The University of Sydney Plant Breeding Institute, School of Life and Environmental Sciences, 107 Cobbitty Road, Cobbitty, NSW, 2570, Australia.
ICAR-Indian Agricultural Research Institute Regional Station, Wellington, India.
Theor Appl Genet. 2018 May;131(5):1091-1098. doi: 10.1007/s00122-018-3060-3. Epub 2018 Feb 2.
A new leaf rust resistance gene Lr79 has been mapped in the long arm of chromosome 3B and a linked marker was identified for marker-assisted selection. Aus26582, a durum wheat landrace from the A. E. Watkins Collection, showed seedling resistance against durum-specific and common wheat-specific Puccinia triticina (Pt) pathotypes. Genetic analysis using a recombinant inbred line (RIL) population developed from a cross between Aus26582 and the susceptible parent Bansi with Australian Pt pathotype showed digenic inheritance and the underlying loci were temporarily named LrAW2 and LrAW3. LrAW2 was located in chromosome 6BS and this study focused on characterisation of LrAW3 using RILs lacking LrAW2. LrAW3 was incorporated into the DArTseq map of Aus26582/Bansi and was located in chromosome 3BL. Markers linked with LrAW3 were developed from the chromosome survey sequence contig 3B_10474240 in which closely-linked DArTseq markers 1128708 and 3948563 were located. Although bulk segregant analysis (BSA) with the 90 K Infinium array identified 51 SNPs associated with LrAW3, only one SNP-derived KASP marker mapped close to the locus. Deletion bin mapping of LrAW3-linked markers located LrAW3 between bins 3BL11-0.85-0.90 and 3BL7-0.63. Since no other all stage leaf rust resistance gene is located in chromosome 3BL, LrAW3 represented a new locus and was designated Lr79. Marker sun786 mapped 1.8 cM distal to Lr79 and Aus26582 was null for this locus. However, the marker can be reliably scored as it also amplifies a monomorphic fragment that serves as an internal control to differentiate the null status of Aus26582 from reaction failure. This marker was validated among a set of durum and common wheat cultivars and was shown to be useful for marker-assisted selection of Lr79 at both ploidy levels.
一个新的叶锈病抗性基因 Lr79 已被定位在 3B 染色体的长臂上,并鉴定出一个与该基因连锁的标记,用于标记辅助选择。Aus26582 是来自 A. E. Watkins 收藏的硬粒小麦地方品种,对硬粒小麦特异性和普通小麦特异性 Puccinia triticina (Pt) 生理小种表现出幼苗抗性。利用 Aus26582 和易感亲本 Bansi 杂交产生的重组自交系(RIL)群体进行的遗传分析表明,该基因具有双基因遗传,其潜在基因暂时命名为 LrAW2 和 LrAW3。LrAW2 位于 6BS 染色体上,本研究重点研究了 RIL 缺乏 LrAW2 时 LrAW3 的特征。LrAW3 被整合到 Aus26582/Bansi 的 DArTseq 图谱中,位于 3BL 染色体上。与 LrAW3 连锁的标记是从染色体调查序列 contig 3B_10474240 中开发的,其中紧密连锁的 DArTseq 标记 1128708 和 3948563 位于该序列中。虽然利用 90 K Infinium 阵列的批量分离分析(BSA)鉴定出与 LrAW3 相关的 51 个 SNP,但只有一个 SNP 衍生的 KASP 标记与该基因座接近。LrAW3 连锁标记的删除 bin 作图将 LrAW3 定位在 3BL11-0.85-0.90 和 3BL7-0.63 两个 bin 之间。由于没有其他所有阶段叶锈病抗性基因位于 3BL 染色体上,因此 LrAW3 代表一个新的基因座,并被命名为 Lr79。标记 sun786 位于 Lr79 远端 1.8 cM 处,Aus26582 在此基因座上为缺失型。然而,该标记可以可靠地进行评分,因为它还扩增了一个单态片段,作为内部对照,可将 Aus26582 的缺失状态与反应失败区分开来。该标记在一组硬粒小麦和普通小麦品种中进行了验证,证明在两种倍性水平下对 Lr79 的标记辅助选择都很有用。