薰衣草LabHLH35基因的克隆及表达分析OA
Cloning and Expression Analysis of LabHLH35 Gene in Lavender(Lavandula angustifolia)
薰衣草(Lavandula angustifolia)因独特的花色及芳香特性而具有较高的观赏价值.花色是薰衣草观赏价值的重要评价指标之一,花青素是影响其花瓣呈色的核心物质,而 bHLH 转录因子在调控植物花青素生物合成途径中发挥重要作用.为探究薰衣草花青素生物合成调控机制并为培育新品种提供候选基因,本研究从薰衣草花器官中克隆出 LabHLH35 基因,并对其进行生物信息学分析、组织特异性表达分析和酵母自激活验证分析.结果表明,LabHLH35 基因全长 678 bp,编码 225 个氨基酸.LabHLH35 蛋白属于不稳定的亲水蛋白,含有碱性螺旋-环-螺旋(Helix-Loop-Helix,HLH)保守结构域,与鼠尾草(Salvia divinorum)的SdbHLH35蛋白和一串红(Salvia splendens)的 SsbHLH35 蛋白亲缘关系较近;定位于细胞核内,具有转录自激活活性.LabHLH35 在薰衣草不同组织中和不同花发育时期均有表达,但在花中的表达量最高,表现出明显的组织表达特异性,这与花中花青素含量较高具有一致性.本研究结果初步分析了 LabHLH35 基因的功能,为进一步探究转录因子 LabHLH35 在薰衣草花青素合成中的调控作用奠定了基础.
Lavender(Lavandula angustifolia)possesses significant ornamental value due to its unique floral coloration and aromatic properties.Flower color is a key determinant of its ornamental value,and antho-cyanin is the core matter influencing flower color.The bHLH transcription factors play crucial roles in regula-ting anthocyanin biosynthesis pathways in plants.To elucidate the regulatory mechanisms of anthocyanin bio-synthesis in lavender and identify candidate genes for novel cultivar breeding,the LabHLH35 gene was cloned from lavender floral organs and the bioinformatics analysis,tissue-specific expression profiling,and yeast self-activation assays were conducted in this study.The length of LabHLH35 gene was 678 bp,encoding a 225-a-mino acid protein classified as an unstable hydrophilic protein.The LabHLH35 protein contained a conserved basic Helix-Loop-Helix(bHLH)domain,showing close phylogenetic relationships with SdbHLH35(Salvia divinorum)and SsbHLH35(Salvia splendens)proteins.Subcellular localization confirmed its nuclear localiza-tion,and yeast assays demonstrated its transcriptional self-activation activity.Expression analysis revealed that LabHLH35 was expressed across various tissues and floral developmental stages,with the highest expression level observed in flowers,consistent with more anthocyanin accumulation in flowers,indicating a distinct tis-sue-specific expression pattern.This study provided preliminary insights into the functional characteristics of the LabHLH35 gene and could lay the foundation for further investigation on the regulatory role of the LabHLH35 transcription factor in lavender anthocyanin synthesis.
黄佳慧;王爱凡;苏秀娟
新疆农业大学农学院,新疆 乌鲁木齐 830052||新疆农业大学薰衣草研究所/新疆作物生物育种重点实验室,新疆 乌鲁木齐 830052新疆农业大学农学院,新疆 乌鲁木齐 830052||新疆农业大学薰衣草研究所/新疆作物生物育种重点实验室,新疆 乌鲁木齐 830052新疆农业大学农学院,新疆 乌鲁木齐 830052||新疆农业大学薰衣草研究所/新疆作物生物育种重点实验室,新疆 乌鲁木齐 830052
农业科技
薰衣草LabHLH35转录因子基因克隆表达分析转录激活
LavenderLabHLH35 transcription factorGene cloningExpression analysisTranscrip-tional activation
《山东农业科学》 2026 (7)
31-39,9
新疆维吾尔自治区"天山英才"青年拔尖人才项目(2023TSYCCX0017)
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