Revealing novel molecular mechanisms linking DNA replication and cell fate decisions

Informations projet

RepDiff

N° de convention de subvention: 846375

DOI

10.3030/846375

Projet clôturé

Date de signature de la CE 10 Avril 2019

Date de début 1 Janvier 2020

Date de fin 31 Decembre 2021

Financé au titre de

• EXCELLENT SCIENCE - Marie Skłodowska-Curie Actions

Coût total

€ 219 312,00

Contribution de l’UE

€ 219 312,00

Coordonné par

KOBENHAVNS UNIVERSITET
Denmark

Periodic Reporting for period 1 - RepDiff (Revealing novel molecular mechanisms linking DNA replication and cell fate decisions)

Période du rapport: 2020-01-01 au 2021-12-31

Résumé du contexte et des objectifs généraux du projet

During normal development our cells go through programmed changes in cell identity that alter their properties. In diseases like cancer, our cells undergo unscheduled changes in cell identity. Cell division play a major role in both processes. To divide, the genetic code must be copied to be transferred to both daughter cells, and this entails a transient disruption of the chromatin landscape that organises and regulates the genome. The window of chromatin replication may represent an important opportunity to facilitate chromatin reorganisation for cell reprogramming towards a different identity. In this project I sought to explore this hypothesis by identifying chromatin replication and restoration proteins which have a role in maintaining the pluripotent state and the engagement of mouse embryonic stem cells into differentiation. This insight will advance our understanding of mechanisms which take action in normal and abnormal cell fate transitions. This work, although not yet finalized, revealed novel link between chromatin replication and stem cell potency.

Travail effectué depuis le début du projet jusqu’à la fin de la période considérée dans le rapport et principaux résultats atteints jusqu’à présent

I characterised chromatin replication proteins which play a role in stem cell plasticity. This work links chromatin replication and restoration, epigenetic inheritance and developmental competence of mouse stem cells. Publication of this work will provide a new understanding of cellular plasticity and open new research avenues in epigenetics and stem cell biology.

Progrès au-delà de l’état des connaissances et impact potentiel prévu (y compris l’impact socio-économique et les conséquences sociétales plus larges du projet jusqu’à présent)

This work provided new link between chromatin replication and restoration, epigenetic inheritance and mouse embryonic cellular plasticity. This work results could create new working model to delineate mechanisms which underpin abnormal cell fate transitions, as in cancer.

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