Clemens Steinek, Miguel Guirao-Ortiz, Gabriela Stumberger, Annika J Tölke, David Hörl, Thomas Carell, Hartmann Harz, Heinrich Leonhardt
{"title":"Generation of densely labeled oligonucleotides for the detection of small genomic elements.","authors":"Clemens Steinek, Miguel Guirao-Ortiz, Gabriela Stumberger, Annika J Tölke, David Hörl, Thomas Carell, Hartmann Harz, Heinrich Leonhardt","doi":"10.1016/j.crmeth.2024.100840","DOIUrl":null,"url":null,"abstract":"<p><p>The genome contains numerous regulatory elements that may undergo complex interactions and contribute to the establishment, maintenance, and change of cellular identity. Three-dimensional genome organization can be explored with fluorescence in situ hybridization (FISH) at the single-cell level, but the detection of small genomic loci remains challenging. Here, we provide a rapid and simple protocol for the generation of bright FISH probes suited for the detection of small genomic elements. We systematically optimized probe design and synthesis, screened polymerases for their ability to incorporate dye-labeled nucleotides, and streamlined purification conditions to yield nanoscopy-compatible oligonucleotides with dyes in variable arrays (NOVA probes). With these probes, we detect genomic loci ranging from genome-wide repetitive regions down to non-repetitive loci below the kilobase scale. In conclusion, we introduce a simple workflow to generate densely labeled oligonucleotide pools that facilitate detection and nanoscopic measurements of small genomic elements in single cells.</p>","PeriodicalId":29773,"journal":{"name":"Cell Reports Methods","volume":null,"pages":null},"PeriodicalIF":4.3000,"publicationDate":"2024-08-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11384094/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cell Reports Methods","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1016/j.crmeth.2024.100840","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/8/12 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"BIOCHEMICAL RESEARCH METHODS","Score":null,"Total":0}
引用次数: 0
Abstract
The genome contains numerous regulatory elements that may undergo complex interactions and contribute to the establishment, maintenance, and change of cellular identity. Three-dimensional genome organization can be explored with fluorescence in situ hybridization (FISH) at the single-cell level, but the detection of small genomic loci remains challenging. Here, we provide a rapid and simple protocol for the generation of bright FISH probes suited for the detection of small genomic elements. We systematically optimized probe design and synthesis, screened polymerases for their ability to incorporate dye-labeled nucleotides, and streamlined purification conditions to yield nanoscopy-compatible oligonucleotides with dyes in variable arrays (NOVA probes). With these probes, we detect genomic loci ranging from genome-wide repetitive regions down to non-repetitive loci below the kilobase scale. In conclusion, we introduce a simple workflow to generate densely labeled oligonucleotide pools that facilitate detection and nanoscopic measurements of small genomic elements in single cells.
基因组包含许多调控元件,它们可能会发生复杂的相互作用,并有助于细胞特性的建立、维持和改变。荧光原位杂交(FISH)可在单细胞水平上探索三维基因组的组织结构,但检测小基因组位点仍具有挑战性。在这里,我们提供了一种快速、简单的方案,用于生成适合检测小基因组元件的明亮 FISH 探针。我们对探针的设计和合成进行了系统优化,筛选了聚合酶以确定其结合染料标记的核苷酸的能力,并简化了纯化条件,从而获得了纳米镜兼容的带有可变阵列染料的寡核苷酸(NOVA 探针)。利用这些探针,我们可以检测到从全基因组重复区到千碱基以下非重复位点的基因组位点。总之,我们介绍了一种生成高密度标记寡核苷酸池的简单工作流程,它有助于检测和纳米测量单细胞中的小基因组元素。