynamic wiring of an arabidopsis transcriptional network induced by osmotic stress |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5740496/ https://www.ncbi.nlm.nih.gov/pubmed/29269383 http://dx.doi.org/10.15252/msb.20177840 |
work_keys_str_mv | AT vandenbroecklisa fromnetworktophenotypethedynamicwiringofanarabidopsistranscriptionalnetworkinducedbyosmoticstress AT duboismarieke fromnetworktophenotypethedynamicwiringofanarabidopsistranscriptionalnetworkinducedbyosmoticstress AT vermeerschmattias fromnetworktophenotypethedynamicwiringofanarabidopsistranscriptionalnetworkinducedbyosmoticstress AT stormeveronique fromnetworktophenotypethedynamicwiringofanarabidopsistranscriptionalnetworkinducedbyosmoticstress AT matsuiminami fromnetworktophenotypethedynamicwiringofanarabidopsistranscriptionalnetworkinducedbyosmoticstress AT inzedirk fromnetworktophenotypethedynamicwiringofanarabidopsistranscriptionalnetworkinducedbyosmoticstress |