Aziz Shahid, Germano Thais Andrade, Sousa Do Nascimento Maria Adriele Dos Santos de, Dos Santos Clesivan Pereira, Arnholdt-Schmitt Birgit, de Miranda Maria Raquel Alcântara, Gomes Mara Menezes de Assis, Mazorra Morales Luis Miguel, Ayub Ricardo Antônio, Oliveira Jurandi Gonçalves de, Costa José Hélio
Department of Biochemistry, Institute of Chemistry, University of São Paulo, São Paulo 05508-000, SP, Brazil.
Functional Genomics and Bioinformatics, Department of Biochemistry and Molecular Biology, Federal University of Ceara, Fortaleza 60451-970, CE, Brazil.
Int J Mol Sci. 2025 May 14;26(10):4678. doi: 10.3390/ijms26104678.
Ascorbic acid (AsA) is an essential plant metabolite that acts primarily as an antioxidant, regulates cell division and elongation, and enhances stress tolerance. Despite its crucial physiological role, the biosynthesis of AsA in , a major crop of significant commercial importance, remains largely unexplored. This gap highlights the need for a thorough investigation of AsA biosynthesis pathways and their role in optimizing the nutritional value and stress tolerance of soybeans. This study identified 41 key genes linked to four AsA biosynthesis pathways in , highlighting specific gene duplications compared to . Their expression levels were assessed by analyzing a diverse set of RNA-Seq data from the NCBI database. Additionally, to cross-validate the expression levels of genes and the accumulation levels of AsA in the principal tissues, plants were grown under controlled conditions following the protocols from selected RNA-seq experiments. Genes associated with the D-mannose/L-galactose pathway exhibited ubiquitous expression, and the expression patterns of genes from alternative pathways reflected their responsiveness to specific tissues or environmental conditions. Germination and leaf development were accompanied by strong expression of gene members from all pathways, whereas leaf aging was characterized by downregulation. Specific gene members, such as (D-mannose/L-galactose pathway), (L-gulose pathway), and (Myo-inositol pathway) were highly stress-responsive and linked to stress-resistant genotypes and cultivars. Consistent with gene expression analyses, the quantification of AsA revealed the highest mass fractions in young leaves and germinating seeds. However, AsA mass fractions were significantly reduced or unchanged under stress conditions, depending on the type of stress and the duration of exposure. Overall, this study validated the relevance of AsA biosynthesis pathways in soybeans, highlighting key genes that could be targeted to enhance stress tolerance and improve ascorbate production, thereby boosting the nutritional value of soybeans.
抗坏血酸(AsA)是一种必需的植物代谢产物,主要作为抗氧化剂发挥作用,调节细胞分裂和伸长,并增强胁迫耐受性。尽管其具有关键的生理作用,但在具有重要商业价值的主要作物大豆中,AsA的生物合成在很大程度上仍未得到充分研究。这一差距凸显了全面研究AsA生物合成途径及其在优化大豆营养价值和胁迫耐受性方面作用的必要性。本研究确定了与大豆中四条AsA生物合成途径相关的41个关键基因,突出了与其他物种相比特定的基因重复情况。通过分析来自NCBI数据库的各种RNA测序数据评估了它们的表达水平。此外,为了交叉验证主要组织中基因的表达水平和AsA的积累水平,按照选定RNA测序实验的方案在可控条件下种植大豆植株。与D-甘露糖/L-半乳糖途径相关的基因表现出普遍表达,其他途径基因的表达模式反映了它们对特定组织或环境条件的响应。发芽和叶片发育伴随着所有途径基因成员的强烈表达,而叶片衰老的特征是基因下调。特定的基因成员,如GME(D-甘露糖/L-半乳糖途径)、GULS1(L-古洛糖途径)和MIOX(肌醇途径)对胁迫高度响应,并与抗逆基因型和品种相关。与基因表达分析一致,AsA的定量分析显示幼叶和发芽种子中的质量分数最高。然而,根据胁迫类型和暴露持续时间,胁迫条件下AsA的质量分数显著降低或不变。总体而言,本研究验证了AsA生物合成途径在大豆中的相关性,突出了可作为靶点以增强胁迫耐受性和提高抗坏血酸产量从而提升大豆营养价值的关键基因。