文献类型： 外文期刊

作者： Liu, Huabo ¹ ; Wei, Lingzhi ¹ ; Ni, Yang ¹ ; Chang, Linlin ¹ ; Dong, Jing ¹ ; Zhong, Chuanfei ¹ ; Sun, Rui ¹ ; Li, Shuangtao ¹ ; Xiong, Rong ¹ ; Wang, Guixia ¹ ; Sun, Jian ¹ ; Zhang, Yuntao ¹ ; Gao, Yongshun ¹ ;

作者机构： 1.Beijing Acad Forestry & Pomol Sci, Inst Forestry & Pomol, Beijing, Peoples R China

2.Minist Agr & Rural Affairs, Key Lab Biol & Genet Improvement Hort Crops North, Beijing, Peoples R China

3.Beijing Engn Res Ctr Strawberry, Beijing, Peoples R China

4.Minist Agr & Rural Affairs, Inspection & Testing Lab Fruits & Nursery Stocks B, Beijing, Peoples R China

关键词： Fragaria x ananassa; ascorbic acid biosynthesis; genome-wide analysis; AKR; expression pattern

期刊名称：FRONTIERS IN PLANT SCIENCE （ 影响因子：6.627； 五年影响因子：7.255 ）

ISSN： 1664-462X

年卷期： 2022 年 13 卷

页码：

收录情况： SCI

摘要： Ascorbic acid (AsA) is an important antioxidant for scavenging reactive oxygen species and it is essential for human health. Strawberry (Fragaria x ananassa) fruits are rich in AsA. In recent years, strawberry has been regarded as a model for non-climacteric fruit ripening. However, in contrast to climacteric fruits, such as tomato, the regulatory mechanism of AsA accumulation in strawberry fruits remains largely unknown. In this study, we first identified 125 AsA metabolism-related genes from the cultivated strawberry "Camarosa" genome. The expression pattern analysis using an available RNA-seq data showed that the AsA biosynthetic-related genes in the D-mannose/L-galactose pathway were downregulated remarkably during fruit ripening which was opposite to the increasing AsA content in fruits. The D-galacturonate reductase gene (GalUR) in the D-Galacturonic acid pathway was extremely upregulated in strawberry receptacles during fruit ripening. The FaGalUR gene above belongs to the aldo-keto reductases (AKR) superfamily and has been proposed to participate in AsA biosynthesis in strawberry fruits. To explore whether there are other genes in the AKR superfamily involved in regulating AsA accumulation during strawberry fruit ripening, we further implemented a genome-wide analysis of the AKR superfamily using the octoploid strawberry genome. A total of 80 FaAKR genes were identified from the genome and divided into 20 subgroups based on phylogenetic analysis. These FaAKR genes were unevenly distributed on 23 chromosomes. Among them, nine genes showed increased expression in receptacles as the fruit ripened, and notably, FaAKR23 was the most dramatically upregulated FaAKR gene in receptacles. Compared with fruits at green stage, its expression level increased by 142-fold at red stage. The qRT-PCR results supported that the expression of FaAKR23 was increased significantly during fruit ripening. In particular, the FaAKR23 was the only FaAKR gene that was significantly upregulated by abscisic acid (ABA) and suppressed by nordihydroguaiaretic acid (NDGA, an ABA biosynthesis blocker), indicating FaAKR23 might play important roles in ABA-mediated strawberry fruit ripening. In a word, our study provides useful information on the AsA metabolism during strawberry fruit ripening and will help understand the mechanism of AsA accumulation in strawberry fruits.