期刊文献+

家稗丙酮酸磷酸双激酶(PPDK)基因的克隆及序列分析 被引量:12

Cloning and Sequence Analysis of pdk Gene in Echinochloa crusgalli var.frumentacea(Roxb.) W.F.Wight
在线阅读 下载PDF
导出
摘要 为揭示C4植物家稗[Echinochloa crusgallivar.frumentacea(Roxb.)W.F.Wight]PPDK结构和功能特点,探索改善作物高光效途径,采用RT-PCR技术,克隆了家稗丙酮酸磷酸双激酶(PPDK)基因的cDNA全长。核苷酸序列分析表明,该片段全长3 085 bp,包含一个2 844 bp的开放阅读框,编码948个氨基酸(GenBank登录号:AY 792619)。编码区核苷酸序列与高粱(Sorghum bicolor)、甘蔗(Saccharum officinarum)、玉米(Zea mays)等C4型pdk基因同源率分别为85.1%、84.0%和82.0%;与水稻[Oryza sativa(japonicacultivar-group)]pdk基因同源性也高达82.6%。氨基酸序列进化树分析表明,其与玉米、水稻等禾本科植物最为接近。半定量RT-PCR研究表明,pdk基因仅在绿色叶片中表达。 Pyruvate orthophosphate dikinase(PPDK) plays an important role in C4 photosynthesis. In order to elucidate structural and functional characters of PPDK from Echinochloa crusgalli var. frumentacea (Roxb.) W. F. Wight, and search a new approach to improve crop photosynthesis, a full-length cDNA for PPDK was isolated from E. crusgaUi var. frumentacea (Roxb.) W. F. Wight by RT-PCR method. Sequencing analysis showed that the sequence lengtll was 3 085 bp, including one ORF with 2 844 bp which coded a peotide of 948 amino acids. After alignment on ClustalW program, the identities of the cloned fragment with PPDK genes from C4 plants Sorghum bicolor, Saccharum officinarum and Zea mays were about 85.1%, 84.0%, and 82.0% respectively; and that from C3 plant [ Oryza sativa (japonica cultivar-group)] was about 82.6%. The sequence has been submitted to the GenBank database, the accession number is AY792619. Alignment and phylogenetic analysis of the amino acid sequence deduced from the fragment and the PPDK sequences of other plants retrieved from GenBank were carried out by DNAstar program showing the sequence was close to Oryza sativa and Zea mays. Semi-quantitative RT-PCR analysis showed that PPDK was expressed exclusively in leaves.
出处 《作物学报》 CAS CSCD 北大核心 2007年第6期927-930,共4页 Acta Agronomica Sinica
基金 国家自然科学基金项目(30370853)
关键词 家稗 丙酮酸磷酸两激酶 基因克隆 序列分析 Echinochloa crusgalli var. frumentacea (Roxb.) W. F. Wight Pyruvate orthophosphate dikinase Gene cloning Sequence analysis
  • 相关文献

参考文献16

  • 1Trevanion S J, Furbank R T, Ashton A R. NADP-malate dehydrogenase in the C4 plant Flaveria bidentis (Cosense suppression of activity in mesophyll and bundle-sheath cells and consequences for photosynthesis). Plant Physiol, 1997, 113(4):1153-1165
  • 2Ap Rees T, Hill S A. Metabolic control analysis of plant metabolism. Plant Cell Environ, 1994,17(5):587-599.
  • 3Sheen J. Molecular mechanisms underlying the differential expression of maize pyruvate, orthophosphate dikinase genes. Plant Cell, 1991,3(3): 225-245.
  • 4Chastain C J, Fries J P, Vogel J A, Randklev C L, Vossen A P, Dittmer S K, Watkins E E, Fiedler L J, Wacker S A, Meinhover K C, Sarath G, Chollet R. Pyruvate, orthophosphate dikinase in leaves and chloroplasts of C3 plants undergoes light-/dark-induced reversible phosphorylation. Plant Physiol, 2002,128(4):1368-1378.
  • 5Matsuoka M. The gene for pyruvate, orthophosphate dikinase in C4 plants: structure, regulation and evolution. Plant Cell Physiol, 1995,36(6): 937-943.
  • 6Msurice S B Ku, Yuriko K M, Matsuoka M. Evolution and expression of C4 photosynthesis genes. Plant Physiol, 1996,111(4):949-957.
  • 7Matsuoka M. Structure, genetic mapping, and expression of the gene for pyruvate, orthophosphate dikinase from maize. J Biol Chem, 1990,265(28): 16772-16777.
  • 8Zhang L (张丽). Comparison of Photosynthetic Characters and Their Physiological Mechanism in C3 and C4 Crops. MS Dissertation of China Agricultural University, 2004.
  • 9张桂芳,赵明,丁在松,张丽,肖俊涛.稗草磷酸烯醇式丙酮酸羧化酶(PEPCase)基因的克隆与分析[J].作物学报,2005,31(10):1365-1369. 被引量:32
  • 10Zhang G-F(张桂芳). Cloning Key Enzyme Genes of C4 Photosynthesis from Barnyardgrass ( Echinochloa ) and Transformation in Rice (Oryza sativa L.) and Tobacco (Nicotiana tabacum L.). PhD Dissertation of China Agricultural University, 2005.

二级参考文献26

  • 1匡廷云 赵明 卢从明 白克智.Increasing efficiency of light using, raising output of crops[A]..21世纪作物科技与生产发展学术讨论会文集[C].,2002.20-26.
  • 2赵明 赵秀琴 张旭 ErikSacks ReneeLafitte GlennDDimayuga 肖俊涛.Characteristic of photosynthesis form rice distant hybridization progenies and screening high photosynthesis plants[A]..21世纪作物科技与生产发展学术讨论会文集[C].,2002.69-75.
  • 3Toh H, Kawamura T, Izui K. Molecular evolution of phosphoenolpyruv-ate carboxylase. Plant Cell Physiol, 1994, 17: 31-43
  • 4Latzko E, Kelly G J. The many-faced function of phosphoenolpyruvate carboxylase in C3 plants. Physiologie Vegetale, 1983, 21: 805-815.
  • 5Ding Z-S(丁在松). Cloning of C4 phosphoenolpyruvate carboxylase gene from millet(Setaria italica) and sugarcane(Sacharum officinarum) and improvement of photosynthetic efficiency in their transgenic rice. PhD Dissertation, Chinese Academy of Sciences, 2004.
  • 6Svensson P, Blsing O E, Westhoff P. Evolution of C4 phosphoenolpyruvate carboxylase. Archives of Biochem Biophy, 2003,414: 180-188.
  • 7Rao S K, Magnin N C, Reiskind J B, Bowes G. Photosynthetic and other phosphoenolpyruvate carboxylase isoforms in the single-cell, facultative C(4) system of Hydrilla verticillata. Plant Physiol, 2002, 130(2): 876-886.
  • 8Magnin N C, Cooley B A, Reiskind J B, Bowes G. Regulation and localization of key enzymes during the induction of Kranz-less, C4-type photosynthesis in Hydrilla verticillata. Plant Physiol, 1997, 115: 1 681-1 689.
  • 9Voznesenskaya E V, Franceschi V R, Kiirats O, Artyusheva E G, Freitag H, Edwards G E. Proof of C4 photosynthesis without Kranz anatomy in Bienertia cycloptera (Chenopodiaceae). Plant J, 2002, 31: 649-662.
  • 10Cushman J C, Meyer G, Michalowski C B, Schmitt J M, Bohnert H J. Salt stress leads to differential expression of two isogenes of phosphoenolpyruvate carboxylase during Crassulacean acid metabolism induction in the common ice plant. Plant Cell, 1989, 1: 715-725.

共引文献31

同被引文献157

引证文献12

二级引证文献32

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部