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Multiplexed Sequential DNA FISH in Caenorhabditis elegans Embryos

This protocol describes a high-throughput and multiplexed DNA fluorescence in situ hybridization method to trace chromosome conformation in Caenorhabditis elegans embryos. This approach generates single-cell and single-chromosome localization data that can be used to determine chromosome conformatio...

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Autores principales: Sawh, Ahilya N., Mango, Susan E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7756932/
https://www.ncbi.nlm.nih.gov/pubmed/33377003
http://dx.doi.org/10.1016/j.xpro.2020.100107
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author Sawh, Ahilya N.
Mango, Susan E.
author_facet Sawh, Ahilya N.
Mango, Susan E.
author_sort Sawh, Ahilya N.
collection PubMed
description This protocol describes a high-throughput and multiplexed DNA fluorescence in situ hybridization method to trace chromosome conformation in Caenorhabditis elegans embryos. This approach generates single-cell and single-chromosome localization data that can be used to determine chromosome conformation and assess the heterogeneity of structures that exist in vivo. This strategy is flexible through modifications to the probe design steps to interrogate chromosome structure at the desired genomic scale (small-scale loops to whole-chromosome organization). For complete details on the use and execution of this protocol, please refer to Sawh et al. (2020).
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spelling pubmed-77569322020-12-28 Multiplexed Sequential DNA FISH in Caenorhabditis elegans Embryos Sawh, Ahilya N. Mango, Susan E. STAR Protoc Protocol This protocol describes a high-throughput and multiplexed DNA fluorescence in situ hybridization method to trace chromosome conformation in Caenorhabditis elegans embryos. This approach generates single-cell and single-chromosome localization data that can be used to determine chromosome conformation and assess the heterogeneity of structures that exist in vivo. This strategy is flexible through modifications to the probe design steps to interrogate chromosome structure at the desired genomic scale (small-scale loops to whole-chromosome organization). For complete details on the use and execution of this protocol, please refer to Sawh et al. (2020). Elsevier 2020-09-09 /pmc/articles/PMC7756932/ /pubmed/33377003 http://dx.doi.org/10.1016/j.xpro.2020.100107 Text en © 2020. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Protocol
Sawh, Ahilya N.
Mango, Susan E.
Multiplexed Sequential DNA FISH in Caenorhabditis elegans Embryos
title Multiplexed Sequential DNA FISH in Caenorhabditis elegans Embryos
title_full Multiplexed Sequential DNA FISH in Caenorhabditis elegans Embryos
title_fullStr Multiplexed Sequential DNA FISH in Caenorhabditis elegans Embryos
title_full_unstemmed Multiplexed Sequential DNA FISH in Caenorhabditis elegans Embryos
title_short Multiplexed Sequential DNA FISH in Caenorhabditis elegans Embryos
title_sort multiplexed sequential dna fish in caenorhabditis elegans embryos
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7756932/
https://www.ncbi.nlm.nih.gov/pubmed/33377003
http://dx.doi.org/10.1016/j.xpro.2020.100107
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