NHEJ regulation by mating type is exercised through a novel protein, Lif2p, essential to the Ligase IV pathway

Abstract

In the yeast Saccharomyces cerevisiae, DNA double strand break (DSB) repair by nonhomologous end-joining (NHEJ) requires the DNA end-binding heterodimer Yku70p–Yku80p and the ligase Dnl4p associated with its cofactor Lif1p. NHEJ efficiency is down-regulated inMATa/MATα cells relative to MATa or MATαcells, but the mechanism of this mating type regulation is unknown. Here we report the identification of Lif2p, a S. cerevisiaeprotein that interacts with Lif1p in a two-hybrid system. Disruption ofLIF2 abolishes the capacity of cells to repair DSBs by end-joining to the same extent than lif1 and dnl4mutants. In MATa/MATα cells, Lif2p steady-state level is strongly repressed when other factors involved in NHEJ are unaffected. Increasing the dosage of the Lif2p protein can suppress the NHEJ defect in a/α cells. Together, these results indicate that NHEJ regulation by mating type is achieved, at least in part, by a regulation of Lif2p activity.

Keywords

• DNA repair
• end-joining
• HO
• I-SceI
• a/α repression