Application of marker-assisted selection and genome-wide association scanning to the development of winter food barley germplasm resources

被引:13
作者
Chutimanitsakun, Yada [1 ]
Cuesta-Marcos, Alfonso [1 ]
Chao, Shiaoman [2 ]
Corey, Ann [1 ]
Filichkin, Tanya [1 ]
Fisk, Scott [1 ]
Kolding, Mathias [3 ]
Meints, Brigid [1 ]
Ong, Yee-Ling [1 ]
Rey, Juan Ignacio [4 ]
Ross, Andrew S. [1 ]
Hayes, Patrick M. [1 ]
机构
[1] Oregon State Univ, Dept Crop & Soil Sci, Corvallis, OR 97331 USA
[2] USDA ARS, Biosci Res Lab, Fargo, ND 58105 USA
[3] Oregon State Univ, Hermiston Agr Res & Extens Serv, Hermiston, OR 97801 USA
[4] Dow Agrosci, Midwest Res Ctr, Fowler, IN 47944 USA
基金
美国食品与农业研究所;
关键词
food barley; low temperature tolerance; marker assisted selection; betaglucan; vernalization; winter barley; LOW-TEMPERATURE TOLERANCE; BETA-GLUCAN CONTENT; POPULATION-STRUCTURE; PHOTOPERIOD RESPONSE; VERNALIZATION1; GENE; SPRING BARLEY; WHEAT; GENOTYPE; STARCH; EXPRESSION;
D O I
10.1111/pbr.12086
中图分类号
S3 [农学(农艺学)];
学科分类号
0901 ;
摘要
Barley (Hordeum vulgare) is an important component of heart-healthy whole grain diets because it contains -glucan. All current US barley varieties with high -glucan are spring habit and have waxy starch. Winter varieties have agronomic advantages but require low-temperature tolerance (LTT). Vernalization sensitivity (VS) is associated with higher levels of LTT. To rapidly develop fall-sown varieties with LTT and higher grain -glucan, we therefore used marker-assisted selection (MAS) at the WX and VRN-H2 loci. The MAS-derived lines, together with unrelated non-waxy germplasm developed via phenotypic selection (PS), were used for a genome-wide association scan (GWAS). The panel was phenotyped for grain -glucan, LTT and VS. It was genotyped with 3072 single-nucleotide polymorphisms (SNPs) and allele-specific primers. Marker-assisted selection fixed target alleles at both loci but only one of the target phenotypes (higher -glucan percentage) was achieved. Variation for VS and LTT is attributable to (i) incomplete information about VRN-H1 at the outset of the project and (ii) unexpected allelic variation at VRN-H3 with a large effect on VS and LTT.
引用
收藏
页码:563 / 570
页数:8
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