Gupta Sudhir Kumar, Charpe Ashwini, Koul Sunita, Prabhu Kumble Vinod, Haq Qazi Mohd Rizwanul
National Phytotron Facility, Indian Agricultural Research Institute, New Delhi, India.
Genome. 2005 Oct;48(5):823-30. doi: 10.1139/g05-051.
An Aegilops umbellulata-derived leaf-rust-resistance gene, Lr9, was tagged with 3 random amplified polymorphic DNA (RAPD) markers, which mapped within 1.8 cM of gene Lr9 located on chromosome 6BL of wheat. The markers were identified in an F2 population segregating for leaf-rust resistance, which was generated from a cross between 2 near-isogenic lines that differed in the alien gene Lr9 in a widely adopted agronomic background of cultivar 'HD 2329'. Disease phenotyping was done in controlled environmental conditions by inoculating the population with the most virulent pathotype, 121 R63-1 of Puccinia triticina. One RAPD marker, S5550, located at a distance of 0.8+/-0.008 cM from the Lr9 locus, was converted to sequence-characterized amplified region (SCAR) marker SCS5550. The SCAR marker was validated for its specificity to gene Lr9 against 44 of the 50 known Lr genes and 10 wheat cultivars possessing the gene Lr9. Marker SCS5550 was used with another SCAR marker, SCS73719, previously identified as being linked to gene Lr24 on a segregating F2 population to select for genes Lr9 and Lr24, respectively, demonstrating the utility of the 2 markers in marker-assisted gene pyramiding for leaf-rust resistance in wheat.
从小伞山羊草中获得的抗叶锈病基因Lr9,被3个随机扩增多态性DNA(RAPD)标记所标记,这些标记位于小麦6BL染色体上Lr9基因的1.8厘摩范围内。这些标记是在一个对叶锈病抗性进行分离的F2群体中鉴定出来的,该群体是由两个近等基因系杂交产生的,这两个近等基因系在广泛种植的“HD 2329”品种的农艺背景下,在外源基因Lr9上存在差异。通过用小麦叶锈菌最具毒性的致病型121 R63 - 1接种该群体,在可控环境条件下进行病害表型分析。一个位于距Lr9基因座0.8±0.008厘摩处的RAPD标记S5550,被转化为序列特征性扩增区域(SCAR)标记SCS5550。针对50个已知Lr基因中的44个以及10个含有Lr9基因的小麦品种,验证了该SCAR标记对Lr9基因的特异性。标记SCS5550与另一个先前鉴定为与Lr24基因连锁的SCAR标记SCS73719一起,用于在一个分离的F2群体中分别选择Lr9和Lr24基因,证明了这两个标记在小麦抗叶锈病标记辅助基因聚合中的实用性。