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RNA-Seq transcriptome analysis of Spirodela dormancy without reproduction

BACKGROUND: Higher plants exhibit a remarkable phenotypic plasticity to adapt to adverse environmental changes. The Greater Duckweed Spirodela, as an aquatic plant, presents exceptional tolerance to cold winters through its dormant structure of turions in place of seeds. Abundant starch in turions p...

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Autores principales: Wang, Wenqin, Wu, Yongrui, Messing, Joachim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3933069/
https://www.ncbi.nlm.nih.gov/pubmed/24456086
http://dx.doi.org/10.1186/1471-2164-15-60
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author Wang, Wenqin
Wu, Yongrui
Messing, Joachim
author_facet Wang, Wenqin
Wu, Yongrui
Messing, Joachim
author_sort Wang, Wenqin
collection PubMed
description BACKGROUND: Higher plants exhibit a remarkable phenotypic plasticity to adapt to adverse environmental changes. The Greater Duckweed Spirodela, as an aquatic plant, presents exceptional tolerance to cold winters through its dormant structure of turions in place of seeds. Abundant starch in turions permits them to sink and escape the freezing surface of waters. Due to their clonal propagation, they are the fastest growing biomass on earth, providing yet an untapped source for industrial applications. RESULTS: We used next generation sequencing technology to examine the transcriptome of turion development triggered by exogenous ABA. A total of 208 genes showed more than a 4-fold increase compared with 154 down-regulated genes in developing turions. The analysis of up-regulated differential expressed genes in response to dormancy exposed an enriched interplay among various pathways: signal transduction, seed dehydration, carbohydrate and secondary metabolism, and senescence. On the other side, the genes responsible for rapid growth and biomass accumulation through DNA assembly, protein synthesis and carbon fixation are repressed. Noticeably, three members of late embryogenesis abundant protein family are exclusively expressed during turion formation. High expression level of key genes in starch synthesis are APS1, APL3 and GBSSI, which could artificially be reduced for re-directing carbon flow from photosynthesis to create a higher energy biomass. CONCLUSIONS: The identification and functional annotation of differentially expressed genes open a major step towards understanding the molecular network underlying vegetative frond dormancy. Moreover, genes have been identified that could be engineered in duckweeds for practical applications easing agricultural production of food crops.
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spelling pubmed-39330692014-02-25 RNA-Seq transcriptome analysis of Spirodela dormancy without reproduction Wang, Wenqin Wu, Yongrui Messing, Joachim BMC Genomics Research Article BACKGROUND: Higher plants exhibit a remarkable phenotypic plasticity to adapt to adverse environmental changes. The Greater Duckweed Spirodela, as an aquatic plant, presents exceptional tolerance to cold winters through its dormant structure of turions in place of seeds. Abundant starch in turions permits them to sink and escape the freezing surface of waters. Due to their clonal propagation, they are the fastest growing biomass on earth, providing yet an untapped source for industrial applications. RESULTS: We used next generation sequencing technology to examine the transcriptome of turion development triggered by exogenous ABA. A total of 208 genes showed more than a 4-fold increase compared with 154 down-regulated genes in developing turions. The analysis of up-regulated differential expressed genes in response to dormancy exposed an enriched interplay among various pathways: signal transduction, seed dehydration, carbohydrate and secondary metabolism, and senescence. On the other side, the genes responsible for rapid growth and biomass accumulation through DNA assembly, protein synthesis and carbon fixation are repressed. Noticeably, three members of late embryogenesis abundant protein family are exclusively expressed during turion formation. High expression level of key genes in starch synthesis are APS1, APL3 and GBSSI, which could artificially be reduced for re-directing carbon flow from photosynthesis to create a higher energy biomass. CONCLUSIONS: The identification and functional annotation of differentially expressed genes open a major step towards understanding the molecular network underlying vegetative frond dormancy. Moreover, genes have been identified that could be engineered in duckweeds for practical applications easing agricultural production of food crops. BioMed Central 2014-01-23 /pmc/articles/PMC3933069/ /pubmed/24456086 http://dx.doi.org/10.1186/1471-2164-15-60 Text en Copyright © 2014 Wang et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. 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
Wang, Wenqin
Wu, Yongrui
Messing, Joachim
RNA-Seq transcriptome analysis of Spirodela dormancy without reproduction
title RNA-Seq transcriptome analysis of Spirodela dormancy without reproduction
title_full RNA-Seq transcriptome analysis of Spirodela dormancy without reproduction
title_fullStr RNA-Seq transcriptome analysis of Spirodela dormancy without reproduction
title_full_unstemmed RNA-Seq transcriptome analysis of Spirodela dormancy without reproduction
title_short RNA-Seq transcriptome analysis of Spirodela dormancy without reproduction
title_sort rna-seq transcriptome analysis of spirodela dormancy without reproduction
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3933069/
https://www.ncbi.nlm.nih.gov/pubmed/24456086
http://dx.doi.org/10.1186/1471-2164-15-60
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