Chagué V, Fahima T, Dahan A, Sun G L, Korol A B, Ronin Y I, Grama A, Röder M S, Nevo E
Institute of Evolution, University of Haifa, Mount Carmel, Israel.
Genome. 1999 Dec;42(6):1050-6. doi: 10.1139/g99-064.
Microsatellite and random amplified polymorphic DNA (RAPD) primers were used to identify molecular markers linked to the Yr15 gene which confer resistance to stripe rust (Puccina striiformis Westend) in wheat. By using near isogenic lines (NILs) for the Yr15 gene and a F2 mapping population derived from crosses of these lines and phenotyped for resistance, we identified one microsatellite marker (GWM33) and one RAPD marker (OPA19(800)) linked to Yr15. Then, bulked segregant analysis was used in addition to the NILs to identify RAPD markers linked to the target gene. Using this approach, two RAPD markers linked to Yr15 were identified, one in coupling (UBC199(700)) and one in repulsion phase (UBC212(1200)). After MAPMAKER linkage analysis on the F2 population, the two closest markers were shown to be linked to Yr15 within a distance of about 12 cM. The recombination rates were recalculated using the maximum likelihood technique to take into account putative escaped individuals from the stripe rust resistance test and obtain unbiased distance estimates. As a result of this study, the stripe rust resistance gene Yr15 is surrounded by two flanking PCR markers, UBC199(700) and GWM33, at about 5 cM from each side.
利用微卫星和随机扩增多态性DNA(RAPD)引物来鉴定与小麦抗条锈病(Puccina striiformis Westend)的Yr15基因连锁的分子标记。通过使用Yr15基因的近等基因系(NILs)以及由这些品系杂交产生的F2作图群体,并对其进行抗条锈病表型鉴定,我们鉴定出一个与Yr15连锁的微卫星标记(GWM33)和一个RAPD标记(OPA19(800))。然后,除了NILs之外,还使用混合分组分析法来鉴定与目标基因连锁的RAPD标记。采用这种方法,鉴定出两个与Yr15连锁的RAPD标记,一个处于相引组(UBC199(700)),另一个处于相斥组(UBC212(1200))。对F2群体进行MAPMAKER连锁分析后,显示两个最紧密的标记与Yr15连锁,距离约为12厘摩。使用最大似然技术重新计算重组率,以考虑条锈病抗性测试中可能逃逸的个体,并获得无偏距离估计。本研究结果表明,条锈病抗性基因Yr15两侧各有一个侧翼PCR标记UBC199(700)和GWM33,距离约为5厘摩。