Structural Biology Program, Sloan Kettering Institute, New York, NY, USA.
Department of Chemistry, Université du Québec à Montréal, Montréal, QC, Canada.
EMBO J. 2021 Nov 15;40(22):e103787. doi: 10.15252/embj.2019103787. Epub 2021 Sep 29.
Repair of DNA double-stranded breaks by homologous recombination (HR) is dependent on DNA end resection and on post-translational modification of repair factors. In budding yeast, single-stranded DNA is coated by replication protein A (RPA) following DNA end resection, and DNA-RPA complexes are then SUMO-modified by the E3 ligase Siz2 to promote repair. Here, we show using enzymatic assays that DNA duplexes containing 3' single-stranded DNA overhangs increase the rate of RPA SUMO modification by Siz2. The SAP domain of Siz2 binds DNA duplexes and makes a key contribution to this process as highlighted by models and a crystal structure of Siz2 and by assays performed using protein mutants. Enzymatic assays performed using DNA that can accommodate multiple RPA proteins suggest a model in which the SUMO-RPA signal is amplified by successive rounds of Siz2-dependent SUMO modification of RPA and dissociation of SUMO-RPA at the junction between single- and double-stranded DNA. Our results provide insights on how DNA architecture scaffolds a substrate and E3 ligase to promote SUMO modification in the context of DNA repair.
同源重组(HR)修复 DNA 双链断裂依赖于 DNA 末端切除和修复因子的翻译后修饰。在 budding 酵母中,DNA 末端切除后,单链 DNA 被复制蛋白 A(RPA)覆盖,然后 DNA-RPA 复合物被 E3 连接酶 Siz2 进行 SUMO 修饰,以促进修复。在这里,我们使用酶促分析表明,含有 3'单链 DNA 突出端的 DNA 双链体增加了 Siz2 对 RPA SUMO 修饰的速率。Siz2 的 SAP 结构域结合 DNA 双链体,并且通过模型和 Siz2 的晶体结构以及使用蛋白质突变体进行的测定突出显示了这一过程的关键贡献。使用可以容纳多个 RPA 蛋白的 DNA 进行的酶促分析表明,SUMO-RPA 信号通过 Siz2 依赖性 RPA SUMO 修饰的连续轮次以及在单链和双链 DNA 之间的连接处的 SUMO-RPA 解离来放大的模型。我们的结果提供了有关 DNA 结构如何支架底物和 E3 连接酶以促进 DNA 修复背景下 SUMO 修饰的见解。