Please use this identifier to cite or link to this item: http://doi.org/10.25358/openscience-243
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dc.contributor.authorOnchuru, Thomas-
dc.contributor.authorKaltenpoth, Martin-
dc.date.accessioned2019-12-16T09:48:32Z-
dc.date.available2019-12-16T10:48:32Z-
dc.date.issued2019-
dc.identifier.urihttps://openscience.ub.uni-mainz.de/handle/20.500.12030/245-
dc.description.abstractRNA interference (RNAi) is a powerful tool for studying functions of candidate genes in both model and nonmodel organisms and a promising technique for therapeutic applications. Successful application of this technique relies on the accuracy and reliability of methods used to quantify gene knockdown. With the limitation in the availability of antibodies for detecting proteins, quantitative PCR (qPCR) remains the preferred method for quantifying target gene knockdown after dsRNA treatment. We evaluated how qPCR primer binding site and target gene expression levels affect quantification of intact mRNA transcripts following dsRNA-mediated RNAi. The use of primer pairs targeting the mRNA sequence within the dsRNA target region failed to reveal a significant decrease in target mRNA transcripts for genes with low expression levels, but not for a highly expressed gene. By contrast, significant knockdown was detected in all cases with primer pairs targeting the mRNA sequence extending beyond the dsRNA target region, regardless of the expression levels of the target gene. Our results suggest that at least for genes with low expression levels, quantifying the efficiency of dsRNA-mediated RNAi with primers amplifying sequences completely contained in the dsRNA target region should be avoided due to the risk of false-negative results. Instead, primer pairs extending beyond the dsRNA target region of the mRNA transcript sequences should be used for accurate and reliable quantification of silencing efficiency.en_GB
dc.description.sponsorshipDFG, Open Access-Publizieren Universität Mainz / Universitätsmedizin-
dc.language.isoeng-
dc.rightsCC BYde_DE
dc.rights.urihhttps://creativecommons.org/licenses/by/4.0/-
dc.subject.ddc570 Biowissenschaftende_DE
dc.subject.ddc570 Life sciencesen_GB
dc.titleQuantitative PCR primer design affects quantification of dsRNA-mediated gene knockdownen_GB
dc.typeZeitschriftenaufsatzde_DE
dc.identifier.urnurn:nbn:de:hebis:77-publ-594768-
dc.identifier.doihttp://doi.org/10.25358/openscience-243-
jgu.type.dinitypearticle-
jgu.type.versionPublished versionen_GB
jgu.type.resourceText-
jgu.organisation.departmentFB 10 Biologie-
jgu.organisation.number7970-
jgu.organisation.nameJohannes Gutenberg-Universität Mainz-
jgu.rights.accessrightsopenAccess-
jgu.journal.titleEcology and evolution-
jgu.journal.volume9-
jgu.journal.issue14-
jgu.pages.start8187-
jgu.pages.end8192-
jgu.publisher.year2019-
jgu.publisher.nameJohn Wiley & Sons, Inc.-
jgu.publisher.placeS.l.-
jgu.publisher.urihttp://dx.doi.org/10.1002/ece3.5387-
jgu.publisher.issn2045-7758-
jgu.organisation.placeMainz-
jgu.subject.ddccode570-
opus.date.accessioned2019-12-16T09:48:32Z-
opus.date.modified2019-12-16T10:45:28Z-
opus.date.available2019-12-16T10:48:32-
opus.subject.dfgcode00-000-
opus.organisation.stringFB 10: Biologie: Institut für Organismische und Molekulare Evolutionsbiologiede_DE
opus.identifier.opusid59476-
opus.institute.number1011-
opus.metadataonlyfalse-
opus.type.contenttypeKeinede_DE
opus.type.contenttypeNoneen_GB
opus.affiliatedOnchuru, Thomas-
opus.affiliatedKaltenpoth, Martin-
jgu.publisher.doi10.1002/ece3.5387
jgu.organisation.rorhttps://ror.org/023b0x485
Appears in collections:JGU-Publikationen

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