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生成用于检测小基因组元件的高密度标记寡核苷酸。

Generation of densely labeled oligonucleotides for the detection of small genomic elements.

机构信息

Faculty of Biology and Center for Molecular Biosystems (BioSysM), Human Biology and BioImaging, Ludwig-Maximilians-Universität München, 81377 Munich, Germany.

Faculty of Biology and Center for Molecular Biosystems (BioSysM), Human Biology and BioImaging, Ludwig-Maximilians-Universität München, 81377 Munich, Germany.

出版信息

Cell Rep Methods. 2024 Aug 19;4(8):100840. doi: 10.1016/j.crmeth.2024.100840. Epub 2024 Aug 12.

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.

摘要

基因组包含许多调控元件,这些元件可能发生复杂的相互作用,并有助于细胞身份的建立、维持和改变。在单细胞水平上,可以通过荧光原位杂交(FISH)来探索三维基因组结构,但对小基因组区域的检测仍然具有挑战性。在这里,我们提供了一种快速而简单的方法来生成适合检测小基因组元件的明亮 FISH 探针。我们系统地优化了探针设计和合成,筛选了能够掺入染料标记核苷酸的聚合酶,并简化了纯化条件,以产生带有不同阵列染料的适用于纳米显微镜的寡核苷酸(NOVA 探针)。利用这些探针,我们可以检测从全基因组重复区域到千碱基以下非重复区域的基因组位点。总之,我们引入了一种简单的工作流程来生成密集标记的寡核苷酸池,这有助于在单细胞中检测和纳米级测量小基因组元件。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c0c/11384094/5a57f12153a2/fx1.jpg

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