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棉花4个脂肪酸合成相关基因的克隆和表达特征分析 被引量:4

Molecular Cloning and Expression Analysis of Four Novel Fatty Acid Synthesis Related Genes in Gossypium hirsutum L.
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摘要 脂肪酸合成相关代谢在控制油的合成和抗非生物胁迫中均起着重要作用,其脂肪酸合成相关基因的时空表达水平直接影响油的含量和脂肪酸合成相关酶的活性。本研究克隆了4个脂肪酸合成相关基因,分别命名为GhKASII、GhKASIII、GhFAD和GhGPAT,其中GhKASIII、GhFAD和GhGPAT基因cDNA全长通过电子克隆和同源克隆得到。而GhKASII通过筛库和5′RACE途径得到。组织表达分析表明,上述4个基因在根、茎、叶及纤维发育不同时期均有表达,属于组成性表达基因。其中GhKASII、GhKASIII在25 DPA种子中表达量最高,GhGPAT在0 DPA胚珠和15 DPA纤维中表达量很高,GhFAD在0 DPA胚珠,15 DPA种子,20 DPA纤维中表达量均很高。不同非生物胁迫的诱导表达分析表明,上述4个基因均不同程度被茉莉酸甲酯,ABA,创伤和冷害等逆境诱导表达。 Metabolism related to fatty acid synthesis plays an important role both in regulating oil biosynthesis and in plant abiotic stress tolerance.The spatial and temporal expression level of genes related to fatty acid synthesis influences the oil content and enzymes activity for fatty acid synthesis.In this study,four novel genes related to fatty acid synthesis,designated GhKASII,GhKASIII,GhFAD,and GhGPAT,were first isolated from upland cotton,respectively.The cDNA full-length of GhKASIII,GhFAD and GhGPAT were obtained by combining homologic cloning and in sillico cloning,while GhKASII was obtained by screening cDNA library and 5′RACE technique.The expression pattern analysis of different tissues and organs revealed that the transcripts of these genes were widely distributed in all the tested tissues and organs.GhKASII and GhKASIII showed the highest expression level in seeds at 25 DPA(days post anthesis),however,GhGPAT in 0 DPA ovules and 15DPA fiber tissues and GhFAD in 0 DPA ovules,15 DPA seeds and 20 DPA fibers,respectively.Further,the analysis of expression induced by abiotic treatments indicated that the genes were differentially regulated under wounding,methyl jasmonate(MeJA),cold and ABA(abscisic acid) treatments.The study will pave a way to develop further research in oil improvement of cotton seed and resistance to abiotic stress in cotton.
出处 《作物学报》 CAS CSCD 北大核心 2010年第12期2084-2090,共7页 Acta Agronomica Sinica
基金 国家重大基础研究计划项目(973计划)(2007CB108805) 教育部高等学校学科创新引智计划项目(111计划)(B08025)资助
关键词 脂肪酸合成 克隆 表达 非生物胁迫 陆地棉 Fatty acid synthesis Cloning Expression Abiotic stress Upland cotton
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参考文献17

  • 1Seki M, Kamei A, Shinozaki K Y. Molecular responses to drought, salinity and frost: common and different paths for plant protection. Curr Opin Biotechnol, 2003, 14:194-199.
  • 2Pirfle I L, Kongcharoensuntom W, Nampaisansuk M, Knesek J E, Chapman K D, Pirtle R M. Molecular cloning and functional expression of the gene for a cotton A12 fatty acid desaturase (FAD2). Biochim Biophys Acta, 2001, 2:122-129.
  • 3Wolter F P, Schrnidt R, Heinz E. Chilling sensitivity of Arabidopsis thaliana with genetically engineered membrane lipids. EMBO J, 1992, 11:4685-4692.
  • 4Ohlrogge J B, Kuhn D N, Stumpf P K. Subcellular localization of acyl cartier protein in leaf protoplasts of Spinacia oleracea. Proc Natl Acad Sci USA, 1979, 76:1194-1198.
  • 5Anal T, Koga M, Tanaka H, Kinoshita T, Rahman S M, Takagi Y. Improvement of rice (Oryza sativa L.) seed oil quality through introduction of a soybean microsomal omega-3 fatty acid desaturase gene. Plant Cell Rep, 2003, 21:988-992.
  • 6武耀廷,刘进元.一种高效提取棉花不同组织总RNA的热硼酸改良法[J].棉花学报,2004,16(2):67-71. 被引量:42
  • 7蒋建雄,张天真.利用CTAB/酸酚法提取棉花组织总RNA[J].棉花学报,2003,15(3):166-167. 被引量:141
  • 8Livak K J, Schrnittgen T D. Analysis of relative gene expression data using real-time quantitative PCR and the 2(-delta delta C(T)) method. Methods, 2001, 25:402-408.
  • 9Hwang S K, Hwang Y S. Molecular cloning and functional expression of Perilla frutescens 3-ketoacyl-[acyl cartier protein] synthase III. Mol Cells, 2000, 10:375-381.
  • 10Hwang S K, Kim K H, Hwang Y S. Molecular cloning and expression analysis of 3-ketoacyl-acp synthases in the immature seeds of Perillafrutescens. Mol Cells, 2000, 10:533-539.

二级参考文献20

  • 1PATERSON A H, Brubaker C L, Wendel J F. A rapid method for extraction of cotton (Gossipium spp. ) genomic DNA suitable for RFLP and PCR analysis [J]. Plant Mol Biol Rep, 1993, 11: 122-127.
  • 2FANG G, Hammar S, Grumet R. A quick and inexpensive method for removing polysaccharides from plant genomic DNA [J]. Biotechniques, 1992, 13: 52-56.
  • 3SU X, Gibor A. A method for RNA isolation from marine macro-algae [J]. Anal Biochern, 1988, 174:650-657.
  • 4黄培堂 J.萨姆布鲁克D.W.拉赛尔.分子克隆实验指南(第三版)[M].,2002.26-27,96-99.
  • 5JOHN M E. An efficient method for isolation of RNA and DNA from plants containing polyphenolics[J].Nucleic Acids Res, 1992, 20:2381.
  • 6SCHNEIDERBAUER A, Sandermann H Jr, Emst D.Isolation of functional RNA from plant tissues rich in phenolic compounds[J]. Anal Biochem, 1991 (197):91-95.
  • 7LEWINSOHN E, Steele C L, Croteau R. Simple isolation of functional RNA from woody stems of gymnosperms[J]. Plant Mol Bio Rep, 1994(12): 20-25.
  • 8BAKER S S, Rugh C L, Kamalay J C. RNA and DNA isolation from recalcitrant plant tissues[J]. Bio Techniques, 1990(9) :268-272.
  • 9HUGHES D W, Galau G. Preparation of RNA from cotton leaves and pollen[J]. Plant Mol Bio Rep, 1988(6) :253-257.
  • 10WAN C Y, Wilkins T A. A modified hot borate method significantly enhances the yield of high-quality RNA from cotton(Gossypium hirsutum L. )[J]. Anal Biochem, 1994(223) :7-12.

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