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Revealing details: whole mount microRNA in situ hybridization protocol for zebrafish embryos and adult tissues

Non-coding microRNA (miRNA) molecules bind their target mRNAs and thereby modulate the amount of protein produced. To understand the significance of a potential miRNA-mRNA interaction, temporal and spatial information on miRNA and mRNA expression is essential. Here, we provide a detailed protocol fo...

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Detalles Bibliográficos
Autores principales: Lagendijk, Anne Karine, Moulton, Jon D., Bakkers, Jeroen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3509442/
https://www.ncbi.nlm.nih.gov/pubmed/23213449
http://dx.doi.org/10.1242/bio.2012810
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author Lagendijk, Anne Karine
Moulton, Jon D.
Bakkers, Jeroen
author_facet Lagendijk, Anne Karine
Moulton, Jon D.
Bakkers, Jeroen
author_sort Lagendijk, Anne Karine
collection PubMed
description Non-coding microRNA (miRNA) molecules bind their target mRNAs and thereby modulate the amount of protein produced. To understand the significance of a potential miRNA-mRNA interaction, temporal and spatial information on miRNA and mRNA expression is essential. Here, we provide a detailed protocol for miRNA whole mount in situ hybridization. We introduce the use of Morpholino based oligos as antisense probes for miRNA detection, in addition to the current “gold standard” locked nucleic acid (LNA) probes. Furthermore we have modified existing miRNA in situ protocols thereby improving both sensitivity and resolution of miRNA visualization in whole zebrafish embryos and adult tissues.
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spelling pubmed-35094422012-12-04 Revealing details: whole mount microRNA in situ hybridization protocol for zebrafish embryos and adult tissues Lagendijk, Anne Karine Moulton, Jon D. Bakkers, Jeroen Biol Open Research Article Non-coding microRNA (miRNA) molecules bind their target mRNAs and thereby modulate the amount of protein produced. To understand the significance of a potential miRNA-mRNA interaction, temporal and spatial information on miRNA and mRNA expression is essential. Here, we provide a detailed protocol for miRNA whole mount in situ hybridization. We introduce the use of Morpholino based oligos as antisense probes for miRNA detection, in addition to the current “gold standard” locked nucleic acid (LNA) probes. Furthermore we have modified existing miRNA in situ protocols thereby improving both sensitivity and resolution of miRNA visualization in whole zebrafish embryos and adult tissues. The Company of Biologists 2012-04-11 /pmc/articles/PMC3509442/ /pubmed/23213449 http://dx.doi.org/10.1242/bio.2012810 Text en © 2012. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by-nc-sa/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial Share Alike License (http://creativecommons.org/licenses/by-nc-sa/3.0/).
spellingShingle Research Article
Lagendijk, Anne Karine
Moulton, Jon D.
Bakkers, Jeroen
Revealing details: whole mount microRNA in situ hybridization protocol for zebrafish embryos and adult tissues
title Revealing details: whole mount microRNA in situ hybridization protocol for zebrafish embryos and adult tissues
title_full Revealing details: whole mount microRNA in situ hybridization protocol for zebrafish embryos and adult tissues
title_fullStr Revealing details: whole mount microRNA in situ hybridization protocol for zebrafish embryos and adult tissues
title_full_unstemmed Revealing details: whole mount microRNA in situ hybridization protocol for zebrafish embryos and adult tissues
title_short Revealing details: whole mount microRNA in situ hybridization protocol for zebrafish embryos and adult tissues
title_sort revealing details: whole mount microrna in situ hybridization protocol for zebrafish embryos and adult tissues
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3509442/
https://www.ncbi.nlm.nih.gov/pubmed/23213449
http://dx.doi.org/10.1242/bio.2012810
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