Cargando…

Using Transcriptomics to Identify Differential Gene Expression in Response to Salinity among Australian Phragmites australis Clones

Common Reed (Phragmites australis) is a frequent component of inland and coastal wetlands in temperate zones worldwide. Ongoing environmental changes have resulted in the decline of this species in many areas and invasive expansion in others. In the Gippsland Lakes coastal waterway system in south-e...

Descripción completa

Detalles Bibliográficos
Autores principales: Holmes, Gareth D., Hall, Nathan E., Gendall, Anthony R., Boon, Paul I., James, Elizabeth A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4829608/
https://www.ncbi.nlm.nih.gov/pubmed/27148279
http://dx.doi.org/10.3389/fpls.2016.00432
_version_ 1782426769679187968
author Holmes, Gareth D.
Hall, Nathan E.
Gendall, Anthony R.
Boon, Paul I.
James, Elizabeth A.
author_facet Holmes, Gareth D.
Hall, Nathan E.
Gendall, Anthony R.
Boon, Paul I.
James, Elizabeth A.
author_sort Holmes, Gareth D.
collection PubMed
description Common Reed (Phragmites australis) is a frequent component of inland and coastal wetlands in temperate zones worldwide. Ongoing environmental changes have resulted in the decline of this species in many areas and invasive expansion in others. In the Gippsland Lakes coastal waterway system in south-eastern Australia, increasing salinity is thought to have contributed to the loss of fringing P. australis reed beds leading to increased shoreline erosion. A major goal of restoration in this waterway is to address the effect of salinity by planting a genetically diverse range of salt-tolerant P. australis plants. This has prompted an interest in examining the variation in salinity tolerance among clones and the underlying basis of this variation. Transcriptomics is an approach for identifying variation in genes and their expression levels associated with the exposure of plants to environmental stressors. In this paper we present initial results of the first comparative culm transcriptome analysis of P. australis clones. After sampling plants from sites of varied surface water salinity across the Gippsland Lakes, replicates from three clones from highly saline sites (>18 g L(-1) TDS) and three from low salinity sites (<6 g L(-1)) were grown in containers irrigated with either fresh (<0.1 g L(-1)) or saline water (16 g L(-1)). An RNA-Seq protocol was used to generate sequence data from culm tissues from the 12 samples allowing an analysis of differential gene expression. Among the key findings, we identified several genes uniquely up- or down-regulated in clones from highly saline sites when irrigated with saline water relative to clones from low salinity sites. These included the higher relative expression levels of genes associated with photosynthesis and lignan biosynthesis indicative of a greater ability of these clones to maintain growth under saline conditions. Combined with growth data from a parallel study, our data suggests local adaptation of certain clones to salinity and provides a basis for more detailed studies.
format Online
Article
Text
id pubmed-4829608
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-48296082016-05-04 Using Transcriptomics to Identify Differential Gene Expression in Response to Salinity among Australian Phragmites australis Clones Holmes, Gareth D. Hall, Nathan E. Gendall, Anthony R. Boon, Paul I. James, Elizabeth A. Front Plant Sci Plant Science Common Reed (Phragmites australis) is a frequent component of inland and coastal wetlands in temperate zones worldwide. Ongoing environmental changes have resulted in the decline of this species in many areas and invasive expansion in others. In the Gippsland Lakes coastal waterway system in south-eastern Australia, increasing salinity is thought to have contributed to the loss of fringing P. australis reed beds leading to increased shoreline erosion. A major goal of restoration in this waterway is to address the effect of salinity by planting a genetically diverse range of salt-tolerant P. australis plants. This has prompted an interest in examining the variation in salinity tolerance among clones and the underlying basis of this variation. Transcriptomics is an approach for identifying variation in genes and their expression levels associated with the exposure of plants to environmental stressors. In this paper we present initial results of the first comparative culm transcriptome analysis of P. australis clones. After sampling plants from sites of varied surface water salinity across the Gippsland Lakes, replicates from three clones from highly saline sites (>18 g L(-1) TDS) and three from low salinity sites (<6 g L(-1)) were grown in containers irrigated with either fresh (<0.1 g L(-1)) or saline water (16 g L(-1)). An RNA-Seq protocol was used to generate sequence data from culm tissues from the 12 samples allowing an analysis of differential gene expression. Among the key findings, we identified several genes uniquely up- or down-regulated in clones from highly saline sites when irrigated with saline water relative to clones from low salinity sites. These included the higher relative expression levels of genes associated with photosynthesis and lignan biosynthesis indicative of a greater ability of these clones to maintain growth under saline conditions. Combined with growth data from a parallel study, our data suggests local adaptation of certain clones to salinity and provides a basis for more detailed studies. Frontiers Media S.A. 2016-04-13 /pmc/articles/PMC4829608/ /pubmed/27148279 http://dx.doi.org/10.3389/fpls.2016.00432 Text en Copyright © 2016 Holmes, Hall, Gendall, Boon and James. 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) or licensor 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
Holmes, Gareth D.
Hall, Nathan E.
Gendall, Anthony R.
Boon, Paul I.
James, Elizabeth A.
Using Transcriptomics to Identify Differential Gene Expression in Response to Salinity among Australian Phragmites australis Clones
title Using Transcriptomics to Identify Differential Gene Expression in Response to Salinity among Australian Phragmites australis Clones
title_full Using Transcriptomics to Identify Differential Gene Expression in Response to Salinity among Australian Phragmites australis Clones
title_fullStr Using Transcriptomics to Identify Differential Gene Expression in Response to Salinity among Australian Phragmites australis Clones
title_full_unstemmed Using Transcriptomics to Identify Differential Gene Expression in Response to Salinity among Australian Phragmites australis Clones
title_short Using Transcriptomics to Identify Differential Gene Expression in Response to Salinity among Australian Phragmites australis Clones
title_sort using transcriptomics to identify differential gene expression in response to salinity among australian phragmites australis clones
topic Plant Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4829608/
https://www.ncbi.nlm.nih.gov/pubmed/27148279
http://dx.doi.org/10.3389/fpls.2016.00432
work_keys_str_mv AT holmesgarethd usingtranscriptomicstoidentifydifferentialgeneexpressioninresponsetosalinityamongaustralianphragmitesaustralisclones
AT hallnathane usingtranscriptomicstoidentifydifferentialgeneexpressioninresponsetosalinityamongaustralianphragmitesaustralisclones
AT gendallanthonyr usingtranscriptomicstoidentifydifferentialgeneexpressioninresponsetosalinityamongaustralianphragmitesaustralisclones
AT boonpauli usingtranscriptomicstoidentifydifferentialgeneexpressioninresponsetosalinityamongaustralianphragmitesaustralisclones
AT jameselizabetha usingtranscriptomicstoidentifydifferentialgeneexpressioninresponsetosalinityamongaustralianphragmitesaustralisclones