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TARGET OF RAPAMYCIN is essential for asexual vegetative reproduction in Kalanchoë

The unique mechanism by which leaf margin cells regain potency and then form a plantlet in Kalanchoë spp. remains elusive but involves organogenesis and embryogenesis in response to age, day length, nutrient availability, and drought stress. In light of this, we investigated whether TARGET OF RAPAMY...

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Autores principales: McCready, Kirsty, Spencer, Victoria, Jácome-Blásquez, Francisco, Burnett, Jamie, Viveros Sánchez, Itzel Margarita, Riches, Zara, Kim, Minsung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9070829/
https://www.ncbi.nlm.nih.gov/pubmed/34935983
http://dx.doi.org/10.1093/plphys/kiab589
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author McCready, Kirsty
Spencer, Victoria
Jácome-Blásquez, Francisco
Burnett, Jamie
Viveros Sánchez, Itzel Margarita
Riches, Zara
Kim, Minsung
author_facet McCready, Kirsty
Spencer, Victoria
Jácome-Blásquez, Francisco
Burnett, Jamie
Viveros Sánchez, Itzel Margarita
Riches, Zara
Kim, Minsung
author_sort McCready, Kirsty
collection PubMed
description The unique mechanism by which leaf margin cells regain potency and then form a plantlet in Kalanchoë spp. remains elusive but involves organogenesis and embryogenesis in response to age, day length, nutrient availability, and drought stress. In light of this, we investigated whether TARGET OF RAPAMYCIN (TOR), a conserved protein kinase in eukaryotes that controls cell growth and metabolism in response to nutrient and energy availability, may regulate plantlet formation. Kalanchoë daigremontiana TOR (KdTOR) was expressed in the leaf margin at the site of plantlet initiation, in the early plantlet cotyledons, and in the root tip of the developed plantlet. Both chemical and genetic inhibition of TOR Kinase activity in Kalanchoë daigremontiana leaves disrupted plantlet formation. Furthermore, downregulation of KdTOR in transgenic plants led to wide-ranging transcriptional changes, including decreased K. daigremontiana SHOOTMERISTEMLESS and K. daigremontiana LEAFYCOTYLEDON1 expression, whereas auxin treatments induced KdTOR expression in the plantlet roots. These results suggest that the KdTOR pathway controls plantlet development in cooperation with auxin, organogenesis, and embryogenesis pathways. The ancient and highly conserved TOR Kinase therefore controls diverse and unique developmental pathways, such as asexual reproduction within the land plant lineage.
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spelling pubmed-90708292022-05-06 TARGET OF RAPAMYCIN is essential for asexual vegetative reproduction in Kalanchoë McCready, Kirsty Spencer, Victoria Jácome-Blásquez, Francisco Burnett, Jamie Viveros Sánchez, Itzel Margarita Riches, Zara Kim, Minsung Plant Physiol Research Articles The unique mechanism by which leaf margin cells regain potency and then form a plantlet in Kalanchoë spp. remains elusive but involves organogenesis and embryogenesis in response to age, day length, nutrient availability, and drought stress. In light of this, we investigated whether TARGET OF RAPAMYCIN (TOR), a conserved protein kinase in eukaryotes that controls cell growth and metabolism in response to nutrient and energy availability, may regulate plantlet formation. Kalanchoë daigremontiana TOR (KdTOR) was expressed in the leaf margin at the site of plantlet initiation, in the early plantlet cotyledons, and in the root tip of the developed plantlet. Both chemical and genetic inhibition of TOR Kinase activity in Kalanchoë daigremontiana leaves disrupted plantlet formation. Furthermore, downregulation of KdTOR in transgenic plants led to wide-ranging transcriptional changes, including decreased K. daigremontiana SHOOTMERISTEMLESS and K. daigremontiana LEAFYCOTYLEDON1 expression, whereas auxin treatments induced KdTOR expression in the plantlet roots. These results suggest that the KdTOR pathway controls plantlet development in cooperation with auxin, organogenesis, and embryogenesis pathways. The ancient and highly conserved TOR Kinase therefore controls diverse and unique developmental pathways, such as asexual reproduction within the land plant lineage. Oxford University Press 2021-12-22 /pmc/articles/PMC9070829/ /pubmed/34935983 http://dx.doi.org/10.1093/plphys/kiab589 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
McCready, Kirsty
Spencer, Victoria
Jácome-Blásquez, Francisco
Burnett, Jamie
Viveros Sánchez, Itzel Margarita
Riches, Zara
Kim, Minsung
TARGET OF RAPAMYCIN is essential for asexual vegetative reproduction in Kalanchoë
title TARGET OF RAPAMYCIN is essential for asexual vegetative reproduction in Kalanchoë
title_full TARGET OF RAPAMYCIN is essential for asexual vegetative reproduction in Kalanchoë
title_fullStr TARGET OF RAPAMYCIN is essential for asexual vegetative reproduction in Kalanchoë
title_full_unstemmed TARGET OF RAPAMYCIN is essential for asexual vegetative reproduction in Kalanchoë
title_short TARGET OF RAPAMYCIN is essential for asexual vegetative reproduction in Kalanchoë
title_sort target of rapamycin is essential for asexual vegetative reproduction in kalanchoë
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9070829/
https://www.ncbi.nlm.nih.gov/pubmed/34935983
http://dx.doi.org/10.1093/plphys/kiab589
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