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Evaluation of reference genes for reverse transcription quantitative real-time PCR (RT-qPCR) studies in Silene vulgaris considering the method of cDNA preparation
- 1.0477711 - UEB-Q 2018 RIV US eng J - Journal Article
Koloušková, Pavla - Stone, James D. - Štorchová, Helena
Evaluation of reference genes for reverse transcription quantitative real-time PCR (RT-qPCR) studies in Silene vulgaris considering the method of cDNA preparation.
PLoS ONE. Roč. 12, č. 8 (2017), č. článku e0183470. E-ISSN 1932-6203
R&D Projects: GA MŠk(CZ) LH15075; GA ČR(CZ) GA16-09220S
Institutional support: RVO:61389030
Keywords : CYTOPLASMIC MALE-STERILITY * SUITABLE REFERENCE GENES * INTERNAL CONTROL GENES
Subject RIV: EB - Genetics ; Molecular Biology
OBOR OECD: Plant sciences, botany
Impact factor: 2.766, year: 2017
Accurate gene expression measurements are essential in studies of both crop and wild plants. Reverse transcription quantitative real-time PCR (RT-qPCR) has become a preferred tool for gene expression estimation. A selection of suitable reference genes for the normalization of transcript levels is an essential prerequisite of accurate RT-qPCR results. We evaluated the expression stability of eight candidate reference genes across roots, leaves, flower buds and pollen of Silene vulgaris (bladder campion), a model plant for the study of gynodioecy. As random priming of cDNA is recommended for the study of organellar transcripts and poly(A) selection is indicated for nuclear transcripts, we estimated gene expression with both random-primed and oligo(dT)-primed cDNA. Accordingly, we determined reference genes that perform well with oligo(dT)- and random-primed cDNA, making it possible to estimate levels of nucleus-derived transcripts in the same cDNA samples as used for organellar transcripts, a key benefit in studies of cyto-nuclear interactions. Gene expression variance was estimated by RefFinder, which integrates four different analytical tools. The SvACT and SvGAPDH genes were the most stable candidates across various organs of S. vulgaris, regardless of whether pollen was included or not.
Permanent Link: http://hdl.handle.net/11104/0273966
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