期刊文献+

小麦高分子量谷蛋白12亚基基因mRNA的定量分析 被引量:1

Quantitative Analysis of the Accumulation of the mRNA Coding High Weight Molecular Glutenin 12 subunit
下载PDF
导出
摘要 利用RT-PCR的方法研究小麦籽粒灌浆期高分子量谷蛋白12亚基基因mRNA的表达水平。东农7742的12亚基在开花后第6天出现mRNA的表达,花后14 d表达量最高。新克旱9的12亚基mRNA的表达出现在开花后第10天,第18天表达量达最高。在籽粒灌浆的各个时期,东农7742的12亚基基因的mRNA的表达量均明显高于新克旱9。 The study was carried out on the mRNA expression level of HMW-GS 12 during grain falling by RT- PCR. The mRNA accumulation of HMW-GS 12 initiated 6 days post- anthesis and reached the peak 14 days post-anthesis in DN 7742 ,and 10 and 14 days,respectively in XKH 9. In the various stages of grain-filling duration,the mRNA expression amount of HMW-GS 12 was higher markedly in the grain of DN 7742 than that of XKH 9.
作者 张薇 胡尚连
出处 《种子》 CSCD 北大核心 2006年第5期35-37,40,共4页 Seed
关键词 高分子量谷蛋白12亚基 MRNA 定量分析 小麦 HMG 12 subunit mRNA Quantitative analysis Wheat
  • 相关文献

参考文献10

  • 1Bartels D.and Thomoson R.D.Synthesis of mRNA coding for abundant endosperm proteins during wheat grain develipment.Plant Science.1986,46:117-125.
  • 2Marks M.D,Lindell J.S,Larkins B.A.Quantitative analysis of the accumulation of Zein mRNA during maize endosperm development.J Biol Chem.1985 Dec 25;260(30):16445-16450.
  • 3蔡马.研究基因转录的RT-PCR技术[J].生物学杂志,2002,19(3):31-34. 被引量:6
  • 4Thellin.O,Zorzi.W,Lakaye.B,Housekeeping genes as internal standards:use and limits.Journal of biotechnology.1999,75:291 -295.
  • 5姚红艳,赵双宜,夏光敏.改良尿素-氯化锂方法提取成熟小麦种子总RNA[J].中国生物工程杂志,2003,23(4):86-88. 被引量:24
  • 6Altenbach.S.B.Quantification of individual low-molecular-weight glutenin subunit transcripts in developing wheat grains by competitive RT-PCR.Theor Appl Genet.1998,97 (3):413-421.
  • 7关林,方宏筠.植物基因工程原理与技术.北京:科学出版社,1998:589-600.
  • 8Aren Reue.MRNA quantitation techniques:considerations for experimental design and application.The journal of nutrition.1998,128 (11):2038 -2044.
  • 9张丽娜,牛吉山,于玲.用半定量RT-PCR方法分析小麦TaMlo-A1c基因的表达[J].西北植物学报,2005,25(7):1368-1371. 被引量:28
  • 10李勇,王玉芝.竞争RT-PCR法定量检测多药耐药基因的表达[J].生物化学与生物物理进展,1998,25(2):144-147. 被引量:4

二级参考文献31

  • 1LingYU,Ji-ShanNIU,Pei-DuCHEN,Zheng-QiangMA,Da-JunLIU.Cloning, Physical Mapping and Expression Analysis of a Wheat Mlo-like Gene[J].Journal of Integrative Plant Biology,2005,47(2):214-222. 被引量:5
  • 2张晓红,张福荣,籍秀娟,李占荣.KB细胞耐药株的建立及其耐药机制的探讨[J].药学学报,1994,29(4):246-251. 被引量:63
  • 3Anlsworth C. Isolation of RNA from floral tissue of Rumex acetosa(sorrel). Plant Mol Biol Reptr, 1994,12 : 198 - 203.
  • 4Sux, Gibor A. A method for RNA isolation from marine macroalgae.Anal Biochem, 1988, 174:650-657.
  • 5Fang G, Hammar S, Grumet R. A quick and inexpensive method for removing polysaccharides from plant genomic DNA. Biotechniques,1992,13:52-56.
  • 6Su X, Gibor A. A method for RNA isolation from marine macroalgae. Anal Biochem, 1988,174:650 - 657.
  • 7Lewinsohn E, Steele CL, Croteau R. Simple isolation of functional RNA from woody stems of gymnosperms. Plant Mol Biol Reptr,1994, 12:20-25.
  • 8Tesniere C, Vayda ME. Mothod for the isolation of high-quality RNA from grape berry tissues without contaminating tannins or carbohydrates. Plant Mol Biol Reptr, 1991, 9:242 - 251.
  • 9Chomczynsky P and Sacchi N. Single-step method of RNA isolation by acid guanidinium thiocyanatc-phenol-chloroform extraction [ J].Anal Biochem, 1987,162( 1 ) : 156 - 159.
  • 10Chen C J,J Biol Chem,1990年,265卷,1期,506页

共引文献58

同被引文献15

引证文献1

二级引证文献29

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