期刊文献+

应用PCR技术研究四川小麦品种特异性位点遗传多样性

Genetic Diversity among Sichuan Wheat Cultivars Based on STS-PCR Markers
在线阅读 下载PDF
导出
摘要 采用PCR技术对四川省近50年来年推广面积达66700hm2(100万亩)以上的40个小麦品种特异性位点(即STS-PCR标记)的遗传多样性进行了研究。13对STS-PCR引物和26种引物-酶组合中,92 3%的引物和88 5%引物-酶组合能揭示小麦品种间的多态性。在检测到的92条DNA片段中,86 96%具有多态性,平均每种引物-酶组合检测到3 08条(变幅为1~8条)。这些品种间遗传相似系数(GS)变幅为0 478~0 989,平均GS值为0 753。STS-PCR标记遗传距离聚类分析能将40个品种相互区分开,其结果与亲缘关系较一致。各年代品种间GS值变化趋势表明,从60年代后四川小麦品种的遗传多样性呈明显的下降趋势。 The genetic diversity among 40 Sichuan wheat (Tritcum aestivum L) cultivars, which has been popularized above 667×104?hm2 per year in Sichuan Province during recent 50 years, was investigated by using 26 primerenzyme combinations of 13 sequencetaggedsite (STSPCR) primer sets. 12 of 13 primer sets (923%) and 23 of 26 primerenzyme combinations (885%) reveal polymorphisms. A total of 92 restriction fragments has been detected in these cultivars, with 308 fragments per primerenzyme combination. The genetic similarity varies from 0478 to 0989 among 40 genotypes, with the mean of 0753. The results show that 40 genotypes can be distinguished by STSPCR markers. The variation of GS in 5 eras reveals that the genetic similarity has the tendency to increase since 1960.
出处 《四川农业大学学报》 CSCD 2002年第4期309-312,320,共5页 Journal of Sichuan Agricultural University
基金 国家教育部重点项目(00225) 四川省教育厅预研项目(2000-C02) 四川省科技厅农业生物技术专项基金资助。
关键词 PCR技术 品种 特异性位点 遗传多样性 四川 小麦 SICHUAN WHEAT STS-PCR GENETIC SIMILARITY CHUSTER ANALYSIS.
  • 相关文献

参考文献22

  • 1Olson M, Hood L, Canter C, et al. A common language for physical mapping of the human genome[J]. Science, 1989, 254: 1434-1435.
  • 2D'Ovidio, Tanzarella O A, Porceddu E. Rapid and efficient detection of genetic polymorphism in wheat through amplification by polimerase chain reaction[J]. Plant Mol Biol, 1990, 15: 169-171.
  • 3Weining S, P Langridge. Identification and mapping of polymorpgisms in cereals based on the polymerase chain reaction[J]. Theor Appl Genet, 1991, 82: 209-216.
  • 4Talbert L E, Blake N K, Chee P W, et al. Evaluation of "sequence-tagged-site" PCR products as molecular markers in wheat[J]. Theor Appl Genet, 1994, 87: 789-794.
  • 5Chen H B, Martin J M, Lavin M, et al. Genetic diversity in hard spring wheat based on sequence-tagged-site PCR markers[J]. Crop Sci, 1994, 34: 1628-1632.
  • 6Martin J M, Talbert L E, Lanning S P, et al. Hybrid performance in wheat as related to parental diversity[J]. Crop Sci, 1995, 35: 104-108.
  • 7Tragoonrung S, Kanazin V, Hayes P M, et al. Sequence-tagged-site-facilitated PCR for barley genome mapping[J]. Theor Appl Genet, 1992, 84: 1002-1008.
  • 8Komatsuda T, Nakamura I, Takaiwa F, et al. Development of STS markers closely linked to the vrs1 locus in barley, Hordeum vulgare[J]. Genome, 1998, 41: 680-685.
  • 9Roy J K, Prasad M, Varshney R K, et al. Identification of a microsatellite on chromosome 6B and a STS on 7D of bread wheat showing an association with preharvest sprouting tolerance[J]. Theor Appl Genet, 1999, 99: 336-341.
  • 10余遥.四川小麦[M].成都:四川科学技术出版社,1998.271-274.

二级参考文献16

共引文献148

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