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Temporal reconstruction of tRNA abundance during cortical development in progenitor cells

Project description

Regulatory insight into cortical development

The cerebral cortex is the neuronal outer layer of our brain and is responsible for cognitive functions including memory, thinking and learning. Cortical neurons are diverse and arise from multipotent progenitors. Single-cell transcriptomics studies have shown that transcriptional programmes are responsible for this neuronal diversity, but discrepancies between abundance of mRNAs and proteins suggest additional regulatory mechanisms. Funded by the Marie Skłodowska-Curie Actions programme, the TRANSITION project focuses on the role of transfer RNA (tRNA) in refining gene expression during neurodevelopment and cortical patterning. By examining tRNA abundance and translation efficiency during development, the study aims to identify new genes crucial for cortical development, offering a new model for neuronal diversity regulation.

Objective

The cerebral cortex with its range of specialized excitatory projection neurons is essential to the high-order cognitive functions of the brain. These hundreds of subtypes of projection neurons arise from a uniform pool of multipotent apical progenitors (APs) which sequentially generate neuronal progeny with distinct fates over time.
Recent technological advances in single cell transcriptomics revealed the existence transcriptional programs that seed neuronal diversity. While this working model provides a good explanation for the developmental origin of the distinct neuronal subtypes, it is flawed by the existence of some non-correlating mRNAs and proteins. Indeed, a significant fraction of mRNA that characterizes mature neurons can already be found untranslated in progenitors. The additional mechanisms that coordinate the protein synthesis and ensure correct protein expression in progenitors and daughter neurons have not been identified yet. This project focuses on solving the timely question of which mechanisms, synergically with transcription, are required to refine gene expression during neurodevelopment and cortical patterning.
To do so, we explore the role of translation and its critical adaptor molecule, the transfer RNA (tRNA), in regulating the competency of APs to generate distinct neuronal fate during mouse embryonic cortices development. We will generate a comprehensive view of tRNAs abundance and translation efficiency in APs at ages E12 to E17. This will uncover a novel regulatory role for tRNAs, updating the conventional view of them as housekeeping genes, and find new candidate genes for cortical development in both health and disease. All in all, we will provide a new working model for how neuronal fate and diversity are regulated and opens avenues for future research in other developmental fields where translation has been previously overlooked.

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

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Call for proposal

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(opens in new window) HORIZON-MSCA-2023-PF-01

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Coordinator

CENTRE EUROPEEN DE RECHERCHE EN BIOLOGIE ET MEDECINE
Net EU contribution

Net EU financial contribution. The sum of money that the participant receives, deducted by the EU contribution to its linked third party. It considers the distribution of the EU financial contribution between direct beneficiaries of the project and other types of participants, like third-party participants.

€ 195 914,88
Address
Rue Laurent Fries 1
67404 Illkirch Graffenstaden
France

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Region
Grand Est Alsace Bas-Rhin
Activity type
Research Organisations
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