期刊文献+

水杨酸·甲基茉莉酸与伤诱导对烟草sm-Nvas同源基因表达调控的初步研究

Effects of Salicylic Acid,Methyl Jasmonate and Wound Induction on the Expression of sm-Nvas Homologous Genes in Tobacco
下载PDF
导出
摘要 [目的]研究Nicotiana sylvestris和Nicotiana attenuata这2种烟草中sm-Nvas同源基因分别在经水杨酸(SA)、甲基茉莉酸(MeJA)及伤诱导后的表达情况。[方法]采用Trizol法提取经水杨酸、甲基茉莉酸及伤处理后的2种烟草叶片的总RNA,转录成cDNA,利用实时荧光定量PCR检测sm-Nvas同源基因的表达量并进行数据分析。[结果]通过对烟草叶片中sm-Nvas同源基因的表达量分析,结果表明水杨酸、甲基茉莉酸及伤处理能对sm-Nvas同源基因的表达起调控作用。[结论]用SA、MJA和伤处理Nicotiana sylvestris和Nicotiana attenuata烟草,发现sm-Nvas的表达量均有所增加。在处理8 h后其表达量发生了明显的变化,在12~16 h其表达量的增加达到峰值。这对研究烟草的sm-Nvas及其同源基因的功能奠定重要的基础。 [Objective]To study the expression of sm-Nvas homologous genes in two tobaccos,Nicotiana sylvestris and Nicotiana attenuata,after salicylic acid(SA),methyl jasmonate(MeJA) and wounding induction,respectively.[Method]Total RNA was extracted from the two tobacco leaves treated with SA,MeJA and wounding using Trizol method,and then reverse transcribed into cDNA.The expression of sm-Nvas homologous gene was detected by real-time fluorescence quantitative PCR and the data were analyzed.[Result]Based on analysis of the expression level of sm-Nvas homologous genes in tobacco leaves,it showed that salicylic acid,methyl jasmonic acid and wound treatment could regulate the expression of sm-Nvas homologous genes.[Conclusion]After SA,MJA and wounding treatment of Nicotiana sylvestris and Nicotiana attenuata tobacco,the expression of sm-Nvas homologous gene increased.After 8 hours of treatment,all the expression levels changed significantly,and reached the peak at about 12-16 hours.This will lay an important foundation for studying the function of sm-Nvas and its homologous genes in tobacco.
作者 邵敏敏 何福收 陈同 王春台 谭艳平 SHAO Min-min;HE Fu-shou;CHEN Tong(School of Life Sciences,South-Central University for Nationalities,Hubei Provincial Key Laboratory of Characteristic Plant Germplasm Protection and Utilization in Wuling Mountains,State Key Laboratory of Biotechnology,Wuhan,Hubei 430074)
出处 《安徽农业科学》 CAS 2020年第16期105-108,150,共5页 Journal of Anhui Agricultural Sciences
基金 湖北省自然科学基金项目(2018CFB481) 中南民族大学研究生学术创新基金项目(2019sycxjj237)。
关键词 甲基茉莉 水杨酸 伤害处理 实时荧光定量PCR sm-Nvas 同源基因 烟草 Methyl jasmonic acid Salicylic acid Injury treatment Real-time PCR sm-Nvas Homologous genes Tobacco
  • 相关文献

参考文献3

二级参考文献29

  • 1袁磊,刘学群,王春台.受MeJA诱导的烟草GTs基因启动子的克隆及转化[J].湖北农业科学,2006,45(6):700-702. 被引量:1
  • 2李静,刘学群,王春台.一个烟草葡糖基转移酶基因启动子的克隆与诱导表达[J].华中农业大学学报,2007,26(3):277-282. 被引量:5
  • 3SHARMA L K,MADINA B M,CHATURVEDI P,et al. Molecular cloning and characterization of one member of 3 betahydroxy sterol glucosyltransferase gene family in Withania somnifera [J]. Arch Biochem Biophy, 2007,460 (1) : 48-55.
  • 4LIME K, BOWLES D J. A class of plant glycosyltransferases involved in cellular homeostasis[J]. EMBO J, 2004, 23: 2915- 2922.
  • 5KUBO A, ARAI Y, NAGASHIMA S, et al. Alteration of sugar donor specificities of plant glycosyltransferases by a single point mutation[J]. Arch Biochem Biophys, 2004,429 : 198-203.
  • 6HE X Z, WANG X, DIXON R A. Mutational analysis of the Medicago glycosyltransferase UGTT1G1 reveals residues that control regioselectivity for (iso)flavonoid glycosylation[J]. J Biol Chem, 2006,281 : 34441-34447.
  • 7MODOLO L V, BLOUNT J W, ACHNINE L, et al. A functional genomics approach to (iso) flavonoid glycosylation in the model legume Medicago truncatula [J]. Plant Mol Biol, 2007, 64:499-518.
  • 8SARAH A O, SOREN B, IMBERTY A, et al. Catalytic key amino acids and UDP-sugar donor specificity of a plant glucuronosyltransferase, UGT94B1 : molecular modeling substantiated by site-specific mutagenesis and biochemical analyses[J]. Plant Physiol, 2008,148 : 1295-1308.
  • 9THORSOE K S,BARK S,OLSEN C E,et al. Determination of catalytic key acids and UDP sugar donor specificity of the cyanohydrin glycosyltransferase UGT85B1 from Sorghum bicolor : molecular modeling substantiated by site-specific mutagenesis and biochemical analysesDJ. Plant Physiol, 2005,139; 664- 673.
  • 10STANLEY P. Regulation of notch signaling by glycosylation [J]. Curr Opin Struct Biol, 2007,17(5) : 5ao-535.

共引文献3

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