Selection and validation of reference genes for quantitative gene expression analyses in persimmon (Diospyros kaki Thunb.) using real-time quantitative PCR
Background and aims Persimmon ( Diospyros kaki ) is an economically important fruit tree species with complex flowering characteristics. To obtain accurate expression pattern analysis results, it is vital to select a reliable gene for the normalization of real-time quantitative polymerase chain reac...
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Veröffentlicht in: | Biologia futura 2019-12, Vol.70 (4), p.261-267 |
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Hauptverfasser: | , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Background and aims
Persimmon (
Diospyros kaki
) is an economically important fruit tree species with complex flowering characteristics. To obtain accurate expression pattern analysis results, it is vital to select a reliable gene for the normalization of real-time quantitative polymerase chain reaction data. The aim of this study was to identify the optimal internal control gene among six candidate genes for gene expression analysis in different persimmon organs and developmental stages.
Materials and methods
This analysis was conducted using geNorm and NormFinder software to show differences in the stability of the six reference genes among tissues and floral developmental stages of the same plant.
Results
Although genes that exhibited moderate expression in NormFinder revealed slightly different expression stabilities than those obtained by geNorm, both sets of results showed that
GAPDH was
the best reference gene in different organs and floral buds at different developmental stages, whereas
18SrRNA
was the least stable gene.
Conclusions
Based on the overall ranking,
GAPDH
is the most suitable reference gene and is highly recommended for gene expression studies in different organs and different developmental stages of persimmon. This study provides useful reference data for future gene expression studies and will contribute to improving the accuracy of gene expression results in persimmon. |
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ISSN: | 2676-8615 2676-8607 |
DOI: | 10.1556/019.70.2019.24 |