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  • Genomic DNA (gDNA) contamination is an inherent problem during RNA purification that can lead to non-specific amplification and aberrant results in reverse transcription quantitative PCR (RT-qPCR). Currently, there is no alternative to RT(-) controls to evaluate the impact of the gDNA background on RT-PCR data. We propose a novel method (ValidPrime) that is more accurate than traditional RT(-) controls to test qPCR assays with respect to their sensitivity toward gDNA. ValidPrime measures the gDNA contribution using an optimized gDNA-specific ValidPrime assay (VPA) and gDNA reference sample(s). The VPA, targeting a nontranscribed locus, is used to measure the gDNA contents in RT(+) samples and the gDNA reference is used to normalize for GOI-specific differences in gDNA sensitivity. We demonstrate that the RNA-derived component of the signal can be accurately estimated and deduced from the total signal. ValidPrime corrects with high precision for both exogenous (spiked) and endogenous gDNA, contributing similar to 60% of the total signal, whereas substantially reducing the number of required qPCR control reactions. In conclusion, ValidPrime offers a cost-efficient alternative to RT(-) controls and accurately corrects for signals derived from gDNA in RT-qPCR.
  • Genomic DNA (gDNA) contamination is an inherent problem during RNA purification that can lead to non-specific amplification and aberrant results in reverse transcription quantitative PCR (RT-qPCR). Currently, there is no alternative to RT(-) controls to evaluate the impact of the gDNA background on RT-PCR data. We propose a novel method (ValidPrime) that is more accurate than traditional RT(-) controls to test qPCR assays with respect to their sensitivity toward gDNA. ValidPrime measures the gDNA contribution using an optimized gDNA-specific ValidPrime assay (VPA) and gDNA reference sample(s). The VPA, targeting a nontranscribed locus, is used to measure the gDNA contents in RT(+) samples and the gDNA reference is used to normalize for GOI-specific differences in gDNA sensitivity. We demonstrate that the RNA-derived component of the signal can be accurately estimated and deduced from the total signal. ValidPrime corrects with high precision for both exogenous (spiked) and endogenous gDNA, contributing similar to 60% of the total signal, whereas substantially reducing the number of required qPCR control reactions. In conclusion, ValidPrime offers a cost-efficient alternative to RT(-) controls and accurately corrects for signals derived from gDNA in RT-qPCR. (en)
Title
  • Correction of RT-qPCR data for genomic DNA-derived signals with ValidPrime
  • Correction of RT-qPCR data for genomic DNA-derived signals with ValidPrime (en)
skos:prefLabel
  • Correction of RT-qPCR data for genomic DNA-derived signals with ValidPrime
  • Correction of RT-qPCR data for genomic DNA-derived signals with ValidPrime (en)
skos:notation
  • RIV/86652036:_____/12:00379016!RIV13-AV0-86652036
http://linked.open...avai/riv/aktivita
http://linked.open...avai/riv/aktivity
  • Z(AV0Z50520701)
http://linked.open...iv/cisloPeriodika
  • 7
http://linked.open...vai/riv/dodaniDat
http://linked.open...aciTvurceVysledku
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  • 128845
http://linked.open...ai/riv/idVysledku
  • RIV/86652036:_____/12:00379016
http://linked.open...riv/jazykVysledku
http://linked.open.../riv/klicovaSlova
  • TIME QUANTITATIVE PCR; POLYMERASE-CHAIN-REACTION; GENE-EXPRESSION (en)
http://linked.open.../riv/klicoveSlovo
http://linked.open...odStatuVydavatele
  • GB - Spojené království Velké Británie a Severního Irska
http://linked.open...ontrolniKodProRIV
  • [64B75F43CB12]
http://linked.open...i/riv/nazevZdroje
  • Nucleic Acids Research
http://linked.open...in/vavai/riv/obor
http://linked.open...ichTvurcuVysledku
http://linked.open...cetTvurcuVysledku
http://linked.open...UplatneniVysledku
http://linked.open...v/svazekPeriodika
  • 40
http://linked.open...iv/tvurceVysledku
  • Kubista, Mikael
  • Švec, David
  • Abot, A.
  • Arnal, J.-F.
  • Iacovoni, J. S.
  • Laurell, H.
  • Maoret, J.-J.
http://linked.open...ain/vavai/riv/wos
  • 000303164400005
http://linked.open...n/vavai/riv/zamer
issn
  • 0305-1048
number of pages
http://bibframe.org/vocab/doi
  • 10.1093/nar/gkr1259
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