The University of Queensland, School of Agriculture and Food Sciences, Brisbane, QLD, 4072, Australia.
Theor Appl Genet. 2011 Jun;123(1):55-68. doi: 10.1007/s00122-011-1566-z. Epub 2011 Mar 15.
A doubled haploid (DH) barley (Hordeum vulgare L.) population of 334 lines (ND24260 × Flagship) genotyped with DArT markers was used to map genes for adult plant resistance (APR) to leaf rust (Puccinia hordei Otth) under field conditions in Australia and Uruguay. The Australian barley cultivar Flagship carries an APR gene (qRphFlag) derived from the cultivar Vada. Association analysis and composite interval mapping identified two genes conferring APR in this DH population. qRphFlag was mapped to the short arm of chromosome 5H (5HS), accounting for 64-85% of the phenotypic variation across four field environments and 56% under controlled environmental conditions (CEC). A second quantitative trait locus (QTL) from ND24260 (qRphND) with smaller effect was mapped to chromosome 6HL. In the absence of qRphFlag, qRphND conferred only a low level of resistance. DH lines displaying the highest level of APR carried both genes. Sequence information for the critical DArT marker bPb-0837 (positioned at 21.2 cM on chromosome 5HS) was used to develop bPb-0837-PCR, a simple PCR-based marker for qRphFlag. The 245 bp fragment for bPb-0837-PCR was detected in a range of barley cultivars known to possess APR, which was consistent with previous tests of allelism, demonstrating that the qRphFlag resistant allele is common in leaf rust resistant cultivars derived from Vada and Emir. qRphFlag has been designated Rph20, the first gene conferring APR to P. hordei to be characterised in barley. The PCR marker will likely be effective in marker-assisted selection for Rph20.
一个由 334 个系(ND24260×Flagship)组成的双单倍体(DH)大麦(Hordeum vulgare L.)群体,利用 DArT 标记进行了基因型分析,用于在澳大利亚和乌拉圭田间条件下对叶锈病(Puccinia hordei Otth)进行成株期抗性(APR)基因定位。澳大利亚大麦品种 Flagship 携带一个 APR 基因(qRphFlag),源自品种 Vada。关联分析和复合区间作图在这个 DH 群体中鉴定出两个赋予 APR 的基因。qRphFlag 被定位到 5HS 染色体的短臂上,占四个田间环境中表型变异的 64-85%,在受控环境条件(CEC)下占 56%。来自 ND24260 的第二个数量性状位点(QTL)qRphND 效应较小,被定位到 6HL 染色体上。在没有 qRphFlag 的情况下,qRphND 只赋予较低水平的抗性。表现出最高 APR 水平的 DH 系携带这两个基因。用于开发 qRphFlag 的关键 DArT 标记 bPb-0837 的序列信息(位于 5HS 染色体上 21.2 cM 处)被用于开发 bPb-0837-PCR,这是一种用于 qRphFlag 的简单基于 PCR 的标记。bPb-0837-PCR 的 245 bp 片段在一系列已知具有 APR 的大麦品种中被检测到,这与等位基因测试的结果一致,证明 qRphFlag 抗性等位基因在源自 Vada 和 Emir 的叶锈病抗性品种中很常见。qRphFlag 被命名为 Rph20,是第一个在大麦中被鉴定的赋予 P. hordei APR 的基因。PCR 标记可能在 Rph20 的标记辅助选择中有效。