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Identification of Reference Genes for Real- Time Quantitative PCR Experiments in the Liverwort Marchantia polymorpha.

Saint-Marcoux, D., et al. · 2015 · PLoS ONE   research

doi:10.1371/journal.pone.0118678   PMID:25798897   PMC4370483

Linked genes (13)  0 core 13 peripheral

Gene ID Name Evidence / Role Function (this paper)
MpACT missing experimental tool Candidate reference gene with one of the lowest z-scores; recommended together with MpAPT as a stable normalizer.
Mp3g25140 MpAPT experimental tool Candidate reference gene with one of the lowest z-scores; most suitable and recommended for generic qPCR normalization.
MpCUL missing experimental tool Candidate reference gene showing moderate expression stability across the conditions tested.
Mp3g23400 MpEF1 experimental tool Candidate reference gene; expression-stable and suitable for normalization in developmental comparisons.
MpELF5 missing experimental tool Candidate reference gene showing moderate expression stability across the conditions tested.
MpGAPC1 missing experimental tool Candidate reference gene with high transcript variability across groups; unsuitable as a reference gene.
MpH3 missing experimental tool Candidate reference gene with low variation under hormone treatment but high variation in other contexts.
MpNRT2 missing experimental tool Nitrate transporter used as a target to demonstrate normalization accuracy; induced ~14-27 fold under nitrate starvation.
MpPEX missing experimental tool Candidate reference gene showing moderate expression stability across the conditions tested.
MpPHT1 missing experimental tool Phosphate transporter used as a target to validate normalization; induced ~4-5 fold under phosphate starvation.
Mp4g07110 MpSAND missing experimental tool Candidate reference gene suitable for development and abiotic stress but elevated after hormone treatments.
MpTUB8 missing experimental tool Candidate reference gene showing large expression variation; unsuitable for qPCR normalization.
MpUBQ10 missing experimental tool Candidate reference gene whose transcript levels varied most; judged unsuitable for qPCR normalization.