Cargando…
Integrated dominance mechanisms regulate reproductive architecture in Arabidopsis thaliana and Brassica napus
The production of seed in flowering plants is complicated by the need to first invest in reproductive shoots, inflorescences, flowers, and fruit. Furthermore, in many species, it will be months between plants generating flowers and setting seed. How can plants therefore produce an optimal seed-set r...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8331136/ https://www.ncbi.nlm.nih.gov/pubmed/33914872 http://dx.doi.org/10.1093/plphys/kiab194 |
_version_ | 1783732860539109376 |
---|---|
author | Walker, Catriona H Wheeldon, Cara D Bennett, Tom |
author_facet | Walker, Catriona H Wheeldon, Cara D Bennett, Tom |
author_sort | Walker, Catriona H |
collection | PubMed |
description | The production of seed in flowering plants is complicated by the need to first invest in reproductive shoots, inflorescences, flowers, and fruit. Furthermore, in many species, it will be months between plants generating flowers and setting seed. How can plants therefore produce an optimal seed-set relative to environmental resources when the “reproductive architecture” that supports seed-set needs to be elaborated so far in advance? Here, we address this question by investigating the spatio-temporal control of reproductive architecture in Arabidopsis (Arabidopsis thaliana) and Brassica napus. We show that resource and resource-related signals such as substrate volume play a key role in determining the scale of reproductive effort, and that this is reflected in the earliest events in reproductive development, which broadly predict the subsequent reproductive effort. We show that a series of negative feedbacks both within and between developmental stages prevent plants from over-committing to early stages of development. These feedbacks create a highly plastic, homeostatic system in which additional organs can be produced in the case of reproductive failure elsewhere in the system. We propose that these feedbacks represent an “integrated dominance” mechanism that allows resource use to be correctly sequenced between developmental stages to optimize seed set. |
format | Online Article Text |
id | pubmed-8331136 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-83311362021-12-01 Integrated dominance mechanisms regulate reproductive architecture in Arabidopsis thaliana and Brassica napus Walker, Catriona H Wheeldon, Cara D Bennett, Tom Plant Physiol Research Articles The production of seed in flowering plants is complicated by the need to first invest in reproductive shoots, inflorescences, flowers, and fruit. Furthermore, in many species, it will be months between plants generating flowers and setting seed. How can plants therefore produce an optimal seed-set relative to environmental resources when the “reproductive architecture” that supports seed-set needs to be elaborated so far in advance? Here, we address this question by investigating the spatio-temporal control of reproductive architecture in Arabidopsis (Arabidopsis thaliana) and Brassica napus. We show that resource and resource-related signals such as substrate volume play a key role in determining the scale of reproductive effort, and that this is reflected in the earliest events in reproductive development, which broadly predict the subsequent reproductive effort. We show that a series of negative feedbacks both within and between developmental stages prevent plants from over-committing to early stages of development. These feedbacks create a highly plastic, homeostatic system in which additional organs can be produced in the case of reproductive failure elsewhere in the system. We propose that these feedbacks represent an “integrated dominance” mechanism that allows resource use to be correctly sequenced between developmental stages to optimize seed set. Oxford University Press 2021-04-29 /pmc/articles/PMC8331136/ /pubmed/33914872 http://dx.doi.org/10.1093/plphys/kiab194 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of American Society of Plant Biologists. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Walker, Catriona H Wheeldon, Cara D Bennett, Tom Integrated dominance mechanisms regulate reproductive architecture in Arabidopsis thaliana and Brassica napus |
title | Integrated dominance mechanisms regulate reproductive architecture in Arabidopsis thaliana and Brassica napus |
title_full | Integrated dominance mechanisms regulate reproductive architecture in Arabidopsis thaliana and Brassica napus |
title_fullStr | Integrated dominance mechanisms regulate reproductive architecture in Arabidopsis thaliana and Brassica napus |
title_full_unstemmed | Integrated dominance mechanisms regulate reproductive architecture in Arabidopsis thaliana and Brassica napus |
title_short | Integrated dominance mechanisms regulate reproductive architecture in Arabidopsis thaliana and Brassica napus |
title_sort | integrated dominance mechanisms regulate reproductive architecture in arabidopsis thaliana and brassica napus |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8331136/ https://www.ncbi.nlm.nih.gov/pubmed/33914872 http://dx.doi.org/10.1093/plphys/kiab194 |
work_keys_str_mv | AT walkercatrionah integrateddominancemechanismsregulatereproductivearchitectureinarabidopsisthalianaandbrassicanapus AT wheeldoncarad integrateddominancemechanismsregulatereproductivearchitectureinarabidopsisthalianaandbrassicanapus AT bennetttom integrateddominancemechanismsregulatereproductivearchitectureinarabidopsisthalianaandbrassicanapus |