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丹参转录因子基因SmbHLH59的克隆与表达特征分析OA

Cloning and Expression Features of Transcription Factor Gene SmbHLH59 from Salvia miltiorrhiza

中文摘要英文摘要

丹参酮是丹参的主要药效成分,合成途径受多种因子的调控.碱性螺旋-环-螺旋(basic helix-loop-helix,bHLH)转录因子家族对植物的生长代谢、活性物质合成、胁迫响应等有重要影响.为探究bHLH在丹参酮合成中的作用,本研究通过基因克隆获得丹参bHLH家族基因SmbHLH59 的全长编码序列,并对其进行生物信息学和表达特征分析.结果表明,SmbHLH59 结构保守,含有 3 个外显子和 2 个内含子.SmbHLH59 蛋白由 226 个氨基酸组成,呈弱酸性,疏水性较强,属脂溶性蛋白,稳定性差,无规则卷曲数量多,复杂性较高,亚细胞定位于细胞核,与一串红的bHLH126 亲缘关系最近.SmbHLH59 的启动子区域富含响应植物激素的顺式作用元件.表达分析显示SmbHLH59 在丹参红根韧皮部中表达量最高,受茉莉酸甲酯诱导上调表达,推测该基因与红根中丹参酮的合成有关且其作用受到茉莉酸甲酯的调控.本研究结果可为深入研究SmbHLH59 基因的功能奠定重要基础.

Tanshinones are the primary bioactive compounds in Salvia miltiorrhiza,and their biosynthetic pathways are regulated by various factors.The basic helix-loop-helix(bHLH)transcription factor family plays crucial roles in plant growth metabolism,secondary metabolite synthesis,and stress responses.To explore the role of bHLH in tanshinone biosynthesis,the full-length coding sequence(CDS)of SmbHLH59 was cloned from S.miltiorrhiza,followed by comprehensive bioinformatics and expression profile analyses.The results showed that SmbHLH59 was conserved in structure,containing three exons and two introns.The SmbHLH59 protein was composed of 226 amino acids with weak acidity and highly hydrophobicity,and was a lipophilic protein.It was characterized by low stability,a high proportion of random coils,and high complexity.Subcel-lular localization predicted that SmbHLH59 was located in the nucleus.It had the closest relationship with bHLH126 from Citrus splendens.The promoter region of SmbHLH59 was enriched with cis-acting elements re-sponse to phytohormones.Expression analysis revealed that SmbHLH59 reached the highest expression level in phloem of the red roots and was significantly up-regulated when induced by methyl jasmonate(MeJA),which suggested that SmbHLH59 was involved in tanshinone biosynthesis in the red roots and was regulated by MeJA.This study could provide a vital foundation for further functional characterization of the SmbHLH59 gene.

刘聪;王朝阳;柳江彬;梅显贵;王臣臣;任振丽;宋振巧

山东农业大学农学院,山东 泰安 271018山东农业大学农学院,山东 泰安 271018山东农业大学农学院,山东 泰安 271018山东农业大学农学院,山东 泰安 271018山东丹红制药有限公司,山东 菏泽 274000山东丹红制药有限公司,山东 菏泽 274000山东农业大学农学院,山东 泰安 271018

农业科技

丹参bHLH转录因子基因克隆生物信息学分析表达分析

Salvia miltiorrhizabHLH Transcription factorGene cloningBioinformatics analysisEx-pression analysis

《山东农业科学》 2026 (1)

1-7,7

国家自然科学基金项目(82373991)山东省重点研发计划项目(2023TZXD085)

10.14083/j.issn.1001-4942.2026.01.001

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