Using Next Generation Sequencing for Multiplexed Trait-Linked Markers in Wheat

被引:26
作者
Bernardo, Amy [1 ]
Wang, Shan [2 ]
St Amand, Paul [3 ]
Bai, Guihua [2 ,3 ]
机构
[1] Kansas State Univ, Dept Plant Pathol, Manhattan, KS 66506 USA
[2] Kansas State Univ, Dept Agron, Manhattan, KS 66506 USA
[3] ARS, USDA, Hard Winter Wheat Genet Res Unit, Manhattan, KS USA
基金
美国食品与农业研究所;
关键词
SINGLE NUCLEOTIDE POLYMORPHISM; RUST RESISTANCE GENES; MOLECULAR MARKERS; HEXAPLOID WHEAT; IDENTIFICATION; VALIDATION; CLONING; PCR; GBS;
D O I
10.1371/journal.pone.0143890
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
With the advent of next generation sequencing (NGS) technologies, single nucleotide polymorphisms (SNPs) have become the major type of marker for genotyping in many crops. However, the availability of SNP markers for important traits of bread wheat (Triticum aestivum L.) that can be effectively used in marker-assisted selection (MAS) is still limited and SNP assays for MAS are usually uniplex. A shift from uniplex to multiplex assays will allow the simultaneous analysis of multiple markers and increase MAS efficiency. We designed 33 locus-specific markers from SNP or indel-based marker sequences that linked to 20 different quantitative trait loci (QTL) or genes of agronomic importance in wheat and analyzed the amplicon sequences using an Ion Torrent Proton Sequencer and a custom allele detection pipeline to determine the genotypes of 24 selected germplasm accessions. Among the 33 markers, 27 were successfully multiplexed and 23 had 100% SNP call rates. Results from analysis of "kompetitive allele-specific PCR" (KASP) and sequence tagged site (STS) markers developed from the same loci fully verified the genotype calls of 23 markers. The NGS-based multiplexed assay developed in this study is suitable for rapid and high-throughput screening of SNPs and some indel-based markers in wheat.
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页数:18
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