Abstract
The variability of transcript accumulation of six genes encoding Chloropyll-a/b (Chla/b) binding protein, Nicotinamide Adenine Dinucleotide Hydride (NADH) dehydrogenase, Histone H3 (H3), DEAD-box RNA helicase 1 (DRH1) and Glyceraldehyde-3-phosphate dehydrogenase (GAPDH) and of the 7SL component of the signal recognition particle (7SL-RNA), was estimated in leaves and female inflorescences of the two hop cultivars, White Golding and Admiral at different developmental stages by RT-PCR. The value of these genes as internal, normalization controls in gene transcript accumulation studies was assessed. The combination of the three housekeeping genes DRH1, GAPDH and 7SL-RNA as internal standards for hop, provided reliable results in the quantitative analysis of the transcript accumulation of Hua Enhancer 1 transcription factor (HEN1) homologue in hop tissues and is recommended for future studies of gene expression in female hop tissues.
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Abbreviations
- Chla/b:
-
Chloropy1l-a/b
- NADH:
-
Nicotinamide Adenine Dinucleotide Hydride
- DRH1:
-
DEAD-box RNA Helicase 1
- GAPDH:
-
Glyceraldehyde-3-Phosphate Dehydrogenase
- H3:
-
Histone 3
- 7SL-RNA:
-
7SL component of the signal recognition particle
- HEN1:
-
Hua Enhancer 1
- Ct-value:
-
the point at which the measured fluorescence of PCR products crosses a threshold value
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Maloukh, L., Matousek, J., Van Bockstaele, E. et al. Housekeeping Gene Selection for Real Time-PCR Normalization in Female Hop (Humulus lupulus L) Tissues. J. Plant Biochem. Biotechnol. 18, 53–58 (2009). https://doi.org/10.1007/BF03263295
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DOI: https://doi.org/10.1007/BF03263295