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Extensive Transcriptome Changes During Natural Onset and Release of Vegetative Bud Dormancy in Populus

To survive winter, many perennial plants become endodormant, a state of suspended growth maintained even in favorable growing environments. To understand vegetative bud endodormancy, we collected paradormant, endodormant, and ecodormant axillary buds from Populus trees growing under natural conditio...

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Autores principales: Howe, Glenn T., Horvath, David P., Dharmawardhana, Palitha, Priest, Henry D., Mockler, Todd C., Strauss, Steven H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4681841/
https://www.ncbi.nlm.nih.gov/pubmed/26734012
http://dx.doi.org/10.3389/fpls.2015.00989
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author Howe, Glenn T.
Horvath, David P.
Dharmawardhana, Palitha
Priest, Henry D.
Mockler, Todd C.
Strauss, Steven H.
author_facet Howe, Glenn T.
Horvath, David P.
Dharmawardhana, Palitha
Priest, Henry D.
Mockler, Todd C.
Strauss, Steven H.
author_sort Howe, Glenn T.
collection PubMed
description To survive winter, many perennial plants become endodormant, a state of suspended growth maintained even in favorable growing environments. To understand vegetative bud endodormancy, we collected paradormant, endodormant, and ecodormant axillary buds from Populus trees growing under natural conditions. Of 44,441 Populus gene models analyzed using NimbleGen microarrays, we found that 1,362 (3.1%) were differentially expressed among the three dormancy states, and 429 (1.0%) were differentially expressed during only one of the two dormancy transitions (FDR p-value < 0.05). Of all differentially expressed genes, 69% were down-regulated from paradormancy to endodormancy, which was expected given the lower metabolic activity associated with endodormancy. Dormancy transitions were accompanied by changes in genes associated with DNA methylation (via RNA-directed DNA methylation) and histone modifications (via Polycomb Repressive Complex 2), confirming and extending knowledge of chromatin modifications as major features of dormancy transitions. Among the chromatin-associated genes, two genes similar to SPT (SUPPRESSOR OF TY) were strongly up-regulated during endodormancy. Transcription factor genes and gene sets that were atypically up-regulated during endodormancy include a gene that seems to encode a trihelix transcription factor and genes associated with proteins involved in responses to ethylene, cold, and other abiotic stresses. These latter transcription factors include ETHYLENE INSENSITIVE 3 (EIN3), ETHYLENE-RESPONSIVE ELEMENT BINDING PROTEIN (EBP), ETHYLENE RESPONSE FACTOR (ERF), ZINC FINGER PROTEIN 10 (ZAT10), ZAT12, and WRKY DNA-binding domain proteins. Analyses of phytohormone-associated genes suggest important changes in responses to ethylene, auxin, and brassinosteroids occur during endodormancy. We found weaker evidence for changes in genes associated with salicylic acid and jasmonic acid, and little evidence for important changes in genes associated with gibberellins, abscisic acid, and cytokinin. We identified 315 upstream sequence motifs associated with eight patterns of gene expression, including novel motifs and motifs associated with the circadian clock and responses to photoperiod, cold, dehydration, and ABA. Analogies between flowering and endodormancy suggest important roles for genes similar to SQUAMOSA-PROMOTER BINDING PROTEIN-LIKE (SPL), DORMANCY ASSOCIATED MADS-BOX (DAM), and SUPPRESSOR OF OVEREXPRESSION OF CONSTANS 1 (SOC1).
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spelling pubmed-46818412016-01-05 Extensive Transcriptome Changes During Natural Onset and Release of Vegetative Bud Dormancy in Populus Howe, Glenn T. Horvath, David P. Dharmawardhana, Palitha Priest, Henry D. Mockler, Todd C. Strauss, Steven H. Front Plant Sci Plant Science To survive winter, many perennial plants become endodormant, a state of suspended growth maintained even in favorable growing environments. To understand vegetative bud endodormancy, we collected paradormant, endodormant, and ecodormant axillary buds from Populus trees growing under natural conditions. Of 44,441 Populus gene models analyzed using NimbleGen microarrays, we found that 1,362 (3.1%) were differentially expressed among the three dormancy states, and 429 (1.0%) were differentially expressed during only one of the two dormancy transitions (FDR p-value < 0.05). Of all differentially expressed genes, 69% were down-regulated from paradormancy to endodormancy, which was expected given the lower metabolic activity associated with endodormancy. Dormancy transitions were accompanied by changes in genes associated with DNA methylation (via RNA-directed DNA methylation) and histone modifications (via Polycomb Repressive Complex 2), confirming and extending knowledge of chromatin modifications as major features of dormancy transitions. Among the chromatin-associated genes, two genes similar to SPT (SUPPRESSOR OF TY) were strongly up-regulated during endodormancy. Transcription factor genes and gene sets that were atypically up-regulated during endodormancy include a gene that seems to encode a trihelix transcription factor and genes associated with proteins involved in responses to ethylene, cold, and other abiotic stresses. These latter transcription factors include ETHYLENE INSENSITIVE 3 (EIN3), ETHYLENE-RESPONSIVE ELEMENT BINDING PROTEIN (EBP), ETHYLENE RESPONSE FACTOR (ERF), ZINC FINGER PROTEIN 10 (ZAT10), ZAT12, and WRKY DNA-binding domain proteins. Analyses of phytohormone-associated genes suggest important changes in responses to ethylene, auxin, and brassinosteroids occur during endodormancy. We found weaker evidence for changes in genes associated with salicylic acid and jasmonic acid, and little evidence for important changes in genes associated with gibberellins, abscisic acid, and cytokinin. We identified 315 upstream sequence motifs associated with eight patterns of gene expression, including novel motifs and motifs associated with the circadian clock and responses to photoperiod, cold, dehydration, and ABA. Analogies between flowering and endodormancy suggest important roles for genes similar to SQUAMOSA-PROMOTER BINDING PROTEIN-LIKE (SPL), DORMANCY ASSOCIATED MADS-BOX (DAM), and SUPPRESSOR OF OVEREXPRESSION OF CONSTANS 1 (SOC1). Frontiers Media S.A. 2015-12-17 /pmc/articles/PMC4681841/ /pubmed/26734012 http://dx.doi.org/10.3389/fpls.2015.00989 Text en Copyright © 2015 Howe, Horvath, Dharmawardhana, Priest, Mockler and Strauss. 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
Howe, Glenn T.
Horvath, David P.
Dharmawardhana, Palitha
Priest, Henry D.
Mockler, Todd C.
Strauss, Steven H.
Extensive Transcriptome Changes During Natural Onset and Release of Vegetative Bud Dormancy in Populus
title Extensive Transcriptome Changes During Natural Onset and Release of Vegetative Bud Dormancy in Populus
title_full Extensive Transcriptome Changes During Natural Onset and Release of Vegetative Bud Dormancy in Populus
title_fullStr Extensive Transcriptome Changes During Natural Onset and Release of Vegetative Bud Dormancy in Populus
title_full_unstemmed Extensive Transcriptome Changes During Natural Onset and Release of Vegetative Bud Dormancy in Populus
title_short Extensive Transcriptome Changes During Natural Onset and Release of Vegetative Bud Dormancy in Populus
title_sort extensive transcriptome changes during natural onset and release of vegetative bud dormancy in populus
topic Plant Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4681841/
https://www.ncbi.nlm.nih.gov/pubmed/26734012
http://dx.doi.org/10.3389/fpls.2015.00989
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