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Glc-TOR signalling leads transcriptome reprogramming and meristem activation

Meristems encompass stem/progenitor cells that sustain postembryonic growth of all plant organs. How meristems are activated and sustained by nutrient signalling remains enigmatic in photosynthetic plants. Combining chemical manipulations and chemical genetics at the photoautotrophic transition chec...

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Autores principales: Xiong, Yan, McCormack, Matthew, Li, Lei, Hall, Qi, Xiang, Chengbin, Sheen, Jen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4140196/
https://www.ncbi.nlm.nih.gov/pubmed/23542588
http://dx.doi.org/10.1038/nature12030
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author Xiong, Yan
McCormack, Matthew
Li, Lei
Hall, Qi
Xiang, Chengbin
Sheen, Jen
author_facet Xiong, Yan
McCormack, Matthew
Li, Lei
Hall, Qi
Xiang, Chengbin
Sheen, Jen
author_sort Xiong, Yan
collection PubMed
description Meristems encompass stem/progenitor cells that sustain postembryonic growth of all plant organs. How meristems are activated and sustained by nutrient signalling remains enigmatic in photosynthetic plants. Combining chemical manipulations and chemical genetics at the photoautotrophic transition checkpoint, we reveal that shoot photosynthesis-derived glucose drives target-of-rapamycin (TOR) signalling relays through glycolysis and mitochondrial bioenergetics to control root meristem activation, which is decoupled from direct glucose sensing, growth-hormone signalling, and stem-cell maintenance. Surprisingly, glucose-TOR signalling dictates transcriptional reprogramming of remarkable gene sets involved in central and secondary metabolism, cell cycle, transcription, signalling, transport and folding. Systems, cellular and genetic analyses uncover TOR phosphorylation of E2Fa transcription factor for an unconventional activation of S-phase genes, and glucose-signalling defects in e2fa root meristems. Our findings establish pivotal roles of glucose-TOR signalling in unprecedented transcriptional networks wiring central metabolism and biosynthesis for energy and biomass production, and integrating localized stem/progenitor-cell proliferation through inter-organ nutrient coordination to control developmental transition and growth.
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spelling pubmed-41401962014-08-21 Glc-TOR signalling leads transcriptome reprogramming and meristem activation Xiong, Yan McCormack, Matthew Li, Lei Hall, Qi Xiang, Chengbin Sheen, Jen Nature Article Meristems encompass stem/progenitor cells that sustain postembryonic growth of all plant organs. How meristems are activated and sustained by nutrient signalling remains enigmatic in photosynthetic plants. Combining chemical manipulations and chemical genetics at the photoautotrophic transition checkpoint, we reveal that shoot photosynthesis-derived glucose drives target-of-rapamycin (TOR) signalling relays through glycolysis and mitochondrial bioenergetics to control root meristem activation, which is decoupled from direct glucose sensing, growth-hormone signalling, and stem-cell maintenance. Surprisingly, glucose-TOR signalling dictates transcriptional reprogramming of remarkable gene sets involved in central and secondary metabolism, cell cycle, transcription, signalling, transport and folding. Systems, cellular and genetic analyses uncover TOR phosphorylation of E2Fa transcription factor for an unconventional activation of S-phase genes, and glucose-signalling defects in e2fa root meristems. Our findings establish pivotal roles of glucose-TOR signalling in unprecedented transcriptional networks wiring central metabolism and biosynthesis for energy and biomass production, and integrating localized stem/progenitor-cell proliferation through inter-organ nutrient coordination to control developmental transition and growth. 2013-03-31 2013-04-11 /pmc/articles/PMC4140196/ /pubmed/23542588 http://dx.doi.org/10.1038/nature12030 Text en Users may view, print, copy, download and text and data- mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Xiong, Yan
McCormack, Matthew
Li, Lei
Hall, Qi
Xiang, Chengbin
Sheen, Jen
Glc-TOR signalling leads transcriptome reprogramming and meristem activation
title Glc-TOR signalling leads transcriptome reprogramming and meristem activation
title_full Glc-TOR signalling leads transcriptome reprogramming and meristem activation
title_fullStr Glc-TOR signalling leads transcriptome reprogramming and meristem activation
title_full_unstemmed Glc-TOR signalling leads transcriptome reprogramming and meristem activation
title_short Glc-TOR signalling leads transcriptome reprogramming and meristem activation
title_sort glc-tor signalling leads transcriptome reprogramming and meristem activation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4140196/
https://www.ncbi.nlm.nih.gov/pubmed/23542588
http://dx.doi.org/10.1038/nature12030
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