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MetabolACE

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Histone modifying enzymes as direct regulators of metabolic reprogramming Towar...

Histone modifying enzymes as direct regulators of metabolic reprogramming Towards a New Paradigm Accumulating evidence in recent years has highlighted strong regulatory interactions between epigenetic mechanisms and metabolic transformations, mainly through transcriptional control of key metabolic genes. However, what has bee... ver más

31/12/2022

UCY

146K€

Presupuesto del proyecto: 146K€

Líder del proyecto

UNIVERSITY OF CYPRUS No se ha especificado una descripción o un objeto social para esta compañía.

TRL 4-5

Fecha límite participación Sin fecha límite de participación.

Financiación concedida El organismo H2020 notifico la concesión del proyecto el día 2022-12-31

MSCA-IF-2019: Individual Fellowships

I+D

Cerrada hace 5 años

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Información adicional privada

No hay información privada compartida para este proyecto. Habla con el coordinador.

1 Participantes

UCY

145.94K€ | Lider

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Duración del proyecto: 32 meses Fecha Inicio: 2020-04-07
Fecha Fin: 2022-12-31

Líder del proyecto

UNIVERSITY OF CYPRUS No se ha especificado una descripción o un objeto social para esta compañía.

TRL 4-5

Presupuesto del proyecto 146K€

Fecha límite de participación Sin fecha límite de participación.

Descripción del proyecto Accumulating evidence in recent years has highlighted strong regulatory interactions between epigenetic mechanisms and metabolic transformations, mainly through transcriptional control of key metabolic genes. However, what has been overlooked is the direct effect of histone modifying enzymes on cellular metabolism as they are large consumers of sentinel metabolites. Therefore, I hypothesize that histone modifying enzymes and their mediated post-translation modifications (PTMs) on histones directly drive metabolic rewiring which subsequently impacts various cellular processes including gene expression. Specifically, this fellowship will focus on histone acetyltransferases (HATs) that use acetyl coenzyme A (Acetyl-CoA) as their sole substrate. Using interdisciplinary, state-of-the-art approaches that integrate subcellular metabolomics and high-throughput epigenomic techniques I will interrogate how the activity of HATs controls the abundance of acetyl-CoA and, in turn, defines the metabolic status of a cell leading to a subsequent reciprocal effect on the epigenetic landscape and genome regulation. Firm preliminary data, that I have recently generated, support the proposed project hypothesis and demonstrate that the experimental design is credible. During this project, my in-depth knowledge of metabolism and mass spectrometry skills will be combined with the expertise of epigenetics and histone biology that I will acquire at the host lab to reveal a new pathway through which histone PTMs function. This work will unveil a new fundamental link between epigenetics and metabolism and will be the commencing point for important future work in health and disease. Importantly, this fellowship will propel my academic career and help me become a scientific leader at the interface of epigenetics and metabolism since it will act as a stepping stone towards securing new research funding and acquiring a tenure track position.

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