Cromie Gareth A, Hyppa Randy W, Taylor Andrew F, Zakharyevich Kseniya, Hunter Neil, Smith Gerald R
Division of Basic Sciences, Fred Hutchinson Cancer Research Center, 1100 Fairview Avenue North, P.O. Box 19024, Seattle, WA 98109, USA.
Cell. 2006 Dec 15;127(6):1167-78. doi: 10.1016/j.cell.2006.09.050.
Crossing-over between homologous chromosomes facilitates their accurate segregation at the first division of meiosis. Current models for crossing-over invoke an intermediate in which homologs are connected by two crossed-strand structures called Holliday junctions. Such double Holliday junctions are a prominent intermediate in Saccharomyces cerevisiae meiosis, where they form preferentially between homologs rather than between sister chromatids. In sharp contrast, we find that single Holliday junctions are the predominant intermediate in Schizosaccharomyces pombe meiosis. Furthermore, these single Holliday junctions arise preferentially between sister chromatids rather than between homologs. We show that Mus81 is required for Holliday junction resolution, providing further in vivo evidence that the structure-specific endonuclease Mus81-Eme1 is a Holliday junction resolvase. To reconcile these observations, we present a unifying recombination model applicable for both meiosis and mitosis in which single Holliday junctions arise from single- or double-strand breaks, lesions postulated by previous models to initiate recombination.
同源染色体之间的交叉互换有助于它们在减数第一次分裂时准确分离。目前关于交叉互换的模型涉及一种中间体,其中同源染色体通过称为霍利迪连接体的两个交叉链结构相连。这种双霍利迪连接体是酿酒酵母减数分裂中的一种突出中间体,它们优先在同源染色体之间而非姐妹染色单体之间形成。与之形成鲜明对比的是,我们发现单霍利迪连接体是粟酒裂殖酵母减数分裂中的主要中间体。此外,这些单霍利迪连接体优先在姐妹染色单体之间而非同源染色体之间出现。我们表明,霍利迪连接体的解离需要Mus81,这进一步提供了体内证据,证明结构特异性核酸内切酶Mus81-Eme1是一种霍利迪连接体解离酶。为了协调这些观察结果,我们提出了一个适用于减数分裂和有丝分裂的统一重组模型,其中单霍利迪连接体源自单链或双链断裂,这些损伤是先前模型假定的启动重组的因素。