首页> 外文期刊>Theoretical and Applied Genetics: International Journal of Breeding Research and Cell Genetics >The complex quantitative barley-Rhynchosporium secalis interaction: newly identified QTL may represent already known resistance genes
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The complex quantitative barley-Rhynchosporium secalis interaction: newly identified QTL may represent already known resistance genes

机译:大麦-Rhynchosporium secalis的复杂定量相互作用:新鉴定的QTL可能代表已知的抗性基因

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Two barley populations, i.e. 135 doubled haploid (DH) lines of the cross 'Igri' (rrs1) x 'Triton' (Rrs1) (I x T) and 76 DH lines of the cross 'Post' x 'Vixen' (both rrs1) (P x V), were analysed to identify QTL for Rhynchosporium secalis resistance independent of the Rrs1 locus by using the single spore R. secalis isolate 271 (Rrs1-virulent). A major QTL with its positive allele derived from cv. 'Triton' was detected in the I x T population on chromosome 2HS explaining almost 80% of the phenotypic variance. Thus, it can be considered as an R-gene corresponding to the already described Rrs15(CI8288) on chromosome 2HS. In addition, two minor QTL were identified, one in the centromeric region of 6H in a highly polymorphic region with already several mapped R-genes and a second one at the end of the short arm of chromosome 7H which may be an allele of Rrs2 because of its chromosomal position. Regarding the DH population P x V different minor QTL were identified on chromosomes 6H and 7H. The first one is corresponding to the genomic region of the Rrs13 gene whereas the QTL on chromosome 7H maps in a genomic region where several R-genes against different pathogens have been localized. A comparison of both QTL analyses reveals no R. secalis isolate 271-specific resistance locus but leads to the hypothesis that two of the identified QTL may be alleles of the R-genes Rrs15(CI8288) and Rrs2.
机译:两个大麦种群,即'Igri'(rrs1)x'Triton'(Rrs1)(I x T)杂交的135双倍单倍体(DH)系和'Post'x'Vixen'杂交的76 DH系(均为rrs1 )(P x V),通过使用单个孢子沙雷氏菌分离株271(Rrs1-毒力)进行分析,以鉴定与Rrs1基因座无关的沙门氏菌的QTL。一个主要的QTL,其阳性等位基因来自cv。在2HS染色体的I x T群体中检测到“ Triton”,这解释了近80%的表型变异。因此,可以认为它是对应于染色体2HS上已经描述的Rrs15(CI8288)的R基因。此外,鉴定出两个较小的QTL,一个位于6H着丝粒区域中的高度多态性区域,该区域已具有多个定位的R基因,另一个位于QH 7H短臂末端,其可能是Rrs2的等位基因,因为的染色体位置。关于DH群体P x V,在6H和7H染色体上鉴定出不同的次要QTL。第一个对应于Rrs13基因的基因组区域,而7H染色体上的QTL位于一个基因组区域,在该基因组区域中已定位了针对不同病原体的几个R基因。两种QTL分析的比较显示没有沙雷氏菌分离株271特异性抗性基因座,但得出这样一个假设,即已鉴定的QTL中的两个可能是R基因Rrs15(CI8288)和Rrs2的等位基因。

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