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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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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2010
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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 |
format | Text |
id | pubmed-2864223 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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