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Shared and genetically distinct Zea mays transcriptome responses to ongoing and past low temperature exposure

BACKGROUND: Cold temperatures and their alleviation affect many plant traits including the abundance of protein coding gene transcripts. Transcript level changes that occur in response to cold temperatures and their alleviation are shared or vary across genotypes. In this study we identify individua...

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Autores principales: Avila, Luis M, Obeidat, Wisam, Earl, Hugh, Niu, Xiaomu, Hargreaves, William, Lukens, Lewis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6196024/
https://www.ncbi.nlm.nih.gov/pubmed/30342485
http://dx.doi.org/10.1186/s12864-018-5134-7
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author Avila, Luis M
Obeidat, Wisam
Earl, Hugh
Niu, Xiaomu
Hargreaves, William
Lukens, Lewis
author_facet Avila, Luis M
Obeidat, Wisam
Earl, Hugh
Niu, Xiaomu
Hargreaves, William
Lukens, Lewis
author_sort Avila, Luis M
collection PubMed
description BACKGROUND: Cold temperatures and their alleviation affect many plant traits including the abundance of protein coding gene transcripts. Transcript level changes that occur in response to cold temperatures and their alleviation are shared or vary across genotypes. In this study we identify individual transcripts and groups of functionally related transcripts that consistently respond to cold and its alleviation. Genes that respond differently to temperature changes across genotypes may have limited functional importance. We investigate if these genes share functions, and if their genotype-specific gene expression levels change in magnitude or rank across temperatures. RESULTS: We estimate transcript abundances from over 22,000 genes in two unrelated Zea mays inbred lines during and after cold temperature exposure. Genotype and temperature contribute to many genes’ abundances. Past cold exposure affects many fewer genes. Genes up-regulated in cold encode many cytokinin glucoside biosynthesis enzymes, transcription factors, signalling molecules, and proteins involved in diverse environmental responses. After cold exposure, protease inhibitors and cuticular wax genes are newly up-regulated, and environmentally responsive genes continue to be up-regulated. Genes down-regulated in response to cold include many photosynthesis, translation, and DNA replication associated genes. After cold exposure, DNA replication and translation genes are still preferentially downregulated. Lignin and suberin biosynthesis are newly down-regulated. DNA replication, reactive oxygen species response, and anthocyanin biosynthesis genes have strong, genotype-specific temperature responses. The ranks of genotypes’ transcript abundances often change across temperatures. CONCLUSIONS: We report a large, core transcriptome response to cold and the alleviation of cold. In cold, many of the core suite of genes are up or downregulated to control plant growth and photosynthesis and limit cellular damage. In recovery, core responses are in part to prepare for future stress. Functionally related genes are consistently and greatly up-regulated in a single genotype in response to cold or its alleviation, suggesting positive selection has driven genotype-specific temperature responses in maize. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12864-018-5134-7) contains supplementary material, which is available to authorized users.
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spelling pubmed-61960242018-10-30 Shared and genetically distinct Zea mays transcriptome responses to ongoing and past low temperature exposure Avila, Luis M Obeidat, Wisam Earl, Hugh Niu, Xiaomu Hargreaves, William Lukens, Lewis BMC Genomics Research Article BACKGROUND: Cold temperatures and their alleviation affect many plant traits including the abundance of protein coding gene transcripts. Transcript level changes that occur in response to cold temperatures and their alleviation are shared or vary across genotypes. In this study we identify individual transcripts and groups of functionally related transcripts that consistently respond to cold and its alleviation. Genes that respond differently to temperature changes across genotypes may have limited functional importance. We investigate if these genes share functions, and if their genotype-specific gene expression levels change in magnitude or rank across temperatures. RESULTS: We estimate transcript abundances from over 22,000 genes in two unrelated Zea mays inbred lines during and after cold temperature exposure. Genotype and temperature contribute to many genes’ abundances. Past cold exposure affects many fewer genes. Genes up-regulated in cold encode many cytokinin glucoside biosynthesis enzymes, transcription factors, signalling molecules, and proteins involved in diverse environmental responses. After cold exposure, protease inhibitors and cuticular wax genes are newly up-regulated, and environmentally responsive genes continue to be up-regulated. Genes down-regulated in response to cold include many photosynthesis, translation, and DNA replication associated genes. After cold exposure, DNA replication and translation genes are still preferentially downregulated. Lignin and suberin biosynthesis are newly down-regulated. DNA replication, reactive oxygen species response, and anthocyanin biosynthesis genes have strong, genotype-specific temperature responses. The ranks of genotypes’ transcript abundances often change across temperatures. CONCLUSIONS: We report a large, core transcriptome response to cold and the alleviation of cold. In cold, many of the core suite of genes are up or downregulated to control plant growth and photosynthesis and limit cellular damage. In recovery, core responses are in part to prepare for future stress. Functionally related genes are consistently and greatly up-regulated in a single genotype in response to cold or its alleviation, suggesting positive selection has driven genotype-specific temperature responses in maize. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12864-018-5134-7) contains supplementary material, which is available to authorized users. BioMed Central 2018-10-20 /pmc/articles/PMC6196024/ /pubmed/30342485 http://dx.doi.org/10.1186/s12864-018-5134-7 Text en © The Author(s). 2018 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Avila, Luis M
Obeidat, Wisam
Earl, Hugh
Niu, Xiaomu
Hargreaves, William
Lukens, Lewis
Shared and genetically distinct Zea mays transcriptome responses to ongoing and past low temperature exposure
title Shared and genetically distinct Zea mays transcriptome responses to ongoing and past low temperature exposure
title_full Shared and genetically distinct Zea mays transcriptome responses to ongoing and past low temperature exposure
title_fullStr Shared and genetically distinct Zea mays transcriptome responses to ongoing and past low temperature exposure
title_full_unstemmed Shared and genetically distinct Zea mays transcriptome responses to ongoing and past low temperature exposure
title_short Shared and genetically distinct Zea mays transcriptome responses to ongoing and past low temperature exposure
title_sort shared and genetically distinct zea mays transcriptome responses to ongoing and past low temperature exposure
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6196024/
https://www.ncbi.nlm.nih.gov/pubmed/30342485
http://dx.doi.org/10.1186/s12864-018-5134-7
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