Cargando…
Gene expression and proteomic analysis of shoot apical meristem transition from dormancy to activation in Cunninghamia lanceolata (Lamb.) Hook
In contrast to annual plants, in perennial plants, the shoot apical meristem (SAM) can undergo seasonal transitions between dormancy and activity; understanding this transition is crucial for understanding growth in perennial plants. However, little is known about the molecular mechanisms of SAM dev...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4735791/ https://www.ncbi.nlm.nih.gov/pubmed/26832850 http://dx.doi.org/10.1038/srep19938 |
_version_ | 1782413145753518080 |
---|---|
author | Xu, Huimin Cao, Dechang Chen, Yanmei Wei, Dongmei Wang, Yanwei Stevenson, Rebecca Ann Zhu, Yingfang Lin, Jinxing |
author_facet | Xu, Huimin Cao, Dechang Chen, Yanmei Wei, Dongmei Wang, Yanwei Stevenson, Rebecca Ann Zhu, Yingfang Lin, Jinxing |
author_sort | Xu, Huimin |
collection | PubMed |
description | In contrast to annual plants, in perennial plants, the shoot apical meristem (SAM) can undergo seasonal transitions between dormancy and activity; understanding this transition is crucial for understanding growth in perennial plants. However, little is known about the molecular mechanisms of SAM development in trees. Here, light and transmission electron microscopy revealed that evident changes in starch granules, lipid bodies, and cell walls thickness of the SAM in C. lanceolata during the transition from dormancy to activation. HPLC-ESI-MS/MS analysis showed that levels of indole-3-acetic acid (IAA) increased and levels of abscisic acid (ABA) decreased from dormant to active stage. Examination of 20 genes and 132 differentially expressed proteins revealed that the expression of genes and proteins potentially involved in cell division and expansion significantly increased in the active stage, whereas those related to the abscisic acid insensitive 3(ABI3), the cytoskeleton and energy metabolism decreased in the dormant stage. These findings provide new insights into the complex mechanism of gene and protein expression and their relation to cytological and physiological changes of SAM in this coniferous species. |
format | Online Article Text |
id | pubmed-4735791 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-47357912016-02-05 Gene expression and proteomic analysis of shoot apical meristem transition from dormancy to activation in Cunninghamia lanceolata (Lamb.) Hook Xu, Huimin Cao, Dechang Chen, Yanmei Wei, Dongmei Wang, Yanwei Stevenson, Rebecca Ann Zhu, Yingfang Lin, Jinxing Sci Rep Article In contrast to annual plants, in perennial plants, the shoot apical meristem (SAM) can undergo seasonal transitions between dormancy and activity; understanding this transition is crucial for understanding growth in perennial plants. However, little is known about the molecular mechanisms of SAM development in trees. Here, light and transmission electron microscopy revealed that evident changes in starch granules, lipid bodies, and cell walls thickness of the SAM in C. lanceolata during the transition from dormancy to activation. HPLC-ESI-MS/MS analysis showed that levels of indole-3-acetic acid (IAA) increased and levels of abscisic acid (ABA) decreased from dormant to active stage. Examination of 20 genes and 132 differentially expressed proteins revealed that the expression of genes and proteins potentially involved in cell division and expansion significantly increased in the active stage, whereas those related to the abscisic acid insensitive 3(ABI3), the cytoskeleton and energy metabolism decreased in the dormant stage. These findings provide new insights into the complex mechanism of gene and protein expression and their relation to cytological and physiological changes of SAM in this coniferous species. Nature Publishing Group 2016-02-02 /pmc/articles/PMC4735791/ /pubmed/26832850 http://dx.doi.org/10.1038/srep19938 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Xu, Huimin Cao, Dechang Chen, Yanmei Wei, Dongmei Wang, Yanwei Stevenson, Rebecca Ann Zhu, Yingfang Lin, Jinxing Gene expression and proteomic analysis of shoot apical meristem transition from dormancy to activation in Cunninghamia lanceolata (Lamb.) Hook |
title | Gene expression and proteomic analysis of shoot apical meristem transition from dormancy to activation in Cunninghamia lanceolata (Lamb.) Hook |
title_full | Gene expression and proteomic analysis of shoot apical meristem transition from dormancy to activation in Cunninghamia lanceolata (Lamb.) Hook |
title_fullStr | Gene expression and proteomic analysis of shoot apical meristem transition from dormancy to activation in Cunninghamia lanceolata (Lamb.) Hook |
title_full_unstemmed | Gene expression and proteomic analysis of shoot apical meristem transition from dormancy to activation in Cunninghamia lanceolata (Lamb.) Hook |
title_short | Gene expression and proteomic analysis of shoot apical meristem transition from dormancy to activation in Cunninghamia lanceolata (Lamb.) Hook |
title_sort | gene expression and proteomic analysis of shoot apical meristem transition from dormancy to activation in cunninghamia lanceolata (lamb.) hook |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4735791/ https://www.ncbi.nlm.nih.gov/pubmed/26832850 http://dx.doi.org/10.1038/srep19938 |
work_keys_str_mv | AT xuhuimin geneexpressionandproteomicanalysisofshootapicalmeristemtransitionfromdormancytoactivationincunninghamialanceolatalambhook AT caodechang geneexpressionandproteomicanalysisofshootapicalmeristemtransitionfromdormancytoactivationincunninghamialanceolatalambhook AT chenyanmei geneexpressionandproteomicanalysisofshootapicalmeristemtransitionfromdormancytoactivationincunninghamialanceolatalambhook AT weidongmei geneexpressionandproteomicanalysisofshootapicalmeristemtransitionfromdormancytoactivationincunninghamialanceolatalambhook AT wangyanwei geneexpressionandproteomicanalysisofshootapicalmeristemtransitionfromdormancytoactivationincunninghamialanceolatalambhook AT stevensonrebeccaann geneexpressionandproteomicanalysisofshootapicalmeristemtransitionfromdormancytoactivationincunninghamialanceolatalambhook AT zhuyingfang geneexpressionandproteomicanalysisofshootapicalmeristemtransitionfromdormancytoactivationincunninghamialanceolatalambhook AT linjinxing geneexpressionandproteomicanalysisofshootapicalmeristemtransitionfromdormancytoactivationincunninghamialanceolatalambhook |