Cargando…

Digital gene expression analysis of male and female bud transition in Metasequoia reveals high activity of MADS-box transcription factors and hormone-mediated sugar pathways

Metasequoia glyptostroboides is a famous redwood tree of ecological and economic importance, and requires more than 20 years of juvenile-to-adult transition before producing female and male cones. Previously, we induced reproductive buds using a hormone solution in juvenile Metasequoia trees as youn...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhao, Ying, Liang, Haiying, Li, Lan, Tang, Sha, Han, Xiao, Wang, Congpeng, Xia, Xinli, Yin, Weilun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4478380/
https://www.ncbi.nlm.nih.gov/pubmed/26157452
http://dx.doi.org/10.3389/fpls.2015.00467
_version_ 1782377879820042240
author Zhao, Ying
Liang, Haiying
Li, Lan
Tang, Sha
Han, Xiao
Wang, Congpeng
Xia, Xinli
Yin, Weilun
author_facet Zhao, Ying
Liang, Haiying
Li, Lan
Tang, Sha
Han, Xiao
Wang, Congpeng
Xia, Xinli
Yin, Weilun
author_sort Zhao, Ying
collection PubMed
description Metasequoia glyptostroboides is a famous redwood tree of ecological and economic importance, and requires more than 20 years of juvenile-to-adult transition before producing female and male cones. Previously, we induced reproductive buds using a hormone solution in juvenile Metasequoia trees as young as 5-to-7 years old. In the current study, hormone-treated shoots found in female and male buds were used to identify candidate genes involved in reproductive bud transition in Metasequoia. Samples from hormone-treated cone reproductive shoots and naturally occurring non-cone setting shoots were analyzed using 24 digital gene expression (DGE) tag profiles using Illumina, generating a total of 69,520 putative transcripts. Next, 32 differentially and specifically expressed transcripts were determined using quantitative real-time polymerase chain reaction, including the upregulation of MADS-box transcription factors involved in male bud transition and flowering time control proteins involved in female bud transition. These differentially expressed transcripts were associated with 243 KEGG pathways. Among the significantly changed pathways, sugar pathways were mediated by hormone signals during the vegetative-to-reproductive phase transition, including glycolysis/gluconeogenesis and sucrose and starch metabolism pathways. Key enzymes were identified in these pathways, including alcohol dehydrogenase (NAD) and glutathione dehydrogenase for the glycolysis/gluconeogenesis pathway, and glucanphosphorylase for sucrose and starch metabolism pathways. Our results increase our understanding of the reproductive bud transition in gymnosperms. In addition, these studies on hormone-mediated sugar pathways increase our understanding of the relationship between sugar and hormone signaling during female and male bud initiation in Metasequoia.
format Online
Article
Text
id pubmed-4478380
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-44783802015-07-08 Digital gene expression analysis of male and female bud transition in Metasequoia reveals high activity of MADS-box transcription factors and hormone-mediated sugar pathways Zhao, Ying Liang, Haiying Li, Lan Tang, Sha Han, Xiao Wang, Congpeng Xia, Xinli Yin, Weilun Front Plant Sci Plant Science Metasequoia glyptostroboides is a famous redwood tree of ecological and economic importance, and requires more than 20 years of juvenile-to-adult transition before producing female and male cones. Previously, we induced reproductive buds using a hormone solution in juvenile Metasequoia trees as young as 5-to-7 years old. In the current study, hormone-treated shoots found in female and male buds were used to identify candidate genes involved in reproductive bud transition in Metasequoia. Samples from hormone-treated cone reproductive shoots and naturally occurring non-cone setting shoots were analyzed using 24 digital gene expression (DGE) tag profiles using Illumina, generating a total of 69,520 putative transcripts. Next, 32 differentially and specifically expressed transcripts were determined using quantitative real-time polymerase chain reaction, including the upregulation of MADS-box transcription factors involved in male bud transition and flowering time control proteins involved in female bud transition. These differentially expressed transcripts were associated with 243 KEGG pathways. Among the significantly changed pathways, sugar pathways were mediated by hormone signals during the vegetative-to-reproductive phase transition, including glycolysis/gluconeogenesis and sucrose and starch metabolism pathways. Key enzymes were identified in these pathways, including alcohol dehydrogenase (NAD) and glutathione dehydrogenase for the glycolysis/gluconeogenesis pathway, and glucanphosphorylase for sucrose and starch metabolism pathways. Our results increase our understanding of the reproductive bud transition in gymnosperms. In addition, these studies on hormone-mediated sugar pathways increase our understanding of the relationship between sugar and hormone signaling during female and male bud initiation in Metasequoia. Frontiers Media S.A. 2015-06-24 /pmc/articles/PMC4478380/ /pubmed/26157452 http://dx.doi.org/10.3389/fpls.2015.00467 Text en Copyright © 2015 Zhao, Liang, Li, Tang, Han, Wang, Xia and Yin. 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
Zhao, Ying
Liang, Haiying
Li, Lan
Tang, Sha
Han, Xiao
Wang, Congpeng
Xia, Xinli
Yin, Weilun
Digital gene expression analysis of male and female bud transition in Metasequoia reveals high activity of MADS-box transcription factors and hormone-mediated sugar pathways
title Digital gene expression analysis of male and female bud transition in Metasequoia reveals high activity of MADS-box transcription factors and hormone-mediated sugar pathways
title_full Digital gene expression analysis of male and female bud transition in Metasequoia reveals high activity of MADS-box transcription factors and hormone-mediated sugar pathways
title_fullStr Digital gene expression analysis of male and female bud transition in Metasequoia reveals high activity of MADS-box transcription factors and hormone-mediated sugar pathways
title_full_unstemmed Digital gene expression analysis of male and female bud transition in Metasequoia reveals high activity of MADS-box transcription factors and hormone-mediated sugar pathways
title_short Digital gene expression analysis of male and female bud transition in Metasequoia reveals high activity of MADS-box transcription factors and hormone-mediated sugar pathways
title_sort digital gene expression analysis of male and female bud transition in metasequoia reveals high activity of mads-box transcription factors and hormone-mediated sugar pathways
topic Plant Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4478380/
https://www.ncbi.nlm.nih.gov/pubmed/26157452
http://dx.doi.org/10.3389/fpls.2015.00467
work_keys_str_mv AT zhaoying digitalgeneexpressionanalysisofmaleandfemalebudtransitioninmetasequoiarevealshighactivityofmadsboxtranscriptionfactorsandhormonemediatedsugarpathways
AT lianghaiying digitalgeneexpressionanalysisofmaleandfemalebudtransitioninmetasequoiarevealshighactivityofmadsboxtranscriptionfactorsandhormonemediatedsugarpathways
AT lilan digitalgeneexpressionanalysisofmaleandfemalebudtransitioninmetasequoiarevealshighactivityofmadsboxtranscriptionfactorsandhormonemediatedsugarpathways
AT tangsha digitalgeneexpressionanalysisofmaleandfemalebudtransitioninmetasequoiarevealshighactivityofmadsboxtranscriptionfactorsandhormonemediatedsugarpathways
AT hanxiao digitalgeneexpressionanalysisofmaleandfemalebudtransitioninmetasequoiarevealshighactivityofmadsboxtranscriptionfactorsandhormonemediatedsugarpathways
AT wangcongpeng digitalgeneexpressionanalysisofmaleandfemalebudtransitioninmetasequoiarevealshighactivityofmadsboxtranscriptionfactorsandhormonemediatedsugarpathways
AT xiaxinli digitalgeneexpressionanalysisofmaleandfemalebudtransitioninmetasequoiarevealshighactivityofmadsboxtranscriptionfactorsandhormonemediatedsugarpathways
AT yinweilun digitalgeneexpressionanalysisofmaleandfemalebudtransitioninmetasequoiarevealshighactivityofmadsboxtranscriptionfactorsandhormonemediatedsugarpathways