Abstract

The gene Pm61 that confers powdery mildew resistance has been previously identified on chromosome arm 4AL in Chinese wheat landrace Xuxusanyuehuang (XXSYH). To facilitate the use of Pm61 in breeding practices, the bulked segregant analysis-RNA-Seq (BSR-Seq) analysis, in combination with the information on the Chinese Spring reference genome sequence, was performed in the F2:3 mapping population of XXSYH × Zhongzuo 9504. Two single nucleotide polymorphism (SNP), two Kompetitive Allele Specific PCR (KASP), and six simple sequence repeat (SSR) markers, together with previously identified polymorphic markers, saturated the genetic linkage map for Pm61, especially in the proximal side of the target gene that was short of gene-linked markers. In the newly established genetic linkage map, Pm61 was located in a 0.71 cM genetic interval and can be detected in a high throughput scale by the KASP markers Xicsk8 and Xicsk13 or by the standard PCR-based markers Xicscx497 and Xicsx538. The newly saturated genetic linkage map will be useful in molecular marker assisted-selection of Pm61 in breeding for disease resistant cultivar and in its map-based cloning.

Highlights

  • Powdery mildew is one of the most widely epidemic diseases in wheat (Triticum aestivum L.) grown in the temperate and humid regions of the world

  • The single nucleotide polymorphism (SNP) markers can be visualized by converting them into Kompetitive Allele Specific PCR (KASP) markers for establishing high-throughput genotyping platform for marker-assisted selection (MAS) of the target genes [26]

  • Thirty Blumeria graminis f. sp. tritici (Bgt) isolates collected from wheat fields in Shandong, Shanxi, Beijing, Hebei, and Sichuan provinces were used to test response of XXSYH to powdery mildew

Read more

Summary

Introduction

Powdery mildew is one of the most widely epidemic diseases in wheat (Triticum aestivum L.) grown in the temperate and humid regions of the world. The SNP markers can be visualized by converting them into Kompetitive Allele Specific PCR (KASP) markers for establishing high-throughput genotyping platform for MAS of the target genes [26] They have been used to detect disease resistance genes, such as Sr26 for resistance to stem rust BSR-seq technique, which integrates bulked segregant analysis and RNA-seq [29], has proven to be a rapid and efficient strategy to identify gene-linked molecular markers It provides a fast and high-throughput method to localize resistance genes in crops with large genome, e.g., wheat. Taking the advantage of BSR-seq and the Chinese Spring reference genome sequence, this study was conducted to (1) saturate genetic linkage map for Pm61, and (2) develop PCR-based markers for breeder-friendly use and KASP markers for large scale and high-throughput detection of Pm61 during its MAS

Evaluation of Resistance to Bgt Isolates in XXSYH
Discussion
Plant Materials
Assessments of Resistance to Powdery Mildew
BSR-Seq Analysis
Development and Validation of SNP Markers
Conversion of SNP Markers to KASP Markers
Development of SSR Markers
Construction of High-Density Genetic Linkage Map
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call