Deciphering the Regulatory Logic of Cortical Development
EpiCortex aims to map the regulatory landscape of mouse cortical development across timepoints to understand neuronal lineage specification and improve therapeutic strategies for neuropsychiatric diseases.
Projectdetails
Introduction
The mammalian cortex is the most complex region of the brain responsible for higher cognitive functions. Abnormal cortical development often translates into prominent neuropsychiatric diseases, which affect different neuronal subtypes with unique molecular and morphological features. Increasing evidence suggests that epigenetic regulation is essential for cortical development, but how multiple regulatory layers are coordinated to specify distinct neuronal lineages in vivo remains unclear.
Research Approach
My team and I recently applied single-cell RNA-seq, single-cell ATAC-seq together with cell-type-specific DNA methylation and 3D genome measurements to map the regulatory landscape of neural differentiation at a single embryonic stage in vivo. However, the process of neuronal subtype specification involves multiple distinct waves of differentiation over several consecutive days.
Objectives
To decode the molecular logic of temporal cellular identity in the cortex, I will comprehensively dissect the interplay between gene expression, chromatin topology, and epigenetics in specifying cell fate. In order to accomplish this, I will build upon my extensive experimental and computational expertise to:
- Map the regulatory landscape of the developing mouse cortex across multiple regulatory layers and timepoints in single cells.
- Identify and validate cis-regulatory elements via a novel massive parallel cell-type specific reporter assay in vivo.
- Determine the functional consequences of perturbing enhancers and silencers using a highly multiplexed single-cell approach.
Expected Outcomes
Collectively, EpiCortex will provide unprecedented insights and establish new paradigms into the interplay between transcription factors, epigenome dynamics, and gene expression in development. It will allow us to better understand the molecular logic of lineage specification in the mammalian cortex and more precisely define, compare, and ultimately engineer cellular identities for therapeutic and regenerative purposes.
Financiële details & Tijdlijn
Financiële details
Subsidiebedrag | € 1.999.643 |
Totale projectbegroting | € 1.999.643 |
Tijdlijn
Startdatum | 1-1-2023 |
Einddatum | 31-12-2027 |
Subsidiejaar | 2023 |
Partners & Locaties
Projectpartners
- HELMHOLTZ ZENTRUM MUENCHEN DEUTSCHES FORSCHUNGSZENTRUM FUER GESUNDHEIT UND UMWELT GMBHpenvoerder
Land(en)
Vergelijkbare projecten binnen European Research Council
Project | Regeling | Bedrag | Jaar | Actie |
---|---|---|---|---|
Translational Control of Neuronal Fate and IdentityThis project aims to investigate how translational control via mature tRNA availability regulates gene expression and neuronal diversity during cortical development in mice. | ERC Consolid... | € 2.000.000 | 2023 | Details |
Revealing the wiring rules of neural circuit assembly with spatiotemporally resolved molecular connectomicsThis project aims to develop a novel method for large-scale neural circuit tracing and RNA sequencing to understand genomic influences on brain connectivity and its implications for autism. | ERC Starting... | € 1.500.000 | 2024 | Details |
Systematically Dissecting the Regulatory Logic of Chromatin ModificationsThis project aims to systematically investigate the functional impact of chromatin modifications on gene expression using a novel editing platform to enhance precision medicine and understand epigenomic profiles. | ERC Consolid... | € 1.999.565 | 2023 | Details |
Uncovering the role and regulation of 3D DNA-RNA nuclear dynamics in controlling cell fate decisionsThis project aims to elucidate the interplay between 3D genome organization and transcriptome dynamics in early mouse embryos to identify factors influencing cell fate decisions. | ERC Starting... | € 1.500.000 | 2023 | Details |
Development of novel single cell multi-omics methods to uncover regulators of cell type specific epigenetic states.scEpiTarget aims to develop novel single-cell methods to identify factors regulating cell-type specific histone modifications, enhancing understanding of epigenetic control in cell differentiation and potential therapies. | ERC Starting... | € 1.810.745 | 2025 | Details |
Translational Control of Neuronal Fate and Identity
This project aims to investigate how translational control via mature tRNA availability regulates gene expression and neuronal diversity during cortical development in mice.
Revealing the wiring rules of neural circuit assembly with spatiotemporally resolved molecular connectomics
This project aims to develop a novel method for large-scale neural circuit tracing and RNA sequencing to understand genomic influences on brain connectivity and its implications for autism.
Systematically Dissecting the Regulatory Logic of Chromatin Modifications
This project aims to systematically investigate the functional impact of chromatin modifications on gene expression using a novel editing platform to enhance precision medicine and understand epigenomic profiles.
Uncovering the role and regulation of 3D DNA-RNA nuclear dynamics in controlling cell fate decisions
This project aims to elucidate the interplay between 3D genome organization and transcriptome dynamics in early mouse embryos to identify factors influencing cell fate decisions.
Development of novel single cell multi-omics methods to uncover regulators of cell type specific epigenetic states.
scEpiTarget aims to develop novel single-cell methods to identify factors regulating cell-type specific histone modifications, enhancing understanding of epigenetic control in cell differentiation and potential therapies.