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Rapid and Efficient FISH using Pre-Labeled Oligomer Probes
Fluorescence in situ hybridization (FISH) is used to visualize the distribution of DNA elements within a genome. Conventional methods for FISH take 1–2 days. Here, we developed a simplified, rapid FISH technique using pre-labeled oligonucleotide probes (PLOPs) and tested the procedure using 18 PLOPs...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5974128/ https://www.ncbi.nlm.nih.gov/pubmed/29844509 http://dx.doi.org/10.1038/s41598-018-26667-z |
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author | Waminal, Nomar Espinosa Pellerin, Remnyl Joyce Kim, Nam-Soo Jayakodi, Murukarthick Park, Jee Young Yang, Tae-Jin Kim, Hyun Hee |
author_facet | Waminal, Nomar Espinosa Pellerin, Remnyl Joyce Kim, Nam-Soo Jayakodi, Murukarthick Park, Jee Young Yang, Tae-Jin Kim, Hyun Hee |
author_sort | Waminal, Nomar Espinosa |
collection | PubMed |
description | Fluorescence in situ hybridization (FISH) is used to visualize the distribution of DNA elements within a genome. Conventional methods for FISH take 1–2 days. Here, we developed a simplified, rapid FISH technique using pre-labeled oligonucleotide probes (PLOPs) and tested the procedure using 18 PLOPs from 45S and 5S rDNA, Arabidopsis-type telomere, and newly-identified Panax ginseng-specific tandem repeats. The 16 developed rDNA PLOPs can be universally applied to plants and animals. The telomere PLOPs can be utilized in most plants with Arabidopsis-type telomeres. The ginseng-specific PLOP can be used to distinguish P. ginseng from related Panax species. Differential labeling of PLOPs allowed us to simultaneously visualize different target loci while reducing the FISH hybridization time from ~16 h to 5 min. PLOP-FISH is efficient, reliable, and rapid, making it ideal for routine analysis, especially of newly sequenced genomes using either universal or specific targets, such as novel tandem repeats identified from whole-genome sequencing data. |
format | Online Article Text |
id | pubmed-5974128 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-59741282018-05-31 Rapid and Efficient FISH using Pre-Labeled Oligomer Probes Waminal, Nomar Espinosa Pellerin, Remnyl Joyce Kim, Nam-Soo Jayakodi, Murukarthick Park, Jee Young Yang, Tae-Jin Kim, Hyun Hee Sci Rep Article Fluorescence in situ hybridization (FISH) is used to visualize the distribution of DNA elements within a genome. Conventional methods for FISH take 1–2 days. Here, we developed a simplified, rapid FISH technique using pre-labeled oligonucleotide probes (PLOPs) and tested the procedure using 18 PLOPs from 45S and 5S rDNA, Arabidopsis-type telomere, and newly-identified Panax ginseng-specific tandem repeats. The 16 developed rDNA PLOPs can be universally applied to plants and animals. The telomere PLOPs can be utilized in most plants with Arabidopsis-type telomeres. The ginseng-specific PLOP can be used to distinguish P. ginseng from related Panax species. Differential labeling of PLOPs allowed us to simultaneously visualize different target loci while reducing the FISH hybridization time from ~16 h to 5 min. PLOP-FISH is efficient, reliable, and rapid, making it ideal for routine analysis, especially of newly sequenced genomes using either universal or specific targets, such as novel tandem repeats identified from whole-genome sequencing data. Nature Publishing Group UK 2018-05-29 /pmc/articles/PMC5974128/ /pubmed/29844509 http://dx.doi.org/10.1038/s41598-018-26667-z Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Waminal, Nomar Espinosa Pellerin, Remnyl Joyce Kim, Nam-Soo Jayakodi, Murukarthick Park, Jee Young Yang, Tae-Jin Kim, Hyun Hee Rapid and Efficient FISH using Pre-Labeled Oligomer Probes |
title | Rapid and Efficient FISH using Pre-Labeled Oligomer Probes |
title_full | Rapid and Efficient FISH using Pre-Labeled Oligomer Probes |
title_fullStr | Rapid and Efficient FISH using Pre-Labeled Oligomer Probes |
title_full_unstemmed | Rapid and Efficient FISH using Pre-Labeled Oligomer Probes |
title_short | Rapid and Efficient FISH using Pre-Labeled Oligomer Probes |
title_sort | rapid and efficient fish using pre-labeled oligomer probes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5974128/ https://www.ncbi.nlm.nih.gov/pubmed/29844509 http://dx.doi.org/10.1038/s41598-018-26667-z |
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