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...
Autores principales: | , , , , , , , |
---|---|
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 |