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Detection of siRNA-mediated target mRNA cleavage activities in human cells by a novel stem-loop array RT-PCR analysis

The small interfering RNA (siRNA)-mediated target mRNA cleavage activity generates cleaved mRNA fragments with varied termini, which creates major technical challenges for the accurate and efficient detection and verification of cleavage sites on target mRNAs. Here we used a sensitive stem-loop arra...

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Detalles Bibliográficos
Autores principales: Lin, Jing, Xu, Kai, Roth, Jack A., Ji, Lin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4776327/
https://www.ncbi.nlm.nih.gov/pubmed/26949742
http://dx.doi.org/10.1016/j.bbrep.2016.02.012
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author Lin, Jing
Xu, Kai
Roth, Jack A.
Ji, Lin
author_facet Lin, Jing
Xu, Kai
Roth, Jack A.
Ji, Lin
author_sort Lin, Jing
collection PubMed
description The small interfering RNA (siRNA)-mediated target mRNA cleavage activity generates cleaved mRNA fragments with varied termini, which creates major technical challenges for the accurate and efficient detection and verification of cleavage sites on target mRNAs. Here we used a sensitive stem-loop array reverse transcription polymerase chain reaction (SLA-RT-PCR) approach to detect and verify the siRNA-mediated target mRNA cleavage sites by determining precise sequences at the 3′- termini of cleaved mRNA fragments in human cells under physiological conditions. Our results demonstrated the great potential and broad applications of using the SLA-RT-PCR as a sensitive, cost-efficient, and high-throughput tool to systematically detect siRNA-targeted mRNA cleavage sites and fragments in human cells.
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spelling pubmed-47763272017-07-01 Detection of siRNA-mediated target mRNA cleavage activities in human cells by a novel stem-loop array RT-PCR analysis Lin, Jing Xu, Kai Roth, Jack A. Ji, Lin Biochem Biophys Rep Research Article The small interfering RNA (siRNA)-mediated target mRNA cleavage activity generates cleaved mRNA fragments with varied termini, which creates major technical challenges for the accurate and efficient detection and verification of cleavage sites on target mRNAs. Here we used a sensitive stem-loop array reverse transcription polymerase chain reaction (SLA-RT-PCR) approach to detect and verify the siRNA-mediated target mRNA cleavage sites by determining precise sequences at the 3′- termini of cleaved mRNA fragments in human cells under physiological conditions. Our results demonstrated the great potential and broad applications of using the SLA-RT-PCR as a sensitive, cost-efficient, and high-throughput tool to systematically detect siRNA-targeted mRNA cleavage sites and fragments in human cells. Elsevier 2016-02-24 /pmc/articles/PMC4776327/ /pubmed/26949742 http://dx.doi.org/10.1016/j.bbrep.2016.02.012 Text en © 2016 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Article
Lin, Jing
Xu, Kai
Roth, Jack A.
Ji, Lin
Detection of siRNA-mediated target mRNA cleavage activities in human cells by a novel stem-loop array RT-PCR analysis
title Detection of siRNA-mediated target mRNA cleavage activities in human cells by a novel stem-loop array RT-PCR analysis
title_full Detection of siRNA-mediated target mRNA cleavage activities in human cells by a novel stem-loop array RT-PCR analysis
title_fullStr Detection of siRNA-mediated target mRNA cleavage activities in human cells by a novel stem-loop array RT-PCR analysis
title_full_unstemmed Detection of siRNA-mediated target mRNA cleavage activities in human cells by a novel stem-loop array RT-PCR analysis
title_short Detection of siRNA-mediated target mRNA cleavage activities in human cells by a novel stem-loop array RT-PCR analysis
title_sort detection of sirna-mediated target mrna cleavage activities in human cells by a novel stem-loop array rt-pcr analysis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4776327/
https://www.ncbi.nlm.nih.gov/pubmed/26949742
http://dx.doi.org/10.1016/j.bbrep.2016.02.012
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