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Gene expression trajectories during male and female reproductive development in balsam poplar (Populus balsamifera L.)
Plant reproductive development from the first appearance of reproductively committed axes through to floral maturation requires massive and rapid remarshalling of gene expression. In dioecious species such as poplar this is further complicated by divergent male and female developmental programs. We...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7242425/ https://www.ncbi.nlm.nih.gov/pubmed/32439903 http://dx.doi.org/10.1038/s41598-020-64938-w |
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author | Cronk, Quentin Soolanayakanahally, Raju Bräutigam, Katharina |
author_facet | Cronk, Quentin Soolanayakanahally, Raju Bräutigam, Katharina |
author_sort | Cronk, Quentin |
collection | PubMed |
description | Plant reproductive development from the first appearance of reproductively committed axes through to floral maturation requires massive and rapid remarshalling of gene expression. In dioecious species such as poplar this is further complicated by divergent male and female developmental programs. We used seven time points in male and female balsam poplar (Populus balsamifera L.) buds and catkins representing the full annual flowering cycle, to elucidate the effects of time and sex on gene expression during reproductive development. Time (developmental stage) is dominant in patterning gene expression with the effect of sex nested within this. Here, we find (1) evidence for five successive waves of alterations to the chromatin landscape which may be important in setting the overall reproductive trajectory, regardless of sex. (2) Each individual developmental stage is further characterized by marked sex-differential gene expression. (3) Consistent sexually differentiated gene expression regardless of developmental stage reveal candidates for high-level regulators of sex and include the female-specific poplar ARR17 homologue. There is also consistent male-biased expression of the MADS-box genes PISTILLATA and APETALA3. Our work provides insights into expression trajectories shaping reproductive development, its potential underlying mechanisms, and sex-specific translation of the genome information into reproductive structures in balsam poplar. |
format | Online Article Text |
id | pubmed-7242425 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-72424252020-05-30 Gene expression trajectories during male and female reproductive development in balsam poplar (Populus balsamifera L.) Cronk, Quentin Soolanayakanahally, Raju Bräutigam, Katharina Sci Rep Article Plant reproductive development from the first appearance of reproductively committed axes through to floral maturation requires massive and rapid remarshalling of gene expression. In dioecious species such as poplar this is further complicated by divergent male and female developmental programs. We used seven time points in male and female balsam poplar (Populus balsamifera L.) buds and catkins representing the full annual flowering cycle, to elucidate the effects of time and sex on gene expression during reproductive development. Time (developmental stage) is dominant in patterning gene expression with the effect of sex nested within this. Here, we find (1) evidence for five successive waves of alterations to the chromatin landscape which may be important in setting the overall reproductive trajectory, regardless of sex. (2) Each individual developmental stage is further characterized by marked sex-differential gene expression. (3) Consistent sexually differentiated gene expression regardless of developmental stage reveal candidates for high-level regulators of sex and include the female-specific poplar ARR17 homologue. There is also consistent male-biased expression of the MADS-box genes PISTILLATA and APETALA3. Our work provides insights into expression trajectories shaping reproductive development, its potential underlying mechanisms, and sex-specific translation of the genome information into reproductive structures in balsam poplar. Nature Publishing Group UK 2020-05-21 /pmc/articles/PMC7242425/ /pubmed/32439903 http://dx.doi.org/10.1038/s41598-020-64938-w Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Cronk, Quentin Soolanayakanahally, Raju Bräutigam, Katharina Gene expression trajectories during male and female reproductive development in balsam poplar (Populus balsamifera L.) |
title | Gene expression trajectories during male and female reproductive development in balsam poplar (Populus balsamifera L.) |
title_full | Gene expression trajectories during male and female reproductive development in balsam poplar (Populus balsamifera L.) |
title_fullStr | Gene expression trajectories during male and female reproductive development in balsam poplar (Populus balsamifera L.) |
title_full_unstemmed | Gene expression trajectories during male and female reproductive development in balsam poplar (Populus balsamifera L.) |
title_short | Gene expression trajectories during male and female reproductive development in balsam poplar (Populus balsamifera L.) |
title_sort | gene expression trajectories during male and female reproductive development in balsam poplar (populus balsamifera l.) |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7242425/ https://www.ncbi.nlm.nih.gov/pubmed/32439903 http://dx.doi.org/10.1038/s41598-020-64938-w |
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