期刊文献+

橡胶树5-烯醇式丙酮莽草酸-3-磷酸合成酶基因的克隆及其响应非生物胁迫的表达分析 被引量:6

Cloning and Expression Analysis of 5-Enolpyruvylshikimate-3-phosphate Synthetase Gene Under Abiotic Stress in Hevea brasiliensis
下载PDF
导出
摘要 5-烯醇式丙酮莽草酸-3-磷酸合成酶(EPSPs)是植物合成芳香族氨基酸的一个重要酶,与许多抗逆相关的次生代谢物的合成有关。本研究利用RACE技术从橡胶树热研7-33-97中获得了全长为2 025 bp的HbEPSPS基因cDNA序列,开放阅读框为1 572 bp,编码523个氨基酸;使用ProtParam tool预测该基因编码的蛋白质分子量为56.01 u,等电点(pI)为7.91。该基因由8个外显子和7个内含子构成,全长4 600 bp。实时荧光定量PCR结果表明,HbEPSPS基因在橡胶树叶片、皮、花、胶乳和胚中均表达,其中以叶片中的表达量为最高。激素、干旱、盐和低温等非生物胁迫都能诱导HbEPSPS基因表达量上调,其中茉莉酸甲酯、乙烯和PEG的上调作用最为显著。橡胶树HbEPSPS基因的克隆及其在非生物胁迫下的表达调控研究将为橡胶树抗逆相关的研究提供理论依据。 5-Enolpyruvylshikimate-3-phosphate (EPSPs) synthase is an important enzyme of the shikimate pathway. It is associated with the synthesis of a lot of secondary metabolites related to stress tolerance. In this study, a 2 025 bp HbEPSPS cDNA, containing a 1 572 bp ORF and encoding 523 amino acids, was cloned from CATAS- 73397 by 5' and 3' RACE. Bioinformatics analysis showed that the molecular weight of HbEPSPS protein was 56.01 u and its isoelectrie point was 7.91. The full length of HbEPSPS gene was 4 600 bp, and there were eight exons and seven introns in HbEPSPS gene. The results of qRT-PCR showed that HbEPSPS could express in leaves, bark, flower, latex and embryo, and among these tissues, but the highest expression level of HbEPSPS was in leaves. The expression of HbEPSPS could be induced by hormones, drought, salt and low temperature, and it was significantly up-regulated under MeJA, ETH and PEG stress, respectively. The cloning and expression analysis of HbEPSPS gene under abiotic stress will provide theoretical basis for rubber tree in the abiotic stress research.
出处 《热带作物学报》 CSCD 北大核心 2013年第5期807-814,共8页 Chinese Journal of Tropical Crops
基金 国家天然橡胶产业技术体系(No.CARS-34) 国家自然科学基金项目(No.30960319 No.31271796) 中国热带农业科学院橡胶研究所基本科研业务费专项(No.1630022011002)
关键词 橡胶树 EPSPS 非生物胁迫 莽草酸途径 Hevea brasiliensis EPSPS Abiotic stress Shikimate pathway
  • 相关文献

参考文献19

  • 1Herrmann K M, Weaver L M. The shikimate pathway[J]. AnnualReview of Plant Hiysiology and Plant Molecular Biology,1999,50(1): 473-503.
  • 2Whetten R, Sederoff R. Liiinbiosynthesis[J]. The Plant Cell,1995(7): 1001-1 013.
  • 3Yazaki K, Malsuoka H, imomura K, ci at A novei daik-indudUeprotein, LeDI-2, and its involvement in root-specific secondarymetabolism in Lithospermum erytkrorhizon[J], Plant Hiysiology,2001,125(4): 1 831-1 841.
  • 4NairRB.BastressKL,RueggerM0.etnf.TheArabidopsisthalitmaREDUCEDEPIDERMALFLUORESCENCEIgeneencodes an aldehyde dehydrogenase involved in ferulic acidand ainapic acid biosynthesis[J]. The Plant Cell, 2004, 16(2):544-554.
  • 5Rogers S, Brand L, Holder S,et al. Amplification of the aroAgene from Escherichia coli results in tolerance to die herbicide^yphosate[J]. Applied and Environmental Microbiology, 1983,46(1): 37-45.
  • 6KI扰 H, Musfe^.f Y, Gasser C. Cloning of an Arabidopsisthdiana gene encoding 5 -enolpytuvyUhikimate -3 -phosphatesynthase : Sequence analysis and manipulation to obtain^yphosate-tolerauit plants[] ]. Molecular and General Genetics,1987, 210(3): 437-442.
  • 7Wang Y, Jones J, Weller S, et dl. Expression and stability ofamplified genes encoding 5-enolpyruvylshikimate-3- phosphatesynthase in glyphosate-tol^ant tobacco cells[J]. Plant MolecularBiology, 1991, 17(6): 1 127-1 138.
  • 8Gong Y,Liao Z,Chen M, et al. Characterization of 5-enolpynivylshikimate 3-pkosphate s^nnthase gene from CamptothecaacumincUtjiJ]. Biologia Plantarum, 2006 , 50(4) : 542-550.
  • 9童旭宏,吴玉香,祝水金.陆地棉EPSPS基因的克隆及其组织特异性表达分析[J].棉花学报,2009,21(4):259-264. 被引量:20
  • 10程华,李琳玲,王燕,姜德志,程水源.银杏EPSPS基因克隆及表达分析[J].西北植物学报,2010,30(12):2365-2372. 被引量:10

二级参考文献82

共引文献125

同被引文献117

引证文献6

二级引证文献21

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