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Changing the spatial pattern of TFL1 expression reveals its key role in the shoot meristem in controlling Arabidopsis flowering architecture

Models for the control of above-ground plant architectures show how meristems can be programmed to be either shoots or flowers. Molecular, genetic, transgenic, and mathematical studies have greatly refined these models, suggesting that the phase of the shoot reflects different genes contributing to...

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Autores principales: Baumann, Kim, Venail, Julien, Berbel, Ana, Domenech, Maria Jose, Money, Tracy, Conti, Lucio, Hanzawa, Yoshie, Madueno, Francisco, Bradley, Desmond
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4507777/
https://www.ncbi.nlm.nih.gov/pubmed/26019254
http://dx.doi.org/10.1093/jxb/erv247
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author Baumann, Kim
Venail, Julien
Berbel, Ana
Domenech, Maria Jose
Money, Tracy
Conti, Lucio
Hanzawa, Yoshie
Madueno, Francisco
Bradley, Desmond
author_facet Baumann, Kim
Venail, Julien
Berbel, Ana
Domenech, Maria Jose
Money, Tracy
Conti, Lucio
Hanzawa, Yoshie
Madueno, Francisco
Bradley, Desmond
author_sort Baumann, Kim
collection PubMed
description Models for the control of above-ground plant architectures show how meristems can be programmed to be either shoots or flowers. Molecular, genetic, transgenic, and mathematical studies have greatly refined these models, suggesting that the phase of the shoot reflects different genes contributing to its repression of flowering, its vegetativeness (‘veg’), before activators promote flower development. Key elements of how the repressor of flowering and shoot meristem gene TFL1 acts have now been tested, by changing its spatiotemporal pattern. It is shown that TFL1 can act outside of its normal expression domain in leaf primordia or floral meristems to repress flower identity. These data show how the timing and spatial pattern of TFL1 expression affect overall plant architecture. This reveals that the underlying pattern of TFL1 interactors is complex and that they may be spatially more widespread than TFL1 itself, which is confined to shoots. However, the data show that while TFL1 and floral genes can both act and compete in the same meristem, it appears that the main shoot meristem is more sensitive to TFL1 rather than floral genes. This spatial analysis therefore reveals how a difference in response helps maintain the ‘veg’ state of the shoot meristem.
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spelling pubmed-45077772015-07-22 Changing the spatial pattern of TFL1 expression reveals its key role in the shoot meristem in controlling Arabidopsis flowering architecture Baumann, Kim Venail, Julien Berbel, Ana Domenech, Maria Jose Money, Tracy Conti, Lucio Hanzawa, Yoshie Madueno, Francisco Bradley, Desmond J Exp Bot Research Paper Models for the control of above-ground plant architectures show how meristems can be programmed to be either shoots or flowers. Molecular, genetic, transgenic, and mathematical studies have greatly refined these models, suggesting that the phase of the shoot reflects different genes contributing to its repression of flowering, its vegetativeness (‘veg’), before activators promote flower development. Key elements of how the repressor of flowering and shoot meristem gene TFL1 acts have now been tested, by changing its spatiotemporal pattern. It is shown that TFL1 can act outside of its normal expression domain in leaf primordia or floral meristems to repress flower identity. These data show how the timing and spatial pattern of TFL1 expression affect overall plant architecture. This reveals that the underlying pattern of TFL1 interactors is complex and that they may be spatially more widespread than TFL1 itself, which is confined to shoots. However, the data show that while TFL1 and floral genes can both act and compete in the same meristem, it appears that the main shoot meristem is more sensitive to TFL1 rather than floral genes. This spatial analysis therefore reveals how a difference in response helps maintain the ‘veg’ state of the shoot meristem. Oxford University Press 2015-08 2015-05-27 /pmc/articles/PMC4507777/ /pubmed/26019254 http://dx.doi.org/10.1093/jxb/erv247 Text en © The Author 2015. Published by Oxford University Press on behalf of the Society for Experimental Biology. http://creativecommons.org/licenses/by/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Paper
Baumann, Kim
Venail, Julien
Berbel, Ana
Domenech, Maria Jose
Money, Tracy
Conti, Lucio
Hanzawa, Yoshie
Madueno, Francisco
Bradley, Desmond
Changing the spatial pattern of TFL1 expression reveals its key role in the shoot meristem in controlling Arabidopsis flowering architecture
title Changing the spatial pattern of TFL1 expression reveals its key role in the shoot meristem in controlling Arabidopsis flowering architecture
title_full Changing the spatial pattern of TFL1 expression reveals its key role in the shoot meristem in controlling Arabidopsis flowering architecture
title_fullStr Changing the spatial pattern of TFL1 expression reveals its key role in the shoot meristem in controlling Arabidopsis flowering architecture
title_full_unstemmed Changing the spatial pattern of TFL1 expression reveals its key role in the shoot meristem in controlling Arabidopsis flowering architecture
title_short Changing the spatial pattern of TFL1 expression reveals its key role in the shoot meristem in controlling Arabidopsis flowering architecture
title_sort changing the spatial pattern of tfl1 expression reveals its key role in the shoot meristem in controlling arabidopsis flowering architecture
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4507777/
https://www.ncbi.nlm.nih.gov/pubmed/26019254
http://dx.doi.org/10.1093/jxb/erv247
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