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3′LIFE: a functional assay to detect miRNA targets in high-throughput
MicroRNAs (miRNAs) are short non-coding RNAs that regulate gene output at the post-transcriptional level by targeting degenerate elements primarily in 3′untranslated regions (3′UTRs) of mRNAs. Individual miRNAs can regulate networks of hundreds of genes, yet for the majority of miRNAs few, if any, t...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4176154/ https://www.ncbi.nlm.nih.gov/pubmed/25074381 http://dx.doi.org/10.1093/nar/gku626 |
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author | Wolter, Justin M. Kotagama, Kasuen Pierre-Bez, Alexandra C. Firago, Mari Mangone, Marco |
author_facet | Wolter, Justin M. Kotagama, Kasuen Pierre-Bez, Alexandra C. Firago, Mari Mangone, Marco |
author_sort | Wolter, Justin M. |
collection | PubMed |
description | MicroRNAs (miRNAs) are short non-coding RNAs that regulate gene output at the post-transcriptional level by targeting degenerate elements primarily in 3′untranslated regions (3′UTRs) of mRNAs. Individual miRNAs can regulate networks of hundreds of genes, yet for the majority of miRNAs few, if any, targets are known. Misexpression of miRNAs is also a major contributor to cancer progression, thus there is a critical need to validate miRNA targets in high-throughput to understand miRNAs' contribution to tumorigenesis. Here we introduce a novel high-throughput assay to detect miRNA targets in 3′UTRs, called Luminescent Identification of Functional Elements in 3′UTRs (3′LIFE). We demonstrate the feasibility of 3′LIFE using a data set of 275 human 3′UTRs and two cancer-relevant miRNAs, let-7c and miR-10b, and compare our results to alternative methods to detect miRNA targets throughout the genome. We identify a large number of novel gene targets for these miRNAs, with only 32% of hits being bioinformatically predicted and 27% directed by non-canonical interactions. Functional analysis of target genes reveals consistent roles for each miRNA as either a tumor suppressor (let-7c) or oncogenic miRNA (miR-10b), and preferentially target multiple genes within regulatory networks, suggesting 3′LIFE is a rapid and sensitive method to detect miRNA targets in high-throughput. |
format | Online Article Text |
id | pubmed-4176154 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-41761542014-12-01 3′LIFE: a functional assay to detect miRNA targets in high-throughput Wolter, Justin M. Kotagama, Kasuen Pierre-Bez, Alexandra C. Firago, Mari Mangone, Marco Nucleic Acids Res Methods Online MicroRNAs (miRNAs) are short non-coding RNAs that regulate gene output at the post-transcriptional level by targeting degenerate elements primarily in 3′untranslated regions (3′UTRs) of mRNAs. Individual miRNAs can regulate networks of hundreds of genes, yet for the majority of miRNAs few, if any, targets are known. Misexpression of miRNAs is also a major contributor to cancer progression, thus there is a critical need to validate miRNA targets in high-throughput to understand miRNAs' contribution to tumorigenesis. Here we introduce a novel high-throughput assay to detect miRNA targets in 3′UTRs, called Luminescent Identification of Functional Elements in 3′UTRs (3′LIFE). We demonstrate the feasibility of 3′LIFE using a data set of 275 human 3′UTRs and two cancer-relevant miRNAs, let-7c and miR-10b, and compare our results to alternative methods to detect miRNA targets throughout the genome. We identify a large number of novel gene targets for these miRNAs, with only 32% of hits being bioinformatically predicted and 27% directed by non-canonical interactions. Functional analysis of target genes reveals consistent roles for each miRNA as either a tumor suppressor (let-7c) or oncogenic miRNA (miR-10b), and preferentially target multiple genes within regulatory networks, suggesting 3′LIFE is a rapid and sensitive method to detect miRNA targets in high-throughput. Oxford University Press 2014-09-29 2014-07-29 /pmc/articles/PMC4176154/ /pubmed/25074381 http://dx.doi.org/10.1093/nar/gku626 Text en © The Author(s) 2014. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Methods Online Wolter, Justin M. Kotagama, Kasuen Pierre-Bez, Alexandra C. Firago, Mari Mangone, Marco 3′LIFE: a functional assay to detect miRNA targets in high-throughput |
title | 3′LIFE: a functional assay to detect miRNA targets in high-throughput |
title_full | 3′LIFE: a functional assay to detect miRNA targets in high-throughput |
title_fullStr | 3′LIFE: a functional assay to detect miRNA targets in high-throughput |
title_full_unstemmed | 3′LIFE: a functional assay to detect miRNA targets in high-throughput |
title_short | 3′LIFE: a functional assay to detect miRNA targets in high-throughput |
title_sort | 3′life: a functional assay to detect mirna targets in high-throughput |
topic | Methods Online |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4176154/ https://www.ncbi.nlm.nih.gov/pubmed/25074381 http://dx.doi.org/10.1093/nar/gku626 |
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