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Deciphering the evolution and roles of cytosine DNA methylation across eukaryotes

Project description

The evolution of the epigenetic mechanism of DNA methylation

Cytosine DNA methylation is a major form of DNA modification in the genome that plays a critical role in chromatin structure and gene expression. The methylation of silent transposable elements and constitutively transcribed genes is the best-studied DNA methylation process in vertebrates, plants and fungi. The methylation genes are not always orthologous across divergent lineages and could be the products of convergent evolution. The EU-funded METHYLEVOL project will study the evolution of DNA methylation, determining its role across eukaryotic diversity. Using state-of-the-art genomic techniques, experimental manipulations and computational analyses, the research will link experimental epigenomics to macro-evolutionary comparative genomics, revealing functions of DNA methylation assembled throughout evolution.

Objective

Cytosine DNA methylation is a major component of eukaryotic chromatin, yet extensive variation of methylation patterns occurs throughout eukaryotes. So far, the roles of DNA methylation have been mostly characterized in vertebrates, plants and fungi, where two common patterns have emerged as potentially ancestral within eukaryotes: methylation of silent transposable elements and methylation of constitutively transcribed genes (gene body methylation). However, the genes responsible for depositing methylation are not always orthologous across divergent lineages, so these common patterns could instead be the product of convergent evolution. To discern between these alternatives, we first need to correct the taxon sampling bias that hampers our understanding about the evolution of DNA methylation.
In this project we will determine the roles of DNA methylation across vastly underexplored eukaryotic diversity. We will use state-of-the-art genomic techniques, experimental manipulations and computational analyses to trace the evolutionary conservation of methylation-dependent transposable element silencing across a wide range of unicellular eukaryotes, using methylation-depleting drugs and bisulfite sequencing. We will then assess the roles of gene body methylation in an invertebrate to unveil similarities with plants and shed light on why vertebrates transitioned to hypermethylated genomes. Finally, we will study the evolution of proteins able to bind and interpret DNA methylation across disparate eukaryotes, since ultimately these proteins link DNA methylation and its regulatory functions.
Through linking experimental epigenomics to macro-evolutionary comparative genomics this project will reveal how different functions of DNA methylation assembled throughout evolution. In turn, this evolutionary perspective will allow a better understanding of the genome regulatory roles of this base modification and its impact on genome composition in plants and animals.

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ERC-STG - Starting Grant

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Call for proposal

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(opens in new window) ERC-2020-STG

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Host institution

QUEEN MARY UNIVERSITY OF LONDON
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.

€ 1 499 965,00
Address
327 MILE END ROAD
E1 4NS LONDON
United Kingdom

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Activity type
Higher or Secondary Education Establishments
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Total cost

The total costs incurred by this organisation to participate in the project, including direct and indirect costs. This amount is a subset of the overall project budget.

€ 1 499 965,00

Beneficiaries (1)

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