Skip to main content
Go to the home page of the European Commission (opens in new window)
English en
CORDIS - EU research results
CORDIS

TOR-mediated translational control of cytokinin homeostasis in shoot apical meriSTEM

Project description

How TOR controls plant growth

Growth and organ formation in plants depend on signals that link metabolism to development. The shoot apical meristem (SAM) is the plant’s growth engine – a tissue responsible for producing new cells and initiating organs. The TOR kinase is a key metabolic regulator activated by light and sugar, which is central to SAM function. TOR promotes the expression of a critical stem cell regulator called WUSCHEL and maintains cytokinin levels by inhibiting the production of cytokinin-degrading enzymes. Supported by the Marie Skłodowska-Curie Actions programme, the TORcySTEM project will investigate the molecular mechanisms underlying this regulation, identify TOR-sensitive elements in cytokinin-related genes, and uncover proteins that mediate TOR effects.

Objective

Plant growth and organogenesis depend on the ability of meristems to integrate metabolic signals with developmental pathways. The shoot apical meristem (SAM) is a key developmental hub where nutrient availability and hormonal cues, particularly cytokinin, coordinate cell proliferation and organ initiation. The conserved kinase Target of Rapamycin (TOR) acts as a central regulator of these inputs, and its activity is essential for meristem activation and stem cell maintenance. Work from the host lab has shown that light and sugar activate TOR, which in turn promotes expression of the stem cell regulator WUSCHEL (WUS) and enables proper SAM function. Recent findings further reveal that TOR sustains shoot growth by repressing the translation of CKX transcripts, which encode cytokinin-degrading enzymes, thereby preserving cytokinin levels required for WUS expression and meristem activity. However, the mechanism behind this selective translational control remains unknown.

TORcySTEM (TOR–cytokinin–merisSTEM axis) will dissect this regulatory pathway through three objectives:

1) Identify TOR-sensitive cis-regulatory elements within CKX transcripts;
2) Discover TOR-regulated trans-acting effector proteins;
3) Establish how this control shapes cytokinin signaling and SAM function.

Together, these aims will uncover how TOR-dependent translational control fine-tunes cytokinin homeostasis and stem cell activity, providing a mechanistic link between metabolism and shoot development.

Fields of science (EuroSciVoc)

This project has not yet been classified with EuroSciVoc.
Be the first one to suggest relevant scientific fields and help us improve our classification service

Keywords

Programme(s)

Topic(s)

Funding Scheme

HORIZON-TMA-MSCA-PF-EF - HORIZON TMA MSCA Postdoctoral Fellowships - European Fellowships

See all projects funded under this funding scheme

Call for proposal

(opens in new window) HORIZON-MSCA-2025-PF

See all projects funded under this call

Coordinator

RUPRECHT-KARLS-UNIVERSITAET HEIDELBERG
Net EU contribution
€ 217 965,12
Address
SEMINARSTRASSE 2
69117 Heidelberg
Germany
Region
Baden-Württemberg Karlsruhe Heidelberg, Stadtkreis
Activity type
Higher or Secondary Education Establishments
Links
Total cost
No data