云南栘[木衣]bHLH22基因克隆及表达OA
Cloning and Expression of bHLH22 Gene from Docynia delavayi
bHLH 转录因子在植物生长发育及抗逆过程中发挥着极为关键的调控作用,为进一步研究 bHLH 转录因子在云南栘[木衣](Docynia delavayi(Franch.)Schneid.)中的表达特征和作用机制,以全基因组、转录组与代谢组多组学联合分析筛选获得的果实香气物质合成关键基因 DdebHLH22 为研究对象,基于其 CDS 序列进行基因克隆,开展生物信息 学 分 析,并采用 RT-qPCR 技术对该基因的组织特异性表达进行了分析.结果表明:Dde-bHLH22 基因的全长 CDS 序列为 744 bp.DdebHLH22 相对分子质量为 27 800.67,编码 243 个氨基酸,理论等电点为 5.58;属于不稳定亲水蛋白,包含 34 个潜在蛋白磷酸化位点,无信号肽及跨膜区域,其二级结构和三级结构的组成以 α 螺旋和无规则卷曲为主;系统进化树构建分析结果显示,云南栘[木衣]与苹果的亲缘关系最近;转录组数据分析表明,DdebHLH22 基因在果实的不同发育阶段以及采摘后的不同贮藏时期表达水平不同,采摘后 S1 期表达水平最高后呈下降趋势;实时荧光定量 PCR 结果显示,DdebHLH22 基因在果实、叶、根、茎中均有表达,在果实中呈现特异性.
The bHLH transcription factors play critical regulatory roles in plant growth,development and stress tolerance.To further explore the expression patterns and functional mechanisms of bHLH transcription factors in Docynia delavayi(Franch.)Schneid.,we selected DdebHLH22,a key gene involved in fruit aroma biosynthesis identified via combined multi-omics analysis of genome,transcriptome and metabolome,as the research material.Gene cloning was performed based on its CDS sequence,followed by bioinformatics analysis.The tissue-specific expression of this gene was also detec-ted using RT-qPCR.The results showed that the full-length CDS of DdebHLH22 was 744 bp.This gene encoded a protein of 243 amino acids with a relative molecular mass of 27 800.67 and a theoretical isoelectric point of 5.58.The protein was predicted to be an unstable hydrophilic protein,containing 34 potential protein phosphorylation sites,with no signal pep-tide or transmembrane domain.Its secondary and tertiary structures were mainly composed of α-helices and random coils.Phylogenetic tree analysis revealed that D.delavayi had the closest genetic relationship with Malus domestica.Transcrip-tome data indicated that the expression level of DdebHLH22 varied across different fruit developmental stages and posthar-vest storage periods,its expression peaked at postharvest stage S1 and then decreased gradually.RT-qPCR results demon-strated that DdebHLH22 was expressed in fruits,leaves,roots and stems,and exhibited fruit-specific expression character-istics.
子凤珍;罗亚敏;刘国平;李菊彩;李智华;王大玮
西南林业大学林学院,昆明,650224西南林业大学林学院,昆明,650224西南林业大学林学院,昆明,650224昆明市西山林场,昆明,650100临沧市林业科学院,临沧||677000西南林业大学林学院,昆明,650224
农业科技
云南栘[木衣]基因克隆基因表达生物信息学分析DdebHLH22基因
Docynia delavayiGene cloningGene expressionBioinformatic analysisDdebHLH22 gene
《东北林业大学学报》 2026 (9)
1-8,8
云南省基础研究重点项目(202401AS070042)国家自然科学基金项目(32460401、32060350)西南林业大学重点学科和重点实验室开放基金项目(LXXK-2023Z01).
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