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园艺学报 ›› 2010, Vol. 37 ›› Issue (8): 1295-1302.

• 观赏植物 • 上一篇    下一篇

牡丹查耳酮合酶基因Ps-CHS1的克隆及其组织特异性表达

周 琳,王 雁*,彭镇华   

  1. (中国林业科学研究院林业研究所,国家林业局林木培育重点实验室,北京 100091)
  • 收稿日期:2010-03-13 修回日期:2010-07-15 出版日期:2010-08-25 发布日期:2010-08-25
  • 通讯作者: 王 雁

Isolation and Tissue-specific Expression of Chalcone Synthase Gene Ps-CHS1 in Tree Peony

ZHOU Lin,WANG Yan*,and PENG Zhen-hua   

  1. (Key Laboratory of Tree Breeding and Cultivation,State Forestry Administration,Research Institute of Forestry,Chinese Academy of Forestry,Beijing 100091,China)
  • Received:2010-03-13 Revised:2010-07-15 Online:2010-08-25 Published:2010-08-25
  • Contact: WANG Yan

摘要: 以牡丹(Paeonia suffruticosa)品种‘彩绘’为试材,采用RT-PCR和RACE方法从花瓣中获得了一个牡丹查耳酮合酶(chalcone synthase,CHS)基因cDNA全长,命名为Ps-CHS1,GenBank登录号为GQ483511。序列分析结果表明,Ps-CHS1全长1 475 bp,包含82 bp的5′非编码区、208 bp的3′非编码区和一个长度为1 185 bp编码394个氨基酸的开放阅读框。氨基酸序列分析显示该基因编码的蛋白具有CHS家族保守存在的所有功能活性位点和特征多肽序列。序列比对和系统进化分析表明,Ps-CHS1与杨柳科、锦葵科、蔷薇科等植物的CHS亲缘关系较近,相似性达90%以上。相对荧光定量PCR分析表明,Ps-CHS1在花瓣中的表达量最高,其次是萼片,再次是叶片和雄蕊,在心皮中表达量最低。

关键词: 牡丹, 查耳酮合酶基因, 相对荧光定量PCR, 组织特异性表达

Abstract: In this work,a full-length cDNA sequence of chalcone synthase(CHS)gene was obtained from petals of Paeonia suffruticosa‘Caihui’using RT-PCR and RACE,named Ps-CHS1(GenBank accession No. GQ483511). Sequence analysis indicated that Ps-CHS1 is 1 475 bp in full length and contains a 5′-untranslated region(5′-UTR)of 82 bp,a 3′-UTR of 208 bp,and an opening reading frame(ORF)of 1 185 bp encoding a 394 predicted amino acids residues which possessed all the conserved active sites for the CHS function as well as the family signature. Sequence alignment and phylogenetic analysis revealed that Ps-CHS1 shared more than 90% homology with CHS from plants in Salicaceae,Malvaceae and Rosaceae. Relative real-time PCR analysis indicated that Ps-CHS1 showed the highest transcript abundance in petals,moderate levels in sepals,low levels in leaves and stamens and the lowest levels in carpels.

Key words: tree peony, Paeonia suffruticosa, chalcone synthase gene, relative real-time PCR, tissue-specific expression

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