生物技术通报 ›› 2023, Vol. 39 ›› Issue (3): 206-217.doi: 10.13560/j.cnki.biotech.bull.1985.2022-0532

• 研究报告 • 上一篇    下一篇

滇牡丹PdANS的克隆、表达及与花青素含量的相关性

平怀磊1(), 郭雪2, 余潇2, 宋静2, 杜春1, 王娟3(), 张怀璧4   

  1. 1.西南林业大学林学院,昆明 650224
    2.西南林业大学园林园艺学院,昆明 650224
    3.西南林业大学绿色发展研究院,昆明 650224
    4.新西兰皇家植物与食品研究所,北帕默斯顿 11600
  • 收稿日期:2022-04-29 出版日期:2023-03-26 发布日期:2023-04-10
  • 通讯作者: 王娟,女,博士,教授,博士生导师,研究方向:生物多样性保护、植物学、生态学;E-mail:Schima@163.com
  • 作者简介:平怀磊,男,硕士研究生,研究方向:生物多样性保护与利用;E-mail:2681418377@qq.com
  • 基金资助:
    云南省重大基础专项生物资源数字化开发应用项目(202002AA100007);国家自然科学基金项目(32060089);云南省万人计划“云岭产业技术领军人才”专项(云发改[2018]212 号);云南省千人计划专项(2019)

Cloning and Expression of PdANS in Paeonia delavayi and Correlation with Anthocyanin Content

PING Huai-lei1(), GUO Xue2, YU Xiao2, SONG Jing2, DU Chun1, WANG Juan3(), ZHANG Huai-bi4   

  1. 1. Faculty of Forestry, Southwest Forestry University, Kunming 650224
    2. College of Landscape Architecture and Horticulture Sciences, Southwest Forestry University, Kunming 650224
    3. Eco-Development Academy of Southwest Forestry University, Kunming 650224
    4. New Zealand Institute for Plant & Food Research Limited, Palmerston North 11600, New Zealand
  • Received:2022-04-29 Published:2023-03-26 Online:2023-04-10

摘要:

花色是观赏植物最重要的品质性状之一,在植物生长发育过程中发挥着重要作用。探明滇牡丹的花色调控机理,为提高观赏价值奠定理论基础。以花瓣为材料,克隆获得PdANS,生物信息学分析其特征,结合实时荧光定量PCR、HPLC等技术探究不同组织、不同发育时期中PdANS的表达情况与各组织花青素含量的相关性。结果表明,PdANS全长1 121 bp,包含一个1 064 bp的开放阅读框(ORF),编码354个氨基酸,相对分子质量40.41 kD,理论等电点(pI)5.48,分子式为C1819H2876N474O540S12,脂肪指数为88.64,不稳定指数(II)为55.32,亲水平均数为-0.435,推测为不稳定的亲水蛋白。且无信号肽序列及跨膜螺旋区,是没有分泌功能的非跨膜蛋白。系统进化分析显示,滇牡丹PdANS与牡丹、芍药等植物的ANS蛋白亲缘关系最近。RT-qPCR结果显示,PdANS在花瓣、花药、萼片、苞片和花梗中均有表达,以花瓣中的表达量最高。HPLC结果表明,在不同组织提取液中,分别检测出Cy3G5G、Pn3G5G、Cy3G和Pn3G四种花青素,且花青素含量花瓣>花药>萼片>花梗>苞片。相关性分析表明,花青素含量与PdANS表达量呈极显著相关性。推测PdANS在滇牡丹花色的形成中扮演着重要角色,参与花青素物质的生物合成。

关键词: 滇牡丹, ANS基因, 花青素, 生物信息学分析, HPLC

Abstract:

Flower color is one of the most important quality traits of ornamental plants and plays an important role in the process of plant growth and development. Exploring the mechanism of flower colors regulation in Paeonia delavayi lays the theoretical foundation for improving the ornamental value. The petals were used as the material to clone PdANS, using bioinformatics ally to analyze its characteristics, and combined with real-time fluorescence quantitative PCR and HPLC to investigate the correlation between the expressions of PdANS in different tissues, different developmental periods and the anthocyanin content of each tissue. The results showed that the full length of PdANS was 1 121 bp, including an open reading frame(ORF)of 1 064 bp, encoding 354 amino acids, the relative molecular mass was 40.41 kD, the theoretical isoelectric point(pI)was 5.48, the molecular formula was C1819H2876N474O540S12, the aliphatic index was 88.64, the instability index(II)was 55.32, and the average hydrophilicity was -0.435. It was presumed that it was an unstable hydrophilic protein. And there was no signal peptide sequence and transmembrane helix region, which was a non-transmembrane protein without secretory function. The phylogenetic analysis showed that PdANS of P. delavayi was most closely related to the ANS proteins of P. suffruticosa, Paeonia lactiflora and other plants. The results of the RT-qPCR revealed that PdANS was expressed in the petals, anthers, sepals, bracts and pedicels, with the highest expression in petals. The results of HPLC showed that Cy3G5G, Pn3G5G, Cy3G and Pn3G were detected in the extracts of different tissues, with the content of the anthocyanin of petals > anthers > sepals > pedicels > bracts. The correlation analysis showed that the anthocyanin contents were highly significantly correlated with the expression of PdANS. It is speculated that PdANS plays an important role in formation of flower color in P. delavayi and is involved in the biosynthesis of anthocyanin substances.

Key words: Paeonia delavayi, ANS gene, anthocyanin, bioinformatics analysis, HPLC