📋 Tender Overview
Systematically Dissecting The Regulatory Logic Of Chromatin Modifications
Insight Into The Functional Significance Of Chromatin Modificationschromatin Modifications Are Dynamic Chemical Alterations In Histones And Dna Affecting Access Of Transcription Proteins To Genomic Dna, Thereby Controlling Gene Expression. However, Understanding The Exact Functions Of These Modifications Has Been Challenging Due To Limited Tools. Funded By The European Research Council, The Modlogic Project Proposes To Develop An Epigenome Editing Platform For Investigating Chromatin Modifications In Various Cellular Contexts. The Rationale Is To Study The Functional Outcome Of Individual Modifications At Single-Cell Resolution Across Different Developmental Stages. This Comprehensive Research Will Uncover How Chromatin States Interact With Genomic Elements And Cell Identity To Influence Gene Expression In Health And Disease.
Funded Under
European Research Council (Erc)
Total Cost
€ 1 999 565,00
Eu Contribution
€ 1 999 565,00
Coordinated By
European Molecular Biology Laboratory
Germany
Objective
Chromatin modifications are a key mechanism for regulating gene expression patterns in normal and disease settings. Nonetheless, despite the ubiquity of epigenomics data, the causal functions of specific chromatin modifications have proved challenging to unravel. This knowledge gap reflects limited approaches to dissect how chromatin modifications influence transcription quantitatively and context-dependently, across diverse genomic features or variants in any given cell-type. Here, we propose to systematically interrogate the functional impact of specific- and combinatorial- chromatin modifications within tens-of-thousands of contexts in living cells, using a novel modular epigenome editing platform. We will produce the largest precision chromatin-perturbation dataset to date, and exploit it to capture multi-modal functional responses at allelically-resolved single-cell resolution, across developmental lineages. The unprecedented scale of the work will uncover the regulatory logic by which distinct chromatin states interact with genomic motifs, sequence variants, and cellular identity, to shape quantitative gene expression patterns. By integrating data and deploying genetic screens, we will further identify the trans-acting and cis-structural mechanisms that underpin complex relationships. Our technology will circumvent the key limitations of existing approaches, by excluding pleiotropy and redundancy, whilst systematically isolating functional genome x epigenome interactions. The cumulative insights will be used to build a predictive model based on rational rules for how specific changes in chromatin marks instruct - or reflect - gene expression states within specific contexts. This will aid design strategies for precision medicine, and create guiding principles to attribute functional significance to epigenome profiles in health and disease
