四川农业大学学报 ›› 2001, Vol. 19 ›› Issue (04): 389-393.doi: 10.16036/j.issn.1000-2650.2001.04.020

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两个小麦-黑麦远缘杂交高代抗病株系的贮藏蛋白分析

肖本泽1, 张怀渝2, 任正隆1, 傅体华1   

  1. 1. 四川农业大学 作物遗传育种省级重点实验室, 四川 雅安 625014;
    2. 四川农业大学 基础部, 四川 雅安 625014
  • 收稿日期:2001-09-01 出版日期:2001-12-31 发布日期:2017-03-06
  • 基金资助:
    教育部重点项目基金资助;四川省科技厅应用基础项目资助

Storage Protein Analysis of Two Advanced Resistant Lines Devived from Wheat×Rye Hybrids

XIAO Ben-ze1, ZHANG Huai-yu2, FU Ti-hua1, REN Zheng-long1   

  1. 1. State Key Laboratory of Plant Genetics and Breeding, Sichuan Agricultural University, Yaan 625014, Sichuan, China;
    2. Department of Basic Sciences, Sichuan Agricultural University, Yaan 625014, Sichuan, China
  • Received:2001-09-01 Online:2001-12-31 Published:2017-03-06

摘要: 通过SDS-PAGE、A-PAGE方法对两个小麦-黑麦远缘杂交高代抗病株系98-1104、98-917共26个材料的高分子量谷蛋白亚基的组成、醇溶蛋白Gli-B1l特异位点的有无分别进行了分析。结果表明,在这26个材料的Glu-A1、Glu-B1、Glu-D1位点上分别检测到了2、3、2个等位基因,在每个位点上,出现频率最高的等位基因分别为Glu-A1a(96.15%)、Glu-B1b(92.30%)、Glu-D1d(84.62%)。Nei's遗传变异系数H分析表明:供试材料在Glu-D1位点上变异最大,其次是Glu-B1、Glu-A1;其中株系98-1104在Glu-A1、Glu-B1、Glu-D1位点上的遗传变异系数H分别为0、0.180、0.180,株系98-917在这3个位点上的遗传变异系数H相应为0.117、0.117、0.305。从高分子量谷蛋白亚基组成分析可知,此高代抗病株系高分子量谷蛋白亚基组合方式共有5种:(1、7+8、5+10)、(1、7+9、2+12)、(1、7+8、2+12)、(N、7+8、5+10)、(1、14+15、5+10);其中亲本A42912类型(1、7+8、5+10)所占比例最多,为80.77%。另外通过A-PAGE方法检测出4个具有亚基组成变异的材料98-1104-9(1、7+9、2+12)、98-917-15(1、7+8、2+12)、98-917-27(N、7+8、5+10)、98-917-29(1、14+15、5+10)均为1RS/1BL易。

关键词: Glu-1位点, Gli-B1l位点, 十二烷基磺酸钠聚丙烯酰胺凝胶电泳, 酸性聚丙烯酰胺凝胶电泳, 高分子量谷蛋白亚基, 醇溶蛋白

Abstract: HMW-GS composition at Glu-1 loci was analysed in 26 accessions of two advanced resistant wheat lines derived from wheat rye hybrids by using sodium dodeyl sulfate polyacrylamide gel electrophoresis(SDS-PAGE), Gliadin Gli-B1l loci identified by acid polyacrylamide gel electrophoresis(A-PAGE). From the glutenin patterns, 2, 3, 2 alleles were identified at Glu-A1, Glu-B1 and Glu-D1 loci, respectively in these materials. At each locus, the highest frequency alleles were Glu-A1a(96.15%), Glu-B1b(92.30%) and Glu-D1d(84.62%). The Nei's genetic variation indexes(H) indicate that the highest genetic diversity is found at Glu-D1 loci, the higher is found at Glu-B1 loci, while the lowest is Glu-A1 loci; the H of 98-1104 line at Glu-A1, Glu-B1 and Glu-D1 loci are 0, 0.180, 0.180, correspondingly; for 98-917 line, the H at three loci are 0.117, 0.117, 0.305 correspondingly. Further HMW-GS combination analysis of advanced resistant wheat lines shows there are five types:(1, 7+8, 5+10), (1, 7+9, 2+12), (1, 7+8, 2+12), (N, 7+8, 5+10), (1, 14+15, 5+10); therein the highest frequency composition is the model of Parent A42912(1, 7+8, 5+10). The gliadin patterns indicate that four variable materials at Glu-1 loci:98-1104-9(1, 7+9, 2+12), 98-917-15(1, 7+8, 2+12), 98-917-27(N, 7+8, 5+10), 98-917, 29(1, 14+15, 5+10) are 1RS/1BL translocation lines. Ultimately the mechanism of allele variation of Glu-1 loci1induced by 1RS/1BL translocation is discussed.

Key words: GLU-1 LOCI, GLI-B1L LOCI, SDS-PAGE, A-PAGE, HMW-GS, GLIADIN

中图分类号: 

  • S512.332.2