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牡丹查耳酮合酶基因Ps-CHS1的克隆及其组织特异性表达 被引量:21

Isolation and Tissue-specific Expression of Chalcone Synthase Gene Ps-CHS1 in Tree Peony
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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1475bp,包含82bp的5′非编码区、208bp的3′非编码区和一个长度为1185bp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。 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.
出处 《园艺学报》 CAS CSCD 北大核心 2010年第8期1295-1302,共8页 Acta Horticulturae Sinica
基金 国家‘863’项目(2006AA100109) 国家林业局‘948’项目(2006-4-C07)
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 tree peony Paeonia suffruticosa chalcone synthase gene relative real-time PCR tissue-specific expression
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  • 1Durbin M L, McCaig B, Clegg M T. 2000. Molecular evolution of the chalcone synthase multigene family in the morning glory genome. Plant Mol Biol, 42: 79- 92. 被引量:1
  • 2Fetter J L, Jez J M, Bowman M E, Dixon R A, Noel J E 1999. Structure of chalcone synthase and the molecular basis of plant polyketide biosynthesis. Nat Struet Biol, 6:775 - 784. 被引量:1
  • 3Goto-Yamamoto N, Wan G H, Masaki K, Kobayashi S. 2002. Structure and transcription of three chalcone synthase genes of grapevine (Ntis vinifera) . Plant Science, 162:867 - 872. 被引量:1
  • 4Han Y Y, Ming F, Wang J W, Wen J G, Ye M M, Shen D L. 2006. Cloning and characterization of a novel chalcone synthase gene from Phalaenopsis hybrida orchid flowers. Russion Journal of Plant physiology, 53 (2): 223 - 230. 被引量:1
  • 5胡可,孟丽,韩科厅,孙翊,戴思兰.瓜叶菊花青素合成关键结构基因的分离及表达分析[J].园艺学报,2009,36(7):1013-1022. 被引量:42
  • 6黄金霞,王亮生,李晓梅,鲁迎青.花色变异的分子基础与进化模式研究进展[J].植物学通报,2006,23(4):321-333. 被引量:38
  • 7Jiang M, Can J S. 2008. Sequence variation of chalcone synthase gene in a spontaneous white-flower mutant of Chinese eabbage-pak-choi. Mol Biol Rep, 35: 507-512. 被引量:1
  • 8Kim S H, Miztmo K, Fujimura T. 2002. Regulated expression of ADP glucose pyrophosphorylase and chalcone synthases during root development in sweet potato. Plant Growth Regul, 38:173 - 179. 被引量:1
  • 9Kreuzaler F, Ragg H, Fautz E, Kuhn D N, Hahlbrock K. 1983. UV-induction of chalcone synthase mRNA in cell suspension cultures of Petrosklinum hortense. Proc Natl Acad Sci USA, 80:2591 - 2593. 被引量:1
  • 10Lanz T, Tropf S, Marner F J, Schroecler J, Schroeder G 1991. The role ofcysteines in polyketide synthases. J Biol Chem, 266 ( 15 ): 9971 - 9976. 被引量:1

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