小麦GPX基因鉴定、表达与自然等位变异分析OA
Identification,Expression and Natural Allelic Variation Analysis of Wheat GPX Genes
提高谷胱甘肽过氧化物酶(GPX)活性是培育富硒小麦(Triticum aestivum L.)的潜在途径.为了鉴定小麦GPX基因家族成员,明确成员在不同组织及不同硒(Se)处理下的表达水平,本研究利用生物信息学与分子生物学方法鉴定和分析小麦GPX基因家族成员、特性及功能,并研究了 TaGPX基因的结构、理化性质和功能表达.在普通小麦中检出14个GPX基因,不均匀分布在2、4、6、7号染色体A、B、D同源群上;比对结果显示,TaGPX基因的亚细胞定位大部分位于叶绿体和线粒体上,外显子数为5~6个,基序数目较为相似.启动子区顺式作用元件预测结果显示,TaGPX基因家族中多个基因富含响应非生物胁迫的功能元件.通过构建GPX进化树,发现小麦与节节麦的GPX基因亲缘关系最近,基因分化相似性较高.转录组数据显示TaGPX基因家族的多数基因在小麦叶片中表达量高,旗叶期和蜡熟期时表达量最高,推测此基因家族参与叶绿体内活性氧(ROS)清除相关的生理过程.TaGPX基因在叶片中的表达量明显高于种子部位,结合小麦DNA变异分析和转录组数据推测TaGPX的单核苷酸多态性(SNP)位点变异是提高小麦自身系统ROS处理能力的原因之一.对小麦不同组织的GPX基因表达量测定及硒盐处理下GPX表达进行差异分析,结果表明:TaGPX3.2A在小麦不同组织中相对表达量最高,推测在硒处理下硫会与硒竞争吸收位点,抑制硒的吸收,去硫施硒能提高TaGPX基因的表达水平.本研究为利用TaGPX基因提高小麦硒富集水平奠定了基础.
Enhancing glutathione peroxidase(GPX)activity is a promising strategy for developing selenium-enriched wheat(Triticum aestivum L.).To identify members of the wheat GPX gene family and characterize their expression patterns across tissues,developmental stages,and selenium(Se)treatments,this study integrated bioinformatics and molecular biology approaches to systematically characterize e the structure,physicochemical properties,and functional expression of TaGPX genes.Fourteen GPX genes were detected in common wheat,unevenly distributed across chromosomes 2,4,6,and 7 of the A,B,and D homologous groups.Comparative analysis showed that TaGPX genes located on homologous chromosomes were predominantly localized to chloroplasts and chromosomes,with 5 to 6 exons and similar motif numbers.Promoter cis-acting element prediction indicated that most aGPX genes harbor abundant regulatory elements responsive to abiotic stress.By constructing a GPX evolutionary tree,it was found that wheat GPX genes are most closely related to those of Aegilops tauschii,with high similarity in gene differentiation.Transcriptome data showed that most TaGPX genes are highly expressed in leaves,with the highest expression levels at the flag leaf and wax ripening stage,suggesting the involvement of this gene family in scavenging reactive oxygen species(ROS)clearance within chloroplasts.The expression level of TaGPX genes in leaves was significantly higher than in seeds.Integrative analysis of genomic variation and transcriptome profiles implied that the SNP variations in TaGPX genes may contribute to improved ROS detoxification capacity in wheat system itself.Quantitative expression analysis across tissues and selenium salt treatment showed that TaGPX3.2A had the highest relative expression level.It was speculated that sulfur would compete with selenium for absorption sites under selenium supplementation,thereby limiting selenium absorption.De-sulfurization combined with selenium application could increase the expression level of TaGPX genes.This study laid a foundation for leveraging TaGPX genes to improve selenium biofortification in wheat.
王新宇;王伟;郭子浩;史小霞;郝昱宁;韦小龙;吕晋慧;张春来
山西农业大学农学院,山西太谷 030801山西农业大学农学院,山西太谷 030801山西农业大学农学院,山西太谷 030801山西农业大学农学院,山西太谷 030801山西农业大学农学院,山西太谷 030801山西农业大学农学院,山西太谷 030801山西农业大学林学院,山西太谷 030801山西农业大学农学院,山西太谷 030801
普通小麦(Triticum aestivum L.)谷胱甘肽过氧化物酶生物信息分析非生物胁迫
common wheat(Triticum aestivum L.)glutathione peroxidasebioinformatics analysisabiotic stress
《核农学报》 2026 (7)
1321-1330,10
国家自然科学基金项目(31971944),山西省教育厅研究生教育创新计划实践创新项目(2023SJ109),山西省教育厅专业建设项目(J20220211),山西农谷建设科研专项(SXNGJSKYZX201702)
评论