期刊文献+

山羊草Aegilops kotschyi及其供体种Ae.longissima和Ae.umbellulata的醇溶蛋白研究

Gliadin Variations in Aegilops kotschyi and its Progentiors Ae. longissima and Ae. umbellulata
下载PDF
导出
摘要 采用酸性聚丙烯酰胺凝胶电泳(APAGE)法对11份Aegilops kotschyi及其S^1染色体组供体种Ae.longissima2份和U染色体组供体种Ae.umbellulata6份进行了醇溶蛋白位点的研究。结果表明:11份Ae.kotschyi共分离出32条带,31条具有多态性,占96.88%,每份材料可以分离出10~17条谱带,其中仅1条(3.12%)是共有带;11份Ae.kotschyi的遗传距离的变异范围在0~0.704之间,平均为0.409;11份Ae.kotschyi分离出的多数醇溶蛋白谱带均与其染色体组供体种Ae.longissi-ma及Ae.umbellulata相同,但仍有8条谱带未在两供体种中找到;11份Ae.kotschyi的醇溶蛋白多态性(96.88%)明显高于Ae.longissima(52.94%)与Ae.umbellulata(88.89%);11份Ae.kotschyi中有4份表现出了一定的特征带,分析知可能在γ区发生了较大的变异。 Using acid polyacrylamide gel eletrophoresis(APAGE), the gliadin variation of 11 Ae. kotschyi accessions and its progentiors, 2 Ae. longissima accessions and 6 Ae. umbellulata accessions were analyzed. Thirty-two gliadin bands were separated by electrophoresis and thirty-one out of them showed polymorphism (96.88%). Each material had 10 to 17 bands and only 1 band was involved in all of the 11 Ae. kotschyi accessions . The genetic distance (GD) of 11 Ae. kotschyi accessions based on gliadin ranged from 0 to 0. 704, with an average of 0.409. The patterns separated in the 11 Ae. kotschyi accessions were mostly derived from Ae. longissima or Ae. umbellulata , though 8 bands weren't found in the two progentiors. Polymophism of Ae. kotschyi (96.88 % ) was obvious higher than Ae. longissima (52. 94 % ) or Ae. umbellulata (88. 89 % ); 4 out of the 11 Ae. kotschyi accessions had specitie bands. It probably indicated that the r region in Ae. kotschyi had been changed in comparison with that of Ae. longissima or Ae. umbellulata .
出处 《植物遗传资源学报》 CAS CSCD 2003年第1期75-79,共5页 Journal of Plant Genetic Resources
基金 国家自然科学基金(30070462) 四川省青年基金 四川省科技厅应用项目资助
关键词 山羊草 醇溶蛋白 酸性聚丙烯酰胺凝胶电泳法 APAGE 遗传距离 Aegilops kotschyi Ae. longissima Ae. umbellulata Gliadin
  • 相关文献

参考文献12

  • 1徐乃瑜.小麦属和山羊草属细胞质基因组的遗传分化(综述)[J].遗传,1987,9(6):28-32.
  • 2刘登才,魏育明,郑有良.用新隐性ph基因向小麦转移Aegilops variabilis Eig遗传物质[J].四川农业大学学报,1999,17(3):261-267. 被引量:5
  • 3刘登才 杨足君 等.用含臆性ph基因的小麦转移Aegi1ops variabi1is遗传物质获得新种质TKL1.21世纪小麦遗传育种展望[A]..小麦遗传育种国际学术讨论文集[C].北京:中国农业科技出版社,.251~253.
  • 4颜济 杨俊良.小麦一山羊草复合群[A]..小麦族生物系统学(第一卷)[C].北京:中国农业出版社,1999.150-152.
  • 5Sears E. R, The transfer of leaf rust resistance from Aegilops umbellulata to wheat Brookhaven Symp. Biol, 1956, 9:1 - 22.
  • 6Harvey T L, Martin T J, Livers R W. Resistance to biotype C greenbug in synthetic hexaploid wheats derived from Triticum tauschii. J. Econ. Entomol, 1980, 73 : 387-- 389.
  • 7Riley R, Chapman V,Johnson R. Introduction of yellow rust resistance of Aegiiops comosa into wheat by genetically induced homoelogous recombination. Nature, 1968, 216:383--384.
  • 8Friebe B, Tuleen N, et al . Standard karyotype of Triticum longissimum and its cytogenetic relationship with T. aestivum.Genome, 1993, 36:731--742.
  • 9Friebe B, J Jiang,et al. Standard karyotype of Triticum umbellulatum and the characterization of derived chromosome addition and translocation lines in common wheat. Theor Appl Genet,1995, 90:150-- 156.
  • 10Cooke R J. The classification of wheat cultivars using a standard reference electrophoresis method. J Nat Agric Bor. 1987, 17:273-281.

二级参考文献11

  • 1李合智 庄巧生 等.抗条锈、白粉病种质的评价与利用.中国小麦育种研究进展[M].北京:农业出版社,1996.254-259.
  • 2崔运兴 马缘生.中国特有小麦资源主要遗传性状评价与利用[J].核农学报,1988,2(3):129-138.
  • 3罗明诚 任正隆 等.中国普通小麦地方品种与黑麦杂种F1的细胞遗传学研究.作物育种探索[M].成都:四川科学技术出版社,1992.169-176.
  • 4付体华 任正隆 等.四川小麦自然群体中的ph隐性基因和远缘杂种后代染色体数的两极分化.作物育种探索[M].成都:四川科学技术出版社,1992.177-181.
  • 5杨足君.几个外源物种抗条锈病抗白粉病基因在小麦背景中的表达.四川农业大学博士论文[M].雅安,1999.47-49.
  • 6叶兴国 樊路 等.小麦ph1b、ph2a、ph2b突变体与粘果山羊草杂种及其衍生后代细胞遗传学研究.第二届全国青年作物遗传育种学术讨论[M].北京,1991.88-92.
  • 7余懋群.ph1b基因对普通小麦×Aegilops variabilis杂种F1、BC1、BC2、BC3及转移Meloidogyne naasi基因影响的研究.西南地区遗传学研究[M].成都:四川大学出版社,1996.174.
  • 8杨武云.节节麦基因导入六倍体小麦及其遗传表达中的研究.四川农业大学博士论文[M].雅安,1999.29-41.
  • 9刘登才,罗明诚,杨俊良,颜济,兰秀锦,杨武云.小麦自然群体中部分同源染色体配对促进基因的染色体定位[J].西南农业学报,1997,10(3):10-15. 被引量:4
  • 10马瑞,郑殿升,樊路.普通小麦品种中Ph基因突变体自然存在的可能性研究[J].作物学报,1999,25(1):99-104. 被引量:6

共引文献4

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