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A novel aldo-keto reductase gene is involved in 6'-deoxychalcone biosynthesis in dahlia (Dahlia variabilis).
Ohno, Sho; Yamada, Haruka; Maruyama, Kei; Deguchi, Ayumi; Kato, Yasunari; Yokota, Mizuki; Tatsuzawa, Fumi; Hosokawa, Munetaka; Doi, Motoaki.
Affiliation
  • Ohno S; Graduate School of Agriculture, Kyoto University, Kyoto, Kyoto, 606-8502, Japan. ohno.sho.3c@kyoto-u.ac.jp.
  • Yamada H; Graduate School of Agriculture, Kyoto University, Kyoto, Kyoto, 606-8502, Japan.
  • Maruyama K; Graduate School of Agriculture, Kyoto University, Kyoto, Kyoto, 606-8502, Japan.
  • Deguchi A; Graduate School of Agriculture, Kyoto University, Kyoto, Kyoto, 606-8502, Japan.
  • Kato Y; Chiba University, Chiba, 271-8510, Japan.
  • Yokota M; Graduate School of Agriculture, Kyoto University, Kyoto, Kyoto, 606-8502, Japan.
  • Tatsuzawa F; Graduate School of Agriculture, Kyoto University, Kyoto, Kyoto, 606-8502, Japan.
  • Hosokawa M; Faculty of Agriculture, Iwate University, Iwate, Morioka, 020-8550, Japan.
  • Doi M; Graduate School of Agriculture, Kyoto University, Kyoto, Kyoto, 606-8502, Japan.
Planta ; 256(3): 47, 2022 Jul 24.
Article in En | MEDLINE | ID: mdl-35871668
ABSTRACT
MAIN

CONCLUSION:

A novel gene belonging to the aldo-keto reductase 13 family is involved in isoliquiritigenin biosynthesis in dahlia. The yellow pigments of dahlia flowers are derived from 6'-deoxychalcones, which are synthesized via a two-step process, involving the conversion of 3-malonyl-CoA and 4-coumaloyl-CoA into isoliquiritigenin in the first step, and the subsequent generation of butein from isoliquiritigenin. The first step reaction is catalyzed by chalcone synthase (CHS) and aldo-keto reductase (AKR). AKR has been implicated in the isoflavone biosynthesis in legumes, however, isolation of butein biosynthesis related AKR members are yet to be reported. A comparative RNA-seq analysis between two dahlia cultivars, 'Shukuhai' and its butein-deficient lateral mutant 'Rinka', was used in this study to identify a novel AKR gene involved in 6'-deoxychalcone biosynthesis. DvAKR1 encoded a AKR 13 sub-family protein with significant differential expression levels, and was phylogenetically distinct from the chalcone reductases, which belongs to the AKR 4A sub-family in legumes. DNA sequence variation and expression profiles of DvAKR1 gene were correlated with 6'-deoxychalcone accumulation in the tested dahlia cultivars. A single over-expression analysis of DvAKR1 was not sufficient to initiate the accumulation of isoliquiritigenin in tobacco, in contrast, its co-overexpression with a chalcone 4'-O-glucosyltransferase (Am4'CGT) from Antirrhinum majus and a MYB transcription factor, CaMYBA from Capsicum annuum successfully induced isoliquiritigenin accumulation. In addition, DvAKR1 homologous gene expression was detected in Coreopsideae species accumulating 6'-deoxychalcone, but not in Asteraceae species lacking 6'-deoxychalcone production. These results not only demonstrate the involvement of DvAKR1 in the biosynthesis of 6'-deoxychalcone in dahlia, but also show that 6'-deoxychalcone occurrence in Coreopsideae species developed evolutionarily independent from legume species.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Dahlia / Chalcones Type of study: Prognostic_studies Language: En Journal: Planta Year: 2022 Type: Article Affiliation country: Japan

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Dahlia / Chalcones Type of study: Prognostic_studies Language: En Journal: Planta Year: 2022 Type: Article Affiliation country: Japan