Departamento de Bioquímica e Bioloxía Molecular, CIMUS, Universidade de Santiago de Compostela-Instituto de Investigación Sanitaria (IDIS), Santiago de Compostela, Spain.
Methods Mol Biol. 2021;2153:169-185. doi: 10.1007/978-1-0716-0644-5_12.
Holliday junctions are four-way DNA structures that may arise during meiotic recombination, double-strand break repair, or postreplicative repair by the reciprocal exchange of single strands between two DNA molecules. Given their ability to effectively bridge two sister chromatids or homologous chromosomes, cells have implemented various pathways to ensure their timely removal. One of them is the nucleolytic processing of the Holliday junctions by specialized structure-selective endonucleases termed resolvases, which sever the connection between the linked molecules. These Holliday junction resolvases are essential tools of the DNA damage repair machinery to ensure accurate chromosomal segregation, whose activities can be modulated by posttranslational modifications like phosphorylation. Here, we describe a protocol to purify S. cerevisiae Yen1 resolvase in two different phosphorylation states (high and low) and to set up a biochemical assay to compare their ability to process a synthetic, oligonucleotide-based Holliday junction structures.
Holliday 连接点是一种四链 DNA 结构,可能在减数分裂重组、双链断裂修复或复制后通过两个 DNA 分子之间单链的相互交换而产生。鉴于其有效桥接两个姐妹染色单体或同源染色体的能力,细胞已经实施了各种途径来确保其及时去除。其中之一是通过称为核酸酶的专门结构选择性内切核酸酶对 Holliday 连接点进行核酶处理,从而切断连接分子之间的连接。这些 Holliday 连接点核酸酶是 DNA 损伤修复机制的重要工具,可确保染色体正确分离,其活性可通过磷酸化等翻译后修饰来调节。在这里,我们描述了一种在两种不同磷酸化状态(高和低)下纯化 S. cerevisiae Yen1 核酸酶的方案,并建立了一种生化测定法来比较它们处理合成的基于寡核苷酸的 Holliday 连接点结构的能力。