Cargando…

Extensive tissue-specific transcriptomic plasticity in maize primary roots upon water deficit

Water deficit is the most important environmental constraint severely limiting global crop growth and productivity. This study investigated early transcriptome changes in maize (Zea mays L.) primary root tissues in response to moderate water deficit conditions by RNA-Sequencing. Differential gene ex...

Descripción completa

Detalles Bibliográficos
Autores principales: Opitz, Nina, Marcon, Caroline, Paschold, Anja, Malik, Waqas Ahmed, Lithio, Andrew, Brandt, Ronny, Piepho, Hans-Peter, Nettleton, Dan, Hochholdinger, Frank
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4753846/
https://www.ncbi.nlm.nih.gov/pubmed/26463995
http://dx.doi.org/10.1093/jxb/erv453
_version_ 1782415923073777664
author Opitz, Nina
Marcon, Caroline
Paschold, Anja
Malik, Waqas Ahmed
Lithio, Andrew
Brandt, Ronny
Piepho, Hans-Peter
Nettleton, Dan
Hochholdinger, Frank
author_facet Opitz, Nina
Marcon, Caroline
Paschold, Anja
Malik, Waqas Ahmed
Lithio, Andrew
Brandt, Ronny
Piepho, Hans-Peter
Nettleton, Dan
Hochholdinger, Frank
author_sort Opitz, Nina
collection PubMed
description Water deficit is the most important environmental constraint severely limiting global crop growth and productivity. This study investigated early transcriptome changes in maize (Zea mays L.) primary root tissues in response to moderate water deficit conditions by RNA-Sequencing. Differential gene expression analyses revealed a high degree of plasticity of the water deficit response. The activity status of genes (active/inactive) was determined by a Bayesian hierarchical model. In total, 70% of expressed genes were constitutively active in all tissues. In contrast, <3% (50 genes) of water deficit-responsive genes (1915) were consistently regulated in all tissues, while >75% (1501 genes) were specifically regulated in a single root tissue. Water deficit-responsive genes were most numerous in the cortex of the mature root zone and in the elongation zone. The most prominent functional categories among differentially expressed genes in all tissues were ‘transcriptional regulation’ and ‘hormone metabolism’, indicating global reprogramming of cellular metabolism as an adaptation to water deficit. Additionally, the most significant transcriptomic changes in the root tip were associated with cell wall reorganization, leading to continued root growth despite water deficit conditions. This study provides insight into tissue-specific water deficit responses and will be a resource for future genetic analyses and breeding strategies to develop more drought-tolerant maize cultivars.
format Online
Article
Text
id pubmed-4753846
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-47538462016-02-16 Extensive tissue-specific transcriptomic plasticity in maize primary roots upon water deficit Opitz, Nina Marcon, Caroline Paschold, Anja Malik, Waqas Ahmed Lithio, Andrew Brandt, Ronny Piepho, Hans-Peter Nettleton, Dan Hochholdinger, Frank J Exp Bot Research Paper Water deficit is the most important environmental constraint severely limiting global crop growth and productivity. This study investigated early transcriptome changes in maize (Zea mays L.) primary root tissues in response to moderate water deficit conditions by RNA-Sequencing. Differential gene expression analyses revealed a high degree of plasticity of the water deficit response. The activity status of genes (active/inactive) was determined by a Bayesian hierarchical model. In total, 70% of expressed genes were constitutively active in all tissues. In contrast, <3% (50 genes) of water deficit-responsive genes (1915) were consistently regulated in all tissues, while >75% (1501 genes) were specifically regulated in a single root tissue. Water deficit-responsive genes were most numerous in the cortex of the mature root zone and in the elongation zone. The most prominent functional categories among differentially expressed genes in all tissues were ‘transcriptional regulation’ and ‘hormone metabolism’, indicating global reprogramming of cellular metabolism as an adaptation to water deficit. Additionally, the most significant transcriptomic changes in the root tip were associated with cell wall reorganization, leading to continued root growth despite water deficit conditions. This study provides insight into tissue-specific water deficit responses and will be a resource for future genetic analyses and breeding strategies to develop more drought-tolerant maize cultivars. Oxford University Press 2016-02 2015-10-13 /pmc/articles/PMC4753846/ /pubmed/26463995 http://dx.doi.org/10.1093/jxb/erv453 Text en © The Author 2015. Published by Oxford University Press on behalf of the Society for Experimental Biology. http://creativecommons.org/licenses/by/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Paper
Opitz, Nina
Marcon, Caroline
Paschold, Anja
Malik, Waqas Ahmed
Lithio, Andrew
Brandt, Ronny
Piepho, Hans-Peter
Nettleton, Dan
Hochholdinger, Frank
Extensive tissue-specific transcriptomic plasticity in maize primary roots upon water deficit
title Extensive tissue-specific transcriptomic plasticity in maize primary roots upon water deficit
title_full Extensive tissue-specific transcriptomic plasticity in maize primary roots upon water deficit
title_fullStr Extensive tissue-specific transcriptomic plasticity in maize primary roots upon water deficit
title_full_unstemmed Extensive tissue-specific transcriptomic plasticity in maize primary roots upon water deficit
title_short Extensive tissue-specific transcriptomic plasticity in maize primary roots upon water deficit
title_sort extensive tissue-specific transcriptomic plasticity in maize primary roots upon water deficit
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4753846/
https://www.ncbi.nlm.nih.gov/pubmed/26463995
http://dx.doi.org/10.1093/jxb/erv453
work_keys_str_mv AT opitznina extensivetissuespecifictranscriptomicplasticityinmaizeprimaryrootsuponwaterdeficit
AT marconcaroline extensivetissuespecifictranscriptomicplasticityinmaizeprimaryrootsuponwaterdeficit
AT pascholdanja extensivetissuespecifictranscriptomicplasticityinmaizeprimaryrootsuponwaterdeficit
AT malikwaqasahmed extensivetissuespecifictranscriptomicplasticityinmaizeprimaryrootsuponwaterdeficit
AT lithioandrew extensivetissuespecifictranscriptomicplasticityinmaizeprimaryrootsuponwaterdeficit
AT brandtronny extensivetissuespecifictranscriptomicplasticityinmaizeprimaryrootsuponwaterdeficit
AT piephohanspeter extensivetissuespecifictranscriptomicplasticityinmaizeprimaryrootsuponwaterdeficit
AT nettletondan extensivetissuespecifictranscriptomicplasticityinmaizeprimaryrootsuponwaterdeficit
AT hochholdingerfrank extensivetissuespecifictranscriptomicplasticityinmaizeprimaryrootsuponwaterdeficit