Development of a co-dominant DNA marker tightly linked to gene tardus conferring reduced pod shattering in narrow-leafed lupin (Lupinus angustifolius L.)

被引:22
作者
Li, Xin [1 ,2 ]
Renshaw, Daniel [3 ]
Yang, Huaan [3 ]
Yan, Guijun [1 ,2 ]
机构
[1] Univ Western Australia, Fac Nat & Agr Sci, Sch Plant Biol, Crawley, WA 6009, Australia
[2] Univ Western Australia, Inst Agr, Crawley, WA 6009, Australia
[3] Dept Agr & Food Western Australia, S Perth, WA 6151, Australia
关键词
Marker-assisted selection (MAS); Lupinus angustifolius L; Sequence-specific marker; MFLP; MOLECULAR MARKERS; ANTHRACNOSE DISEASE; PCR MARKERS; SEQUENCE; RESISTANCE; MAP; LEGUME;
D O I
10.1007/s10681-010-0212-1
中图分类号
S3 [农学(农艺学)];
学科分类号
0901 ;
摘要
The reduced pod shattering gene tardus is one of the most important domestication genes in narrow-leafed lupin (Lupinus angustifolius L.). In development of a molecular marker linked to the tardus gene, we incorporated the concept of marker validation during the initial candidate marker identification stage. Four dominant microsatellite-anchored fragment length polymorphism (MFLP) markers were identified as candidate markers based on their banding patterns in an F-8 recombination inbred line (RIL) population. One specific marker best correlating with phenotypes in the representative germplasm was selected and converted to a simple PCR-based marker. This established marker, designated as "TaLi", is located at a distance of 1.4 cM from the tardus gene. DNA sequencing revealed six insertion/deletion sites between the non-shattering marker allele and the shattering marker allele. Validation of marker TaLi on 25 domesticated commercial cultivars and 125 accessions of the lupin core collection found a 94% marker and tardus phenotype match. Marker TaLi is the first simple PCR-based marker that can be widely used for non-shattering pod selection in narrow-leafed lupin breeding program.
引用
收藏
页码:49 / 58
页数:10
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