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Inhibiting miRNA in Caenorhabditis elegans using a potent and selective antisense reagent

BACKGROUND: Antisense reagents can serve as efficient and versatile tools for studying gene function by inhibiting nucleic acids in vivo. Antisense reagents have particular utility for the experimental manipulation of the activity of microRNAs (miRNAs), which are involved in the regulation of divers...

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Autores principales: Zheng, Genhua, Ambros, Victor, Li, Wen-hong
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2864223/
https://www.ncbi.nlm.nih.gov/pubmed/20359322
http://dx.doi.org/10.1186/1758-907X-1-9
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author Zheng, Genhua
Ambros, Victor
Li, Wen-hong
author_facet Zheng, Genhua
Ambros, Victor
Li, Wen-hong
author_sort Zheng, Genhua
collection PubMed
description BACKGROUND: Antisense reagents can serve as efficient and versatile tools for studying gene function by inhibiting nucleic acids in vivo. Antisense reagents have particular utility for the experimental manipulation of the activity of microRNAs (miRNAs), which are involved in the regulation of diverse developmental and physiological pathways in animals. Even in traditional genetic systems, such as the nematode Caenorhabditis elegans, antisense reagents can provide experimental strategies complementary to mutational approaches. Presently no antisense reagents are available for inhibiting miRNAs in the nematode C. elegans. RESULTS: We have developed a new class of fluorescently labelled antisense reagents to inhibit miRNAs in developing worms. These reagents were synthesized by conjugating dextran with 2'-O-methyl oligoribonucleotide. The dextran-conjugated antisense reagents can be conveniently introduced into the germline of adult hermaphrodites and are transmitted to their progeny, where they efficiently and specifically inhibit a targeted miRNA in different tissues, including the hypodermis, the vulva and the nervous system. We show that these reagents can be used combinatorially to inhibit more than one miRNA in the same animal. CONCLUSION: This class of antisense reagents represents a new addition to the toolkit for studying miRNA in C. elegans. Combined with numerous mutants or reporter stains available, these reagents should provide a convenient approach to examine genetic interactions that involve miRNA, and may facilitate studying functions of miRNAs, especially ones whose deletion strains are difficult to generate. See related research article: http://jbiol.com/content/9/3/20
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spelling pubmed-28642232010-05-05 Inhibiting miRNA in Caenorhabditis elegans using a potent and selective antisense reagent Zheng, Genhua Ambros, Victor Li, Wen-hong Silence Methodology BACKGROUND: Antisense reagents can serve as efficient and versatile tools for studying gene function by inhibiting nucleic acids in vivo. Antisense reagents have particular utility for the experimental manipulation of the activity of microRNAs (miRNAs), which are involved in the regulation of diverse developmental and physiological pathways in animals. Even in traditional genetic systems, such as the nematode Caenorhabditis elegans, antisense reagents can provide experimental strategies complementary to mutational approaches. Presently no antisense reagents are available for inhibiting miRNAs in the nematode C. elegans. RESULTS: We have developed a new class of fluorescently labelled antisense reagents to inhibit miRNAs in developing worms. These reagents were synthesized by conjugating dextran with 2'-O-methyl oligoribonucleotide. The dextran-conjugated antisense reagents can be conveniently introduced into the germline of adult hermaphrodites and are transmitted to their progeny, where they efficiently and specifically inhibit a targeted miRNA in different tissues, including the hypodermis, the vulva and the nervous system. We show that these reagents can be used combinatorially to inhibit more than one miRNA in the same animal. CONCLUSION: This class of antisense reagents represents a new addition to the toolkit for studying miRNA in C. elegans. Combined with numerous mutants or reporter stains available, these reagents should provide a convenient approach to examine genetic interactions that involve miRNA, and may facilitate studying functions of miRNAs, especially ones whose deletion strains are difficult to generate. See related research article: http://jbiol.com/content/9/3/20 BioMed Central 2010-04-01 /pmc/articles/PMC2864223/ /pubmed/20359322 http://dx.doi.org/10.1186/1758-907X-1-9 Text en Copyright ©2010 Zheng et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Methodology
Zheng, Genhua
Ambros, Victor
Li, Wen-hong
Inhibiting miRNA in Caenorhabditis elegans using a potent and selective antisense reagent
title Inhibiting miRNA in Caenorhabditis elegans using a potent and selective antisense reagent
title_full Inhibiting miRNA in Caenorhabditis elegans using a potent and selective antisense reagent
title_fullStr Inhibiting miRNA in Caenorhabditis elegans using a potent and selective antisense reagent
title_full_unstemmed Inhibiting miRNA in Caenorhabditis elegans using a potent and selective antisense reagent
title_short Inhibiting miRNA in Caenorhabditis elegans using a potent and selective antisense reagent
title_sort inhibiting mirna in caenorhabditis elegans using a potent and selective antisense reagent
topic Methodology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2864223/
https://www.ncbi.nlm.nih.gov/pubmed/20359322
http://dx.doi.org/10.1186/1758-907X-1-9
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