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作物学报 ›› 2013, Vol. 39 ›› Issue (10): 1739-1745.doi: 10.3724/SP.J.1006.2013.01739

• 作物遗传育种·种质资源·分子遗传学 • 上一篇    下一篇

大豆腺苷酸激酶基因GmADK的克隆与表达分析

盖江涛,赵团结,李艳*,盖钧镒*   

  1. 南京农业大学大豆研究所 / 国家大豆改良中心 / 农业部大豆生物学与遗传育种重点实验室 / 作物遗传与种质创新国家重点实验室,江苏南京210095
  • 收稿日期:2013-01-18 修回日期:2013-05-24 出版日期:2013-10-12 网络出版日期:2013-07-31
  • 通讯作者: 李艳, E-mail: yanli1@njau.edu.cn; 盖钧镒, E-mail: sir@njau.edu.cn
  • 基金资助:

    本研究由国家重点基础研究发展计划(973计划)项目(2011CB1093), 国家自然科学基金项目(31071442), 农业部大豆生物学与遗传育种创新团队, 农业部公益性行业专项(200803060), 江苏省优势学科建设工程专项和国家重点实验室自主课题和国家现代农业产业技术体系建设专项(CARS-04)资助。

Cloning and Expression Analysis of an Adenylate Kinase Gene GmADK in Soybean

GAI Jiang-Tao,ZHAO Tuan-Jie,LI Yan*,GAI Jun-Yi*   

  1. Soybean Research Institute / National Center for Soybean Improvement / MOA Key Laboratory for Biology and Genetic Improvement of Soybean (General) / National Key Laboratory of Crop Genetics and Germplasm Enhancement, Nanjing Agricultural University, Nanjing 210095, China
  • Received:2013-01-18 Revised:2013-05-24 Published:2013-10-12 Published online:2013-07-31
  • Contact: 李艳, E-mail: yanli1@njau.edu.cn; 盖钧镒, E-mail: sir@njau.edu.cn

摘要:

腺苷酸激酶(adenylate kinaseADK)催化ATP+AMP2ADP的可逆反应,是维持细胞能量动态平衡的关键酶,在植物中参与调节生长发育和逆境应答等过程。目前有关大豆ADK的研究还未见报道。本文通过RT-PCR方法,从耐盐大豆品种南农1138-2的叶中克隆到一个腺苷酸激酶基因,命名为GmADKGmADK的编码区序列(coding DNA sequence, CDS)804 bp,编码267个氨基酸。预测其蛋白结构含有典型的腺苷酸激酶功能域ATP-AMP(Ap5A)结合位点和AMP结合位点。蛋白序列比对和进化树分析表明,大豆与菜豆(Phaseolus vulgaris)和蒺藜苜蓿(Medicago truncatula)中的ADK序列相似性最高,亲缘关系最近。组织表达显示GmADK基因的表达量在大豆叶和根中高于茎中。荧光定量PCR分析表明GmADK的表达受盐胁迫的调节,且在耐盐(南农1138-2)和盐敏感(科丰1)品种间存在差异。在叶和根中, 200 mmol L–1 NaCl处理61224 h后,GmADK的表达量在盐敏感品种中比未处理对照有所降低,但在耐盐品种中却比未处理对照升高,因此推测GmADK可能参与大豆对盐胁迫的响应。

关键词: 大豆 (Glycine max (L.) Merr.), 腺苷酸激酶, 基因克隆, 盐胁迫

Abstract:

Adenylate kinase (ADK) is an important enzyme in cellular energy homeostasis, which catalyzes the interconversion of adenine nucleotides, ATP+AMP2ADP, and is involved in many processes including plant growth, development and response to abiotic stresses. To date, there has no report on cloning and expression analysis of soybean ADK gene yet. In this study, a soybean ADK gene was cloned from the leaves of a salt tolerant cultivar NN1138-2 using RT-PCR, and was designated as GmADK. The coding sequence (CDS) of this cloned ADK gene is 804 bp in length, encoding a polypeptide of 267 amino acids. Its protein was predicted to be located in plastids, containing a typical ATP-AMP (Ap5A) binding site and an AMP binding site. Multiple sequence alignments and phytogenetic analysis of ADK proteins showed GmADK is most similar with ADK from Phaseolus vulgarisand Medicago truncatula. Tissue expression pattern of GmADK showed its mRNA was more abundant in soybean roots and leaves than in stems. Quantitative RT-PCR showed a differential expression pattern of GmADK in response to salt between salt tolerant (NN1138-2) and sensitive (Kefeng-1) soybean genotypes. Compared with untreated plants, the expression of GmADK in both leaves and roots was repressed after 6, 12, and 24 hours of 200 mmol L–1 NaCl treatment in the salt sensitive cultivar, but induced in the salt tolerant cultivar, indicating that GmADK might be involved in soybean response to salt stress.

Key words: Soybean (Glycine max [L.] Merr.), Adenylate kinase (ADK), Gene cloning, Salt stress

[1]Tan Z-W(谭志文), Liu J(刘俊), Zhang X-F(张学芳), Meng F-G(孟凡国), Zhang Y-Z(张耀洲). Expression, purification and enzymatic characterization of adenylate kinase of Thermus thermophilus HB27 in Escherichia coli. J Southern Med Univ (南方医科大学学报), 2010, 30(1): 1–6 (in Chinese with English abstract)



[2]Declerck P J, Muller M. Hydrogenosomal ATP:AMP phosphotransferase of Trichomonas vaginalis. Comp Biochem Physiol B, 1987, 88: 575–580



[3]Chen B, Sysoeva T A, Chowdhury S, Guo L, Nixon B T. ADPase activity of recombinantly expressed thermotolerant ATPases may be caused by copurification of adenylate kinase of Escherichia coli. FEBS J, 2009, 276: 807–815



[4]Goldberg R N, Tewari Y B, Bhat T N. Thermodynamics of enzyme-catalyzed reactions—a database for quantitative biochemistry. Bioinformatics, 2004, 20: 2874–2877



[5]Pradet A, Raymond P. Adenine nucleotide ratios and adenylate energy charge in energy metabolism. Annu Rev Plant Biol, 1983, 34: 199–224



[6]Atkinson D E. The energy charge of the adenylate pool as a regulatory parameter. Interaction with feedback modifiers. Biochemistry, 1968, 7: 4030–4034



[7]Schlattner U, Wagner E, Greppin H, Bonzon M. Chloroplast adenylate kinase from tobacco: Purification and partial characterization. Phytochemistry, 1996, 42: 589–594



[8]Ching T M, Crane J M. Adenylate energy pool and energy charge in maturing rape seeds. Plant Physiol, 1974, 54: 748–751



[9]Raymond P, Pradet A. Stabilization of adenine nucleotide ratios at various values by an oxygen limitation of respiration in germinating lettuce (Lactuca sativa) seeds. Biochem J, 1980, 190: 39–44



[10]Birkenhead K, Walker D, Foyer C. The intracellular distribution of adenylate kinase in the leaves of spinach, wheat and barley. Planta, 1982, 156: 171–175



[11]Schlattner U, Wagner E, Greppin H, Bonzon M. Adenylate kinase in tobacco cell cultures: II. Variability and regulation of isoform activity patterns in different cell lines. J Plant Physiol, 1994, 144: 400–409



[12]Kleczkowski L A, Randall D D. Equilibration of adenylates by maize leaf adenylate kinase: effects of magnesium on apparent and true equilibria. J Exp Bot, 1991, 42: 537–540



[13]Regierer B, Fernie A R, Springer F, Perez-Melis A, Leisse A, Koehl K, Willmitzer L, Geigenberger P, Kossmann J. Starch content and yield increase as a result of altering adenylate pools in transgenic plants. Nat Biotechnol, 2002, 20: 1256–1260



[14]Zancani M, Casolo V, Vianello A, Francesco Macr??. Involvement of apyrase in the regulation of the adenylate pool by adenylate kinase in plant mitochondria. Plant Sci, 2001, 161: 927–933



[15]Kawai M, Uchimiya H. Biochemical properties of rice adenylate kinase and subcellular location in plant cells. Plant Mol Biol, 1995, 27: 943–951



[16]Xu B-N(徐柏年), Zhang T-Y(张添元), Luo J-X(罗进贤), Wu Q(吴青), Wu J-X(吴江雪). Expression of ADK Gene and ATP Synthesis in Saccharomyces cerevisiae. Acta Sci Nat Univ Sunyatseni (中山大学学报?自然科学版), 2000, (5): 1–4 (in Chinese with English abstract)



[17]Carrari F, Coll-Garcia D, Schauer N, Lytovchenko A, Palacios-Rojas N, Balbo I, Rosso M, Fernie A R. Deficiency of a plastidial adenylate kinase in Arabidopsis results in elevated photosynthetic amino acid biosynthesis and enhanced growth. Plant Physiol, 2005, 137: 70–82



[18]Peterson T A, Nieman R H, Clark R A. Nucleotide Metabolism in Salt-Stressed Zea mays L. Root Tips: I. Adenine and Uridine Nucleotides. Plant Physiol, 1987, 85: 984–989



[19]Gong P, Zhang J, Li H, Yang C, Zhang C, Zhang X, Khurram Z, Zhang Y, Wang T, Fei Z, Ye Z. Transcriptional profiles of drought-responsive genes in modulating transcription signal transduction, and biochemical pathways in tomato. J Exp Bot, 2010, 61: 3563–3575



[20]Chen H-T(陈华涛), Chen X(陈新), Yu D-Y(喻德跃). Inheritance analysis and mapping quantitative trait loci (QTLs) associated with salt tolerance during seedling growth in soybean. Chin J Oil Crop Sci (中国油料作物学报), 2011, 33(3): 231–234 (in Chinese with English abstract)



[21]Berry M B, Phillips G N Jr. Crystal structures of Bacillus stearothermophilus adenylate kinase with bound Ap5A, Mg2+ Ap5A, and Mn2+ Ap5A reveal an intermediate lid position and six coordinate octahedral geometry for bound Mg2+ and Mn2+. Proteins, 1998, 32: 276–288



[22]Birkenhead K, Walker D, Foyer C H. The intracellular distribution of adenylate kinase in the leaves of spinach, wheat and barley. Planta, 1982, 156: 171–175



[23]Hampp R, Goller M, Ziegler H. Adenylate levels, energy charge, and phosphorylation potential during dark-light and light-dark transition in chloroplasts, mitochondria, and cytosol of mesophyll protoplasts from Avena sativa L. Plant Physiol, 1982, 69: 448– 455



[24]Stitt M, Lilley R M, Heldt H W. Adenine nucleotide levels in the cytosol, chloroplasts, and mitochondria of wheat leaf protoplasts. Plant Physiol, 1982, 70: 971–977



[25]Lange P R, Geserick C, Tischendorf G, Zrenner R. Functions of chloroplastic adenylate kinases in Arabidopsis. Plant Physiol, 2008, 146: 492–504



[26]Zhou S P, Wei S, Boone B, Levy S. Microarray analysis of genes affected by salt stress in tomato. Afr J Environ Sci Technol, 2007, 1: 014–026
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