PT  - JOURNAL ARTICLE
AU  - Matteo Ferrari
AU  - Chetan C. Rawal
AU  - Samuele Lodovichi
AU  - Achille Pellicioli
TI  - Rad9/53BP1 promotes crossover recombination DNA repair by limiting the Sgs1 and Mph1 helicases
AID  - 10.1101/638791
DP  - 2019 Jan 01
TA  - bioRxiv
PG  - 638791
4099  - http://biorxiv.org/content/early/2019/05/15/638791.short
4100  - http://biorxiv.org/content/early/2019/05/15/638791.full
AB  - A DNA double strand break (DSB) is primed for homologous recombination (HR) repair through the nucleolytic processing (resection) of its ends, leading to the formation of a 3′ single-stranded DNA (ssDNA). Generation of the ssDNA is accompanied by the loading of several repair factors, including the ssDNA binding factor RPA and the recombinase Rad51. Then, depending upon the availability and location of a homologous sequence, different types of HR mechanisms can occur. Inefficient or slow HR repair results in the activation of the DNA damage checkpoint (DDC)1. In budding yeast, the 53BP1 ortholog Rad9 acts as a scaffold, mediating signal from upstream kinases Mec1 and Tel1 (ATR and ATM in human) to downstream effectors kinases Rad53 and Chk1 (CHK2 and CHK1 in human). In addition to its role in DDC, Rad9 limits DSB resection 2. Remarkably, this function is conserved in 53BP1, also being implicated in cancer biology in human cells 3,4.Here we show that Rad9 limits the recruitment of the helicases Sgs1 and Mph1 on to a DSB, promoting Rad51-dependent recombination with long track DNA conversions, crossovers and break-induced replication (BIR). This regulation couples the DDC with the choice and effectiveness of HR sub-pathways, and might be critical to limit genome instability with implication for cancer research.