斑地锦黄烷酮3羟化酶基因及启动子的克隆与分析
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江西省抚州市指导性科技计划(FKZ2020003)


Cloning and Analysis of Flavanone 3hydroxylase Gene and Its Promoter from Euphorbia maculata L.
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    摘要:

    该研究以斑地锦茎叶为材料,利用同源克隆结合RACE和TailPCR法,克隆了1个黄烷酮3羟化酶(F3H)基因,命名为EmF3H(GenBank登录号为MW767838),其ORF区为1 092 bp,编码364个氨基酸。生物信息学分析显示,EmF3H蛋白相对分子质量为40.93 kD,等电点为5.47,属于2酮戊二酸铁依赖的双加氧酶超家族,其氨基酸序列与油桐的序列相似性为85.5%,在系统进化上为相对独立的一个分支。采用TailPCR法获得1 604 bp的EmF3H启动子序列,分析发现其内含TAATbox、CAATbox等序列和Gbox等光反应元件。qRTPCR结果表明,EmF3H基因在不同生长期各组织中均有表达,其中花期的根和果期的果实中表达水平最高。此结果为进一步研究EmF3H基因表达调控奠定了基础,也为完善斑地锦槲皮素生物合成途径提供了新思路。

    Abstract:

    In this study, a flavanone 3hydroxylase (F3H) gene named EmF3H (GenBank: MW767838) was cloned from Euphorbia maculata with homologous cloning, RACE technology and TailPCR. The ORF of EmF3H is 1 092 bp, encoding 364 amino acids. Bioinformatics analysis showed that the theoretical molecular weight of EmF3H protein is 40.93 kD, theoretical pI is 5.47 and EmF3H protein belongs to 2oxoglutaratede pendent dioxygenase protein family. EmF3H protein is 85.5% similar to VfF3H (ARV78456.1) and located on the independent evolutionary node in phylogenetic tree. The 1 604 bp sequence of EmF3H promoter was cloned by TailPCR and included TAATbox, CAATbox, light responsive element and so on. The analysis of realtime quantitative PCR indicated that EmF3H gene was expressed among different tissues during different growth periods, with the strongest expression in the roots at the flowering stage and the fruits at fruiting stage. These results will provide a foundation for further research on gene expression regulation of EmF3H gene and improving the biosynthesis pathway of quercetin in Euphorbia maculata.

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钟小菊,吴晴阳,张永康,等.斑地锦黄烷酮3羟化酶基因及启动子的克隆与分析[J].西北植物学报,2021,41(9):1475-1481

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  • 在线发布日期: 2021-09-28
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