Cargando…
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...
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/PMC9070829/ https://www.ncbi.nlm.nih.gov/pubmed/34935983 http://dx.doi.org/10.1093/plphys/kiab589 |
_version_ | 1784700718235516928 |
---|---|
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. |
format | Online Article Text |
id | pubmed-9070829 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT mccreadykirsty targetofrapamycinisessentialforasexualvegetativereproductioninkalanchoe AT spencervictoria targetofrapamycinisessentialforasexualvegetativereproductioninkalanchoe AT jacomeblasquezfrancisco targetofrapamycinisessentialforasexualvegetativereproductioninkalanchoe AT burnettjamie targetofrapamycinisessentialforasexualvegetativereproductioninkalanchoe AT viverossanchezitzelmargarita targetofrapamycinisessentialforasexualvegetativereproductioninkalanchoe AT richeszara targetofrapamycinisessentialforasexualvegetativereproductioninkalanchoe AT kimminsung targetofrapamycinisessentialforasexualvegetativereproductioninkalanchoe |