Skip to main content
European Commission logo print header

Regulatory mechanisms coordinating replication integrity and intra-S repair

Obiettivo

The RecQ family of helicases, including BLM in human and its Saccharomyces cerevisiae homolog Sgs1, have important roles in maintaining genome stability. Sgs1 plays a specific role in response to intra-S DNA damage by resolving the pseudo double HJs resulting from replication-related sister chromatid junctions (SCJs). These catenated DNA structures are thought to represent template switch (TS) intermediates. Although the molecular mechanism is largely unknown, TS is thought to represent a major mechanism to bypass damage during replication. We recently showed that two genetic TS pathways, both of which involve homologous recombination (HR) factors, can lead to bypass of damage by means of SCJs and that their choice is regulated by sumoylation of a key replication factor, PCNA. We also found that the main TS pathway operating in cells involves the coordinated action of HR with the post-replication repair proteins Rad18, Rad5 and Mms2-Ubc13, which exert their role in promoting SCJ formation by means of ubiquitilating PCNA. Previously we showed that the resolution activity of Sgs1 and Top3 is regulated by Ubc9- and Mms21-dependent sumoylation, but the SUMO targets implicated with Sgs1 in this process remained unknown. In this project we plan to characterize the pathways that lead to TS and to understand the factors that promote different steps of this process and their regulation, using in vivo and in vitro approaches. We will attempt to understand how sumoylation is activated by intra-S damage and to address how the formation and subsequent resolution of these X-structures is coordinated with chromatin remodeling functions and topological transitions. We will characterize the X-shaped molecules formed during replication and we will attempt their visualization.

Invito a presentare proposte

ERC-2009-StG
Vedi altri progetti per questo bando

Meccanismo di finanziamento

ERC-SG - ERC Starting Grant

Istituzione ospitante

IFOM-ISTITUTO FONDAZIONE DI ONCOLOGIA MOLECOLARE ETS
Contributo UE
€ 1 841 600,00
Indirizzo
VIA ADAMELLO 16
20139 Milano
Italia

Mostra sulla mappa

Regione
Nord-Ovest Lombardia Milano
Tipo di attività
Research Organisations
Ricercatore principale
Dana Branzei (Dr.)
Contatto amministrativo
Carlo Raimondi Cominesi (Mr.)
Collegamenti
Costo totale
Nessun dato

Beneficiari (1)