Cargando…

Tigerfish designs oligonucleotide-based in situ hybridization probes targeting intervals of highly repetitive DNA at the scale of genomes

Fluorescent in situ hybridization (FISH) is a powerful method for the targeted visualization of nucleic acids in their native contexts. Recent technological advances have leveraged computationally designed oligonucleotide (oligo) probes to interrogate >100 distinct targets in the same sample, pus...

Descripción completa

Detalles Bibliográficos
Autores principales: Aguilar, Robin, Camplisson, Conor K., Lin, Qiaoyi, Miga, Karen H., Noble, William S., Beliveau, Brian J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10028787/
https://www.ncbi.nlm.nih.gov/pubmed/36945528
http://dx.doi.org/10.1101/2023.03.06.530899
_version_ 1784910021744656384
author Aguilar, Robin
Camplisson, Conor K.
Lin, Qiaoyi
Miga, Karen H.
Noble, William S.
Beliveau, Brian J.
author_facet Aguilar, Robin
Camplisson, Conor K.
Lin, Qiaoyi
Miga, Karen H.
Noble, William S.
Beliveau, Brian J.
author_sort Aguilar, Robin
collection PubMed
description Fluorescent in situ hybridization (FISH) is a powerful method for the targeted visualization of nucleic acids in their native contexts. Recent technological advances have leveraged computationally designed oligonucleotide (oligo) probes to interrogate >100 distinct targets in the same sample, pushing the boundaries of FISH-based assays. However, even in the most highly multiplexed experiments, repetitive DNA regions are typically not included as targets, as the computational design of specific probes against such regions presents significant technical challenges. Consequently, many open questions remain about the organization and function of highly repetitive sequences. Here, we introduce Tigerfish, a software tool for the genome-scale design of oligo probes against repetitive DNA intervals. We showcase Tigerfish by designing a panel of 24 interval-specific repeat probes specific to each of the 24 human chromosomes and imaging this panel on metaphase spreads and in interphase nuclei. Tigerfish extends the powerful toolkit of oligo-based FISH to highly repetitive DNA.
format Online
Article
Text
id pubmed-10028787
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Cold Spring Harbor Laboratory
record_format MEDLINE/PubMed
spelling pubmed-100287872023-03-22 Tigerfish designs oligonucleotide-based in situ hybridization probes targeting intervals of highly repetitive DNA at the scale of genomes Aguilar, Robin Camplisson, Conor K. Lin, Qiaoyi Miga, Karen H. Noble, William S. Beliveau, Brian J. bioRxiv Article Fluorescent in situ hybridization (FISH) is a powerful method for the targeted visualization of nucleic acids in their native contexts. Recent technological advances have leveraged computationally designed oligonucleotide (oligo) probes to interrogate >100 distinct targets in the same sample, pushing the boundaries of FISH-based assays. However, even in the most highly multiplexed experiments, repetitive DNA regions are typically not included as targets, as the computational design of specific probes against such regions presents significant technical challenges. Consequently, many open questions remain about the organization and function of highly repetitive sequences. Here, we introduce Tigerfish, a software tool for the genome-scale design of oligo probes against repetitive DNA intervals. We showcase Tigerfish by designing a panel of 24 interval-specific repeat probes specific to each of the 24 human chromosomes and imaging this panel on metaphase spreads and in interphase nuclei. Tigerfish extends the powerful toolkit of oligo-based FISH to highly repetitive DNA. Cold Spring Harbor Laboratory 2023-03-07 /pmc/articles/PMC10028787/ /pubmed/36945528 http://dx.doi.org/10.1101/2023.03.06.530899 Text en https://creativecommons.org/licenses/by-nc/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License (https://creativecommons.org/licenses/by-nc/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format for noncommercial purposes only, and only so long as attribution is given to the creator.
spellingShingle Article
Aguilar, Robin
Camplisson, Conor K.
Lin, Qiaoyi
Miga, Karen H.
Noble, William S.
Beliveau, Brian J.
Tigerfish designs oligonucleotide-based in situ hybridization probes targeting intervals of highly repetitive DNA at the scale of genomes
title Tigerfish designs oligonucleotide-based in situ hybridization probes targeting intervals of highly repetitive DNA at the scale of genomes
title_full Tigerfish designs oligonucleotide-based in situ hybridization probes targeting intervals of highly repetitive DNA at the scale of genomes
title_fullStr Tigerfish designs oligonucleotide-based in situ hybridization probes targeting intervals of highly repetitive DNA at the scale of genomes
title_full_unstemmed Tigerfish designs oligonucleotide-based in situ hybridization probes targeting intervals of highly repetitive DNA at the scale of genomes
title_short Tigerfish designs oligonucleotide-based in situ hybridization probes targeting intervals of highly repetitive DNA at the scale of genomes
title_sort tigerfish designs oligonucleotide-based in situ hybridization probes targeting intervals of highly repetitive dna at the scale of genomes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10028787/
https://www.ncbi.nlm.nih.gov/pubmed/36945528
http://dx.doi.org/10.1101/2023.03.06.530899
work_keys_str_mv AT aguilarrobin tigerfishdesignsoligonucleotidebasedinsituhybridizationprobestargetingintervalsofhighlyrepetitivednaatthescaleofgenomes
AT camplissonconork tigerfishdesignsoligonucleotidebasedinsituhybridizationprobestargetingintervalsofhighlyrepetitivednaatthescaleofgenomes
AT linqiaoyi tigerfishdesignsoligonucleotidebasedinsituhybridizationprobestargetingintervalsofhighlyrepetitivednaatthescaleofgenomes
AT migakarenh tigerfishdesignsoligonucleotidebasedinsituhybridizationprobestargetingintervalsofhighlyrepetitivednaatthescaleofgenomes
AT noblewilliams tigerfishdesignsoligonucleotidebasedinsituhybridizationprobestargetingintervalsofhighlyrepetitivednaatthescaleofgenomes
AT beliveaubrianj tigerfishdesignsoligonucleotidebasedinsituhybridizationprobestargetingintervalsofhighlyrepetitivednaatthescaleofgenomes