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Disease-Causing Allele-Specific Silencing by RNA Interference

Small double-stranded RNAs (dsRNAs) of approximately 21-nucleotides in size, referred to as small interfering RNA (siRNA) duplexes, can induce sequence-specific posttranscriptional gene silencing, or RNA interference (RNAi). Since chemically synthesized siRNA duplexes were found to induce RNAi in ma...

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Detalles Bibliográficos
Autor principal: Hohjoh, Hirohiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3816697/
https://www.ncbi.nlm.nih.gov/pubmed/24276122
http://dx.doi.org/10.3390/ph6040522
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author Hohjoh, Hirohiko
author_facet Hohjoh, Hirohiko
author_sort Hohjoh, Hirohiko
collection PubMed
description Small double-stranded RNAs (dsRNAs) of approximately 21-nucleotides in size, referred to as small interfering RNA (siRNA) duplexes, can induce sequence-specific posttranscriptional gene silencing, or RNA interference (RNAi). Since chemically synthesized siRNA duplexes were found to induce RNAi in mammalian cells, RNAi has become a powerful reverse genetic tool for suppressing the expression of a gene of interest in mammals, including human, and its application has been expanding to various fields. Recent studies further suggest that synthetic siRNA duplexes have the potential for specifically inhibiting the expression of an allele of interest without suppressing the expression of other alleles, i.e., siRNA duplexes likely confer allele-specific silencing. Such gene silencing by RNAi is an advanced technique with very promising applications. In this review, I would like to discuss the potential utility of allele-specific silencing by RNAi as a therapeutic method for dominantly inherited diseases, and describe possible improvements in siRNA duplexes for enhancing their efficacy.
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spelling pubmed-38166972013-11-14 Disease-Causing Allele-Specific Silencing by RNA Interference Hohjoh, Hirohiko Pharmaceuticals (Basel) Review Small double-stranded RNAs (dsRNAs) of approximately 21-nucleotides in size, referred to as small interfering RNA (siRNA) duplexes, can induce sequence-specific posttranscriptional gene silencing, or RNA interference (RNAi). Since chemically synthesized siRNA duplexes were found to induce RNAi in mammalian cells, RNAi has become a powerful reverse genetic tool for suppressing the expression of a gene of interest in mammals, including human, and its application has been expanding to various fields. Recent studies further suggest that synthetic siRNA duplexes have the potential for specifically inhibiting the expression of an allele of interest without suppressing the expression of other alleles, i.e., siRNA duplexes likely confer allele-specific silencing. Such gene silencing by RNAi is an advanced technique with very promising applications. In this review, I would like to discuss the potential utility of allele-specific silencing by RNAi as a therapeutic method for dominantly inherited diseases, and describe possible improvements in siRNA duplexes for enhancing their efficacy. MDPI 2013-04-11 /pmc/articles/PMC3816697/ /pubmed/24276122 http://dx.doi.org/10.3390/ph6040522 Text en © 2013 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0/ This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Review
Hohjoh, Hirohiko
Disease-Causing Allele-Specific Silencing by RNA Interference
title Disease-Causing Allele-Specific Silencing by RNA Interference
title_full Disease-Causing Allele-Specific Silencing by RNA Interference
title_fullStr Disease-Causing Allele-Specific Silencing by RNA Interference
title_full_unstemmed Disease-Causing Allele-Specific Silencing by RNA Interference
title_short Disease-Causing Allele-Specific Silencing by RNA Interference
title_sort disease-causing allele-specific silencing by rna interference
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3816697/
https://www.ncbi.nlm.nih.gov/pubmed/24276122
http://dx.doi.org/10.3390/ph6040522
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