Margarita Beskrovnaia , Aleksei Agapov , Kristina Makasheva , Dmitry O. Zharkov , Daria Esyunina , Andrey Kulbachinskiy
{"title":"Sensing of DNA modifications by pAgo proteins in vitro","authors":"Margarita Beskrovnaia , Aleksei Agapov , Kristina Makasheva , Dmitry O. Zharkov , Daria Esyunina , Andrey Kulbachinskiy","doi":"10.1016/j.biochi.2023.12.006","DOIUrl":null,"url":null,"abstract":"<div><p><span><span>Many prokaryotic Argonaute<span><span> (pAgo) proteins act as programmable nucleases that use small guide </span>DNAs for recognition and cleavage of complementary target DNA. Recent studies suggested that pAgos participate in cell defense against invader DNA and may also be involved in other </span></span>genetic processes, including DNA replication and repair. The ability of pAgos to recognize specific targets potentially make them an invaluable tool for DNA manipulations. Here, we demonstrate that DNA-guided DNA-targeting pAgo nucleases from three bacterial species, DloAgo from </span><em>Dorea longicatena</em>, CbAgo from <span><em>Clostridium butyricum</em></span> and KmAgo from <em>Kurthia massiliensis</em><span>, can sense site-specific modifications in the target DNA, including 8-oxoguanine, thymine<span> glycol, ethenoadenine and pyrimidine dimers<span>. The effects of DNA modifications<span> on the activity of pAgos strongly depend on their positions relative to the site of cleavage and are comparable to or exceed the effects of guide-target mismatches at corresponding positions. For all tested pAgos, the strongest effects are observed when DNA lesions are located at the cleavage position. The results demonstrate that DNA cleavage by pAgos is strongly affected by DNA modifications, thus making possible their use as sensors of DNA damage.</span></span></span></span></p></div>","PeriodicalId":3,"journal":{"name":"ACS Applied Electronic Materials","volume":null,"pages":null},"PeriodicalIF":4.3000,"publicationDate":"2023-12-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Applied Electronic Materials","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0300908423003309","RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ENGINEERING, ELECTRICAL & ELECTRONIC","Score":null,"Total":0}
引用次数: 0
Abstract
Many prokaryotic Argonaute (pAgo) proteins act as programmable nucleases that use small guide DNAs for recognition and cleavage of complementary target DNA. Recent studies suggested that pAgos participate in cell defense against invader DNA and may also be involved in other genetic processes, including DNA replication and repair. The ability of pAgos to recognize specific targets potentially make them an invaluable tool for DNA manipulations. Here, we demonstrate that DNA-guided DNA-targeting pAgo nucleases from three bacterial species, DloAgo from Dorea longicatena, CbAgo from Clostridium butyricum and KmAgo from Kurthia massiliensis, can sense site-specific modifications in the target DNA, including 8-oxoguanine, thymine glycol, ethenoadenine and pyrimidine dimers. The effects of DNA modifications on the activity of pAgos strongly depend on their positions relative to the site of cleavage and are comparable to or exceed the effects of guide-target mismatches at corresponding positions. For all tested pAgos, the strongest effects are observed when DNA lesions are located at the cleavage position. The results demonstrate that DNA cleavage by pAgos is strongly affected by DNA modifications, thus making possible their use as sensors of DNA damage.
许多原核生物的Argonaute(pAgo)蛋白作为可编程核酸酶,利用小的引导DNA识别和切割互补的目标DNA。最近的研究表明,pAgos 参与细胞对入侵 DNA 的防御,还可能参与其他遗传过程,包括 DNA 复制和修复。pAgos 识别特定目标的能力可能使它们成为 DNA 操作的宝贵工具。在这里,我们证明了来自三个细菌物种的 DNA 引导的 DNA 靶向 pAgo 核酸酶,即来自 Dorea longicatena 的 DloAgo、来自 Clostridium butyricum 的 CbAgo 和来自 Kurthia massiliensis 的 KmAgo,能够感知靶 DNA 中的特定位点修饰,包括 8-氧鸟嘌呤、胸腺嘧啶二醇、乙烯腺嘌呤和嘧啶二聚体。DNA 修饰对 pAgos 活性的影响在很大程度上取决于它们相对于裂解位点的位置,其影响可与相应位置上的指导目标错配相媲美,甚至超过错配的影响。对于所有测试过的 pAgos,当 DNA 损伤位于裂解位置时,观察到的效应最强。结果表明,pAgos 对 DNA 的裂解受到 DNA 修饰的强烈影响,因此可以将其用作 DNA 损伤的传感器。