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

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.

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Publication Details

Journal
Cell Reports Methods
Published
2024-08-01
DOI
https://doi.org/10.1016/j.crmeth.2024.100840
Citations
7
Primary Topic
Advanced biosensing and bioanalysis techniques
Type
article
Field-Weighted Citation Impact
1.64

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article

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

Hartmann Harz, Thomas Carell, Clemens Steinek, Heinrich Leonhardt et al.
7 citations
Cell Reports Methods
Advanced biosensing and bioanalysis techniques
1.64
article

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

Hartmann Harz, Thomas Carell, Clemens Steinek, Heinrich Leonhardt, Miguel Guirao‐Ortiz, David Hörl, Gabriela Stumberger, Annika J. Tölke
article en
7 citations

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.

Cell Reports MethodsVol. 4(8)
Ludwig-Maximilians-Universität München (DE)
Deutsche Forschungsgemeinschaft, Bundesministerium für Bildung und Forschung, Ludwig-Maximilians-Universität München
Zero hunger
Openalex Percentile: Top 16%
Advanced biosensing and bioanalysis techniques
1.64
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Generation of densely labeled oligonucleotides for the detection of small genomic elements — Hartmann Harz, Thomas Carell, et al. · Cell Reports Methods (2024) | TGRS Research Map | TGRS