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Tatsuzawa, F.

Publications and source records attributed to Tatsuzawa, F..

2 recordsLinked to original sources

Unstable anthocyanin pigmentation in Streptocarpus sect. Saintpaulia (African violet) is due to variant selectivity of a single MYB gene

O_LISaintpaulia (African violet) pigmentation is notoriously unstable, particularly following passage through tissue culture, but the instability mechanism is unknown. White-striped petals were thought to be due to epigenetics, but the genes involved are unknown. We confirmed that white stripes result from epigenetic regulation based on the flower color traits of plants obtained from tissue culture. C_LIO_LIGene expression in several plant lines, anthocyanin quantification, bisulfite sequencing, and methylation analyses were used to demonstrate the presence of a single MYB gene responsible for pigment variation. We identified SiMYB2 as the cause of variations in tissue color patterning, and that two RNAs were generated from SiMYB2. SiMYB2-Long was expressed in colored tissues, while SiMYB2-Short was expressed only in non-colored tissues. Functional analyses revealed that SiMYB2-Long is an anthocyanin biosynthesis activator and SiMYB2-Short is non-functional. Exon 3 of SiMYB2 was generated by the insertion of a transposon-like sequence. A mutant lacking the element was obtained from cultivars with non-colored tissues. Anthocyanin content and SiMYB2-Long expression in the mutant were greatly increased compared to wild type. C_LIO_LIOur results suggest that the white-striped petals of Saintpaulia are not formed by periclinal chimeras but thorough the transcriptional selectivity of epigenetically regulated SiMYB2. C_LI

plant biology↗

Identification of a novel chalcone reductase gene for isoliquiritigenin biosynthesis in dahlia (Dahlia variabilis)

Butein is one of flavonoids conferring bright yellow flower color and is a precursor of aurone in some species. Butein is synthesized by two steps, 3-malonyl CoA and 4-coumaloyl CoA are converted to isoliquiritigenin in the first step, and then isoliquiritigenin is converted to butein in the second step. In the first step, chalcone synthase (CHS) and chalcone reductase (CHR) catalyze this reaction, however, CHR has been reported for the isoflavone biosynthesis pathway in legumes, and CHR for butein biosynthesis has not yet been isolated. In this study, we report CHR that is evolutionally different gene from legume species is involved in isoliquiritigenin biosynthesis in dahlia. To isolate CHR gene, we conducted comparative RNA-seq analysis between Shukuhai and its butein-loss lateral mutant Rinka. We found DvCHR showed significant difference in expression levels that encodes an aldo-keto reductase (AKR) 13 family protein, which was phylogenetically different from legume CHRs belonging to AKR4A family. Gene expression levels and genotype of DvCHR were correlated with butein accumulation among various dahlia cultivars. Though single over expression of DvCHR was not able to accumulate isoliquiritigenin in tobacco, co-overexpression of DvCHR with a chalcone glucosyltransferase Am4'CGT and a MYB transcription factor CaMYBA successfully induced isoliquiritigenin accumulation. In addition, DvCHR homologous gene expression was detected from butein or aurone accumulating Coreopsideae species but not from non-butein or non-aurone accumulating Asteraceae species. These results indicated DvCHR functions as chalcone reductase for butein biosynthesis in dahlia, and isoliquiritigenin biosynthesis in Coreopsideae species has been developed independently from legume species.

plant biology↗