Department of Microbiology and Immunology, Columbia University Medical Center, New York, New York, USA.
Nat Struct Mol Biol. 2012 Sep;19(9):964-71. doi: 10.1038/nsmb.2359. Epub 2012 Aug 12.
Holliday junctions can be formed during homology-dependent repair of DNA double-strand breaks, and their resolution is essential for chromosome segregation and generation of crossover products. The Mus81-Mms4 and Yen1 nucleases are required for mitotic crossovers between chromosome homologs in Saccharomyces cerevisiae; however, crossovers between dispersed repeats are still detected in their absence. Here we show that the Rad1-Rad10 nuclease promotes formation of crossover and noncrossover recombinants between ectopic sequences. Crossover products were not recovered from the mus81Δ rad1Δ yen1Δ triple mutant, indicating that all three nucleases participate in processing recombination intermediates that form between dispersed repeats. We suggest a new mechanism for crossovers that involves Rad1-Rad10 clipping and resolution of a single Holliday junction-containing intermediate by Mus81-Mms4 or Yen1 cleavage or by replication. Consistent with the model, we show accumulation of Rad1-dependent joint molecules in the mus81Δ yen1Δ mutant.
Holliday 连接点可在 DNA 双链断裂的同源依赖性修复过程中形成,其解决对于染色体分离和交叉产物的产生至关重要。在酿酒酵母中,Mus81-Mms4 和 Yen1 核酸酶对于染色体同源物之间的有丝分裂交叉是必需的;然而,在它们缺失的情况下,仍能检测到分散重复序列之间的交叉。在这里,我们表明 Rad1-Rad10 核酸酶促进异位序列之间交叉和非交叉重组体的形成。在 mus81Δ rad1Δ yen1Δ 三重突变体中未回收交叉产物,表明这三种核酸酶都参与了在分散重复序列之间形成的重组中间体的加工。我们提出了一个新的交叉机制,该机制涉及 Rad1-Rad10 的剪接,以及 Mus81-Mms4 或 Yen1 切割或复制来解决单个含有 Holliday 连接点的中间产物。与该模型一致,我们表明在 mus81Δ yen1Δ 突变体中积累了依赖 Rad1 的联合分子。