文献类型： 外文期刊

作者： Li, Li ¹ ; Li, Xiao'an ¹ ; Gao, Xiaoli ³ ; Liao, Wenhua ³ ; Guo, Huihui ¹ ; He, Cailin ¹ ; Lu, Jing ¹ ; Ye, Xueling ¹ ; Sun, Wenjun ¹ ; Liu, Changying ¹ ; Fan, Yu ¹ ; Bai, Xue ¹ ; Wu, Qi ¹ ;

作者机构： 1.Chengdu Univ, Sichuan Engn & Technol Res Ctr Coarse Cereal Indus, Key Lab Coarse Cereal Proc,Coll Food & Biol Engn, Sch Food & Biol Engn,Minist Agr & Rural Affairs, Chengdu 610106, Sichuan, Peoples R China

2.Sichuan Agr Univ, State Key Lab Crop Gene Explorat & Utilizat Southw, Chengdu 611130, Sichuan, Peoples R China

3.Tibet Acad Agr & Anim Husb Sci, Res Inst Agr Sci, Lhasa 850032, Xizang, Peoples R China

关键词： Betalain biosynthesis; CqCYP76AD; CqDODA; Evolutionary history; CqCYP76AD-CqDODA operon; Hairy root transformation; Quinoa

期刊名称：PLANT PHYSIOLOGY AND BIOCHEMISTRY （ 影响因子：5.7； 五年影响因子：6.4 ）

ISSN： 0981-9428

年卷期： 2025 年 220 卷

页码：

收录情况： SCI

摘要： Betalains are water-soluble pigments mainly distributed in the core Caryophyllales plants. Betalains provide plant with striking colors to attract pollinators and are beneficial to human health due to the strong antioxidant activity. To date, many studies regarding to betalain biosynthesis have been exerted in sugar beet (Beta vulgaris) and four-O-clock (Mirabilis jalapa), however, the key regulators in betalain pigmentation of quinoa (Chenopodium quinoa) remain to be elucidated. CYP76AD and DODA genes encode core enzymes converting L-DOPA to cycloDOPA and betalamic acid, respectively, in betalain biosynthesis. In this study, 44 CqCYP76AD (5 alpha-clade, 6 beta-clade and 33 gamma-clade homologs) and 18 CqDODA (10 alpha-clade, 2 beta-clade and 6 gamma-clade homologs) members were identified in quinoa genome. Expression analysis and cis-element analysis indicated that light and ABA are involved in the regulation of CqCYP76AD and CqDODA. We found application of exogenous ABA and darkness repressed the betalain production in quinoa seedlings. Tandem duplication is the major driving force for CqCYP76AD and CqDODA family expansion. Evolutionary history analysis on the duplication events of quinoa and its close relatives, sugar beet, C. pallidicaule, C. suecicum and C. formosanum, identified the quinoa-specific tandem duplications CqCYP76AD-alpha 2/-alpha 3, CqDODA-alpha 1/-alpha 6 in Chr04, and CqCYP76AD-alpha 1/-alpha 4/-alpha 5, CqDODA- alpha 3/-alpha 4/-alpha 5 in Chr03, which are absent in sugar beet. The close co-location of the CqCYP76AD-alpha-CqDODA-alpha gene clusters suggests they are putative enhanced regulatory units for betalain biosynthesis in quinoa, similar to the operon BvCYP76AD1-BvDODA1 in sugar beet. The functions of alpha-, beta- and gamma-clade CqCYP76ADs and CqDODAs were investigated by transient expression system in tobacco leaves and hairy root transformation in quinoa. The results indicated that CqCYP76AD-alpha 1, CqCYP76AD-beta 3, CqDODA-alpha 1, CqDODA-alpha 3 and CqDODA-alpha 5 are the important positive regulators for betalain accumulation in quinoa. Correlation between pigment contents and expression levels at different developmental stages indicates their roles in pigmentation of leaf, stem and spike tissues of in betalain-enriched quinoa. Overall, this study performed genome-wide identification and functional characterization of the important functional enzymes of CqCYP76ADs and CqDODAs for betalain biosynthesis in quinoa, which will deep our understanding of the mechanisms of betalain pigmentation in quinoa.