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

CP: Genetics CP: Imaging DNA FISH FISH NOVA-FISH STED microscopy fluorescence in situ hybridization labeling oligomers

Journal

Cell reports methods
ISSN: 2667-2375
Titre abrégé: Cell Rep Methods
Pays: United States
ID NLM: 9918227360606676

Informations de publication

Date de publication:
05 Aug 2024
Historique:
received: 12 03 2024
revised: 16 06 2024
accepted: 22 07 2024
medline: 14 8 2024
pubmed: 14 8 2024
entrez: 13 8 2024
Statut: aheadofprint

Résumé

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.

Identifiants

pubmed: 39137784
pii: S2667-2375(24)00213-3
doi: 10.1016/j.crmeth.2024.100840
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

100840

Informations de copyright

Copyright © 2024 The Author(s). Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of interests The authors declare no competing interests.

Auteurs

Clemens Steinek (C)

Faculty of Biology and Center for Molecular Biosystems (BioSysM), Human Biology and BioImaging, Ludwig-Maximilians-Universität München, 81377 Munich, Germany. Electronic address: steinek@biologie.uni-muenchen.de.

Miguel Guirao-Ortiz (M)

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

Gabriela Stumberger (G)

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

Annika J Tölke (AJ)

Department of Chemistry, Ludwig-Maximilians-Universität München, 81377 Munich, Germany.

David Hörl (D)

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

Thomas Carell (T)

Department of Chemistry, Ludwig-Maximilians-Universität München, 81377 Munich, Germany.

Hartmann Harz (H)

Faculty of Biology and Center for Molecular Biosystems (BioSysM), Human Biology and BioImaging, Ludwig-Maximilians-Universität München, 81377 Munich, Germany. Electronic address: harz@biologie.uni-muenchen.de.

Heinrich Leonhardt (H)

Faculty of Biology and Center for Molecular Biosystems (BioSysM), Human Biology and BioImaging, Ludwig-Maximilians-Universität München, 81377 Munich, Germany. Electronic address: h.leonhardt@lmu.de.

Classifications MeSH