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A Novel Vector-Based Method for Exclusive Overexpression of Star-Form MicroRNAs
The roles of microRNAs (miRNAs) as important regulators of gene expression have been studied intensively. Although most of these investigations have involved the highly expressed form of the two mature miRNA species, increasing evidence points to essential roles for star-form microRNAs (miRNA*), whi...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3400617/ https://www.ncbi.nlm.nih.gov/pubmed/22829954 http://dx.doi.org/10.1371/journal.pone.0041504 |
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author | Qu, Bo Han, Xiao Tang, Yuanjia Shen, Nan |
author_facet | Qu, Bo Han, Xiao Tang, Yuanjia Shen, Nan |
author_sort | Qu, Bo |
collection | PubMed |
description | The roles of microRNAs (miRNAs) as important regulators of gene expression have been studied intensively. Although most of these investigations have involved the highly expressed form of the two mature miRNA species, increasing evidence points to essential roles for star-form microRNAs (miRNA*), which are usually expressed at much lower levels. Owing to the nature of miRNA biogenesis, it is challenging to use plasmids containing miRNA coding sequences for gain-of-function experiments concerning the roles of microRNA* species. Synthetic microRNA mimics could introduce specific miRNA* species into cells, but this transient overexpression system has many shortcomings. Here, we report that specific miRNA* species can be overexpressed by introducing artificially designed stem-loop sequences into short hairpin RNA (shRNA) overexpression vectors. By our prototypic plasmid, designed to overexpress hsa-miR-146b-3p, we successfully expressed high levels of hsa-miR-146b-3p without detectable change of hsa-miR-146b-5p. Functional analysis involving luciferase reporter assays showed that, like natural miRNAs, the overexpressed hsa-miR-146b-3p inhibited target gene expression by 3′UTR seed pairing. Our demonstration that this method could overexpress two other miRNAs suggests that the approach should be broadly applicable. Our novel strategy opens the way for exclusively stable overexpression of miRNA* species and analyzing their unique functions both in vitro and in vivo. |
format | Online Article Text |
id | pubmed-3400617 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-34006172012-07-24 A Novel Vector-Based Method for Exclusive Overexpression of Star-Form MicroRNAs Qu, Bo Han, Xiao Tang, Yuanjia Shen, Nan PLoS One Research Article The roles of microRNAs (miRNAs) as important regulators of gene expression have been studied intensively. Although most of these investigations have involved the highly expressed form of the two mature miRNA species, increasing evidence points to essential roles for star-form microRNAs (miRNA*), which are usually expressed at much lower levels. Owing to the nature of miRNA biogenesis, it is challenging to use plasmids containing miRNA coding sequences for gain-of-function experiments concerning the roles of microRNA* species. Synthetic microRNA mimics could introduce specific miRNA* species into cells, but this transient overexpression system has many shortcomings. Here, we report that specific miRNA* species can be overexpressed by introducing artificially designed stem-loop sequences into short hairpin RNA (shRNA) overexpression vectors. By our prototypic plasmid, designed to overexpress hsa-miR-146b-3p, we successfully expressed high levels of hsa-miR-146b-3p without detectable change of hsa-miR-146b-5p. Functional analysis involving luciferase reporter assays showed that, like natural miRNAs, the overexpressed hsa-miR-146b-3p inhibited target gene expression by 3′UTR seed pairing. Our demonstration that this method could overexpress two other miRNAs suggests that the approach should be broadly applicable. Our novel strategy opens the way for exclusively stable overexpression of miRNA* species and analyzing their unique functions both in vitro and in vivo. Public Library of Science 2012-07-19 /pmc/articles/PMC3400617/ /pubmed/22829954 http://dx.doi.org/10.1371/journal.pone.0041504 Text en Qu et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Qu, Bo Han, Xiao Tang, Yuanjia Shen, Nan A Novel Vector-Based Method for Exclusive Overexpression of Star-Form MicroRNAs |
title | A Novel Vector-Based Method for Exclusive Overexpression of Star-Form MicroRNAs |
title_full | A Novel Vector-Based Method for Exclusive Overexpression of Star-Form MicroRNAs |
title_fullStr | A Novel Vector-Based Method for Exclusive Overexpression of Star-Form MicroRNAs |
title_full_unstemmed | A Novel Vector-Based Method for Exclusive Overexpression of Star-Form MicroRNAs |
title_short | A Novel Vector-Based Method for Exclusive Overexpression of Star-Form MicroRNAs |
title_sort | novel vector-based method for exclusive overexpression of star-form micrornas |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3400617/ https://www.ncbi.nlm.nih.gov/pubmed/22829954 http://dx.doi.org/10.1371/journal.pone.0041504 |
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