{"title":"Assessment of DNA fibers to track replication dynamics.","authors":"L G Bennett, C J Staples","doi":"10.1016/bs.mcb.2023.02.007","DOIUrl":null,"url":null,"abstract":"<p><p>DNA replication is a complex and tightly regulated process that must proceed accurately and completely if the cell is to faithfully transmit genetic material to its progeny. Organisms have thus evolved complex mechanisms to deal with the myriad exogenous and endogenous sources of replication impediments to which the cell is subject. These mechanisms are of particular relevance to cancer biology, given that such \"replication stress\" frequently foreshadows genome instability during cancer pathogenesis, and that many traditional chemotherapies and a number of precision medicines function by interfering with the progress of DNA replication. Visualization of the progress and dynamics of DNA replication in living cells was historically a major challenge, neatly surmounted by the development of DNA fiber assays that utilize the fluorescent detection of halogenated nucleotides to track replication forks at single-molecule resolution. This methodology has been widely applied to study the dynamics of unperturbed DNA replication, as well as the cellular responses to various replication stress scenarios. In recent years, subtle modifications to DNA fiber assays have facilitated assessment of the stability of nascent DNA at stalled replication forks, as well as the detection of single-stranded DNA gaps and their subsequent filling by error-prone polymerases. Here, we present and discuss several iterations of the fiber assay and suggest methodologies for the analysis of the data obtained.</p>","PeriodicalId":18437,"journal":{"name":"Methods in cell biology","volume":"182 ","pages":"285-298"},"PeriodicalIF":0.0000,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Methods in cell biology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1016/bs.mcb.2023.02.007","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2023/3/30 0:00:00","PubModel":"Epub","JCR":"Q4","JCRName":"Biochemistry, Genetics and Molecular Biology","Score":null,"Total":0}
引用次数: 0
Abstract
DNA replication is a complex and tightly regulated process that must proceed accurately and completely if the cell is to faithfully transmit genetic material to its progeny. Organisms have thus evolved complex mechanisms to deal with the myriad exogenous and endogenous sources of replication impediments to which the cell is subject. These mechanisms are of particular relevance to cancer biology, given that such "replication stress" frequently foreshadows genome instability during cancer pathogenesis, and that many traditional chemotherapies and a number of precision medicines function by interfering with the progress of DNA replication. Visualization of the progress and dynamics of DNA replication in living cells was historically a major challenge, neatly surmounted by the development of DNA fiber assays that utilize the fluorescent detection of halogenated nucleotides to track replication forks at single-molecule resolution. This methodology has been widely applied to study the dynamics of unperturbed DNA replication, as well as the cellular responses to various replication stress scenarios. In recent years, subtle modifications to DNA fiber assays have facilitated assessment of the stability of nascent DNA at stalled replication forks, as well as the detection of single-stranded DNA gaps and their subsequent filling by error-prone polymerases. Here, we present and discuss several iterations of the fiber assay and suggest methodologies for the analysis of the data obtained.
DNA 复制是一个复杂而又受到严格调控的过程,如果细胞要将遗传物质忠实地传递给后代,就必须准确而完整地进行复制。因此,生物体进化出了复杂的机制,以应对细胞所面临的无数外源和内源复制障碍。这些机制与癌症生物学尤为相关,因为在癌症发病过程中,这种 "复制压力 "往往预示着基因组的不稳定性,而且许多传统化疗方法和一些精准药物都是通过干扰 DNA 复制过程来发挥作用的。可视化活细胞中 DNA 复制的进展和动态历来是一项重大挑战,而 DNA 纤维测定法的开发则巧妙地克服了这一挑战,该测定法利用卤代核苷酸的荧光检测,以单分子分辨率跟踪复制叉。这种方法已被广泛应用于研究未受干扰的 DNA 复制动态,以及细胞对各种复制压力情景的反应。近年来,对 DNA 纤维测定法的细微修改促进了对停滞复制叉上新生 DNA 稳定性的评估,以及对单链 DNA 间隙及其随后由易出错的聚合酶填补的检测。在此,我们介绍并讨论了纤维测定的几次迭代,并提出了分析所获数据的方法。
期刊介绍:
For over fifty years, Methods in Cell Biology has helped researchers answer the question "What method should I use to study this cell biology problem?" Edited by leaders in the field, each thematic volume provides proven, state-of-art techniques, along with relevant historical background and theory, to aid researchers in efficient design and effective implementation of experimental methodologies. Over its many years of publication, Methods in Cell Biology has built up a deep library of biological methods to study model developmental organisms, organelles and cell systems, as well as comprehensive coverage of microscopy and other analytical approaches.