Liu Huabo, Wei Lingzhi, Ni Yang, Chang Linlin, Dong Jing, Zhong Chuanfei, Sun Rui, Li Shuangtao, Xiong Rong, Wang Guixia, Sun Jian, Zhang Yuntao, Gao Yongshun
Institute of Forestry and Pomology, Beijing Academy of Forestry and Pomology Sciences, Beijing, China.
Key Laboratory of Biology and Genetic Improvement of Horticultural Crops (North China), Ministry of Agriculture and Rural Affairs, Beijing, China.
Front Plant Sci. 2022 Jul 6;13:954505. doi: 10.3389/fpls.2022.954505. eCollection 2022.
Ascorbic acid (AsA) is an important antioxidant for scavenging reactive oxygen species and it is essential for human health. Strawberry ( × ) 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 () in the D-Galacturonic acid pathway was extremely upregulated in strawberry receptacles during fruit ripening. The 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 genes were identified from the genome and divided into 20 subgroups based on phylogenetic analysis. These genes were unevenly distributed on 23 chromosomes. Among them, nine genes showed increased expression in receptacles as the fruit ripened, and notably, was the most dramatically upregulated 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 was increased significantly during fruit ripening. In particular, the was the only gene that was significantly upregulated by abscisic acid (ABA) and suppressed by nordihydroguaiaretic acid (NDGA, an ABA biosynthesis blocker), indicating 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.
抗坏血酸(AsA)是清除活性氧的重要抗氧化剂,对人体健康至关重要。草莓(×)果实富含AsA。近年来,草莓被视为非跃变型果实成熟的模型。然而,与跃变型果实如番茄不同,草莓果实中AsA积累的调控机制在很大程度上仍不清楚。在本研究中,我们首先从栽培草莓“卡玛罗莎”基因组中鉴定出125个与AsA代谢相关的基因。利用现有的RNA-seq数据进行的表达模式分析表明,D-甘露糖/L-半乳糖途径中与AsA生物合成相关的基因在果实成熟过程中显著下调,这与果实中AsA含量的增加相反。D-半乳糖醛酸途径中的D-半乳糖醛酸还原酶基因()在草莓果实成熟过程中在花托中极度上调。上述基因属于醛酮还原酶(AKR)超家族,已被认为参与草莓果实中AsA的生物合成。为了探索AKR超家族中是否有其他基因参与调控草莓果实成熟过程中AsA的积累,我们利用八倍体草莓基因组对AKR超家族进行了全基因组分析。从基因组中总共鉴定出80个基因,并根据系统发育分析将其分为20个亚组。这些基因不均匀地分布在23条染色体上。其中,9个基因在果实成熟时在花托中的表达增加,值得注意的是,是花托中上调最显著的基因。与绿果期果实相比,其在红果期的表达水平增加了142倍。qRT-PCR结果支持在果实成熟过程中表达显著增加。特别是,是唯一受脱落酸(ABA)显著上调并被去甲二氢愈创木酸(NDGA,一种ABA生物合成阻滞剂)抑制的基因,表明可能在ABA介导的草莓果实成熟中起重要作用。总之,我们的研究为草莓果实成熟过程中的AsA代谢提供了有用信息,并将有助于理解草莓果实中AsA积累的机制。