Li Jun, Long Deng-Kai, Li Jun, Zhou Tao, Zheng Wei, Ding Ling, Jiang Wei-Ke
Guiyang University of Chinese Medicine, Guiyang 550002, China.
Zhongguo Zhong Yao Za Zhi. 2016 Jul;41(13):2404-2410. doi: 10.4268/cjcmm20161306.
To investigate the molecular mechanism of quality formation of Pseudostellaria heterophylla, the carotenoid cleavage dioxygenases (CCDs) genes were cloned from the transcriptome database of P. heterophylla, and analyzed them with bioinformatics analysis and expression analysis. The sequence length of four new gene were 1 617, 1 461, 1 746, 1 875 bp, and subsequently, named as PhCCD1,PhNCED2,PhNCED3 and PhCCD4 according to its genetic relationship with Arabidopsis thaliana. The sequence analysis showed that four new gene were all containing REP65 domains and binding sites of ferrous ion, such as histidine, glutamates and aspartates. Analysis phylogeny showed that PhNCED2 and PhNCED3 were the cluster of NCEDs, PhCCD1 and PhCCD4 were the cluster of CCDs. In addition, PhCCD1 and AtCDD1 of Arabidopsis thaliana, PhCCD4 and AtCCD4 of A. thaliana,PhNCED2, PhNCED3 and AtNCED3 of A. thaliana have high similarities. Analysis of real-time fluorescence quantitative showed that PhNCED2 and PhNCED3 were expressed mainly in underground part, the expression quantity of PhNCED2 reached the highest in fibrous root, PhNCED3 keeps higher in phloem and xylem, it may be the key enzymes of ABA biosynthesis genes. Moreover,PhCCD1 and PhCCD4 were expressed mainly in aerial part,the expression quantity of PhCCD1 reached the highest in leaf,PhCCD4 keeps higher in stem and leaf.It may be involved in the biosynthesis of carotenoids for P. heterophylla. The study obtained CDDs gene of P. heterophylla for the first time,this would lay the foundation of developing the response mechanism of P. heterophylla about external stress further,and then exploring the biological approach of quality formation in P. heterophylla.
为研究太子参品质形成的分子机制,从太子参转录组数据库中克隆类胡萝卜素裂解双加氧酶(CCDs)基因,并进行生物信息学分析和表达分析。4个新基因的序列长度分别为1617、1461、1746、1875 bp,随后根据其与拟南芥的亲缘关系分别命名为PhCCD1、PhNCED2、PhNCED3和PhCCD4。序列分析表明,4个新基因均含有REP65结构域以及亚铁离子结合位点,如组氨酸、谷氨酸和天冬氨酸。系统发育分析表明,PhNCED2和PhNCED3属于NCEDs聚类,PhCCD1和PhCCD4属于CCDs聚类。此外,太子参的PhCCD1与拟南芥的AtCDD1、太子参的PhCCD4与拟南芥的AtCCD4、太子参的PhNCED2、PhNCED3与拟南芥的AtNCED3具有较高的相似性。实时荧光定量分析表明,PhNCED2和PhNCED3主要在地下部分表达,PhNCED2在须根中表达量最高,PhNCED3在韧皮部和木质部中保持较高表达,可能是脱落酸生物合成基因的关键酶。此外,PhCCD1和PhCCD4主要在地上部分表达;PhCCD1在叶片中表达量最高,PhCCD4在茎和叶中保持较高表达,可能参与太子参类胡萝卜素的生物合成。该研究首次获得太子参的CCDs基因,这将为进一步揭示太子参对外界胁迫的响应机制奠定基础,进而探索太子参品质形成的生物学途径。