Rtt107 Phosphorylation Promotes Localisation to DNA Double-Stranded Breaks DSBs and Recombinational Repair between Sister ChromatidsReportar como inadecuado




Rtt107 Phosphorylation Promotes Localisation to DNA Double-Stranded Breaks DSBs and Recombinational Repair between Sister Chromatids - Descarga este documento en PDF. Documentación en PDF para descargar gratis. Disponible también para leer online.

Efficient repair of DNA double-stranded breaks DSB requires a coordinated response at the site of lesion. Nucleolytic resection commits repair towards homologous recombination, which preferentially occurs between sister chromatids. DSB resection promotes recruitment of the Mec1 checkpoint kinase to the break. Rtt107 is a target of Mec1 and serves as a scaffold during repair. Rtt107 plays an important role during rescue of damaged replication forks, however whether Rtt107 contributes to the repair of DSBs is unknown. Here we show that Rtt107 is recruited to DSBs induced by the HO endonuclease. Rtt107 phosphorylation by Mec1 and its interaction with the Smc5–Smc6 complex are both required for Rtt107 loading to breaks, while Rtt107 regulators Slx4 and Rtt101 are not. We demonstrate that Rtt107 has an effect on the efficiency of sister chromatid recombination SCR and propose that its recruitment to DSBs, together with the Smc5–Smc6 complex is important for repair through the SCR pathway.



Autor: Pranav Ullal, Felipe Vilella-Mitjana, Adam Jarmuz, Luis Aragón

Fuente: http://plos.srce.hr/



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