Suppr超能文献

[丹参4-羟基-3-甲基-丁-2-烯基二磷酸还原酶基因(smHDR)的克隆及诱导表达分析]

[Cloning and induced expression analysis of 4-hydroxy-3-methyl-but-2-enyl diphosphate reductase gene (smHDR) of Salvia miltiorrhiza].

作者信息

Cheng Qi-Qing, He Yun-fei, Li Geng, Jiang Chao, Yuan Yuan, Gao Wei, Huang Lu-Qi

机构信息

School of Traditional Chinese Medicine, Capital Medical University, Beijing 100069, China.

出版信息

Yao Xue Xue Bao. 2013 Feb;48(2):236-42.

Abstract

This study reported the obtainment of the full-length cDNA of Salvia miltiorrhiza hairy roots (Abbr: SmHDR, GenBank number: JX233817), via extracting Salvia miltiorrhiza hairy roots total RNA, designing specific primers according to the transcriptome data and using the RACE strategy, and then analyzed it with bioinformatics approaches. On this basis, using the real-time PCR to detect SmHDR gene expression after Ag+ induction, and testing tanshinones contents of corresponding samples by UPLC. SmHDR has 1 647 nucleotides, and an open reading frame (ORF) encoding a protein of 463 amino acid residues. The deduced protein has isoelectric point (pI) of 5.72 and a calculated molecular weight about 51.88 kD. In the secondary structure, the percentage of alpha helix, beta turn and random coil were 35.64%, 20.30% and 44.06%, respectively. Sequence alignment and phylogenetic analysis demonstrated that SmHDR had relative close relationship to the HDR of Picrorhiza kurrooa, similar to HDR from other species of plants. Real time PCR results indicated that elicitor of Ag+ stimulated the increase of mRNA expression of SmHDR. At the same time, results of ultra performance liquid chromatography (UPLC), used to examine the accumulation of diterpenoid tanshinones in hairy roots, showed that the contents of diterpenoid tanshinones in hairy roots of Salvia miltiorrhiza were increased dramatically at 12 h after treated with Ag+, and then decreased significantly. This result showed a positive correlation between the levels of mRNA expression and tanshinones accumulation in Salvia miltiorrhiza stimulated by Ag+. The content of tanshinones was gradually raised, and it had an obvious increase at 120 h. The bioinformatics analysis and gene expression indicated that SmHDR might be involved in tanshinones biosynthesis, which laid the foundation for further study of secondary metabolic regulation mechanism of tanshinones.

摘要

本研究报道了通过提取丹参毛状根总RNA,根据转录组数据设计特异性引物并采用RACE策略,获得丹参毛状根全长cDNA(简称:SmHDR,GenBank编号:JX233817),然后用生物信息学方法对其进行分析。在此基础上,利用实时荧光定量PCR检测Ag⁺诱导后SmHDR基因的表达,并通过超高效液相色谱法检测相应样品的丹参酮含量。SmHDR含有1647个核苷酸,一个编码463个氨基酸残基的开放阅读框(ORF)。推导的蛋白质等电点(pI)为5.72,计算分子量约为51.88 kD。在二级结构中,α螺旋、β转角和无规卷曲的比例分别为35.64%、20.30%和44.06%。序列比对和系统发育分析表明,SmHDR与胡黄连的HDR亲缘关系相对较近,与其他植物物种的HDR相似。实时荧光定量PCR结果表明,Ag⁺诱导剂刺激了SmHDR mRNA表达的增加。同时,用于检测毛状根中二萜类丹参酮积累的超高效液相色谱(UPLC)结果表明,丹参毛状根在Ag⁺处理12 h后二萜类丹参酮含量显著增加,然后显著下降。该结果表明,Ag⁺刺激的丹参中mRNA表达水平与丹参酮积累之间呈正相关。丹参酮含量逐渐升高,在120 h时有明显增加。生物信息学分析和基因表达表明,SmHDR可能参与丹参酮的生物合成,为进一步研究丹参酮次生代谢调控机制奠定了基础。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验