Unknown

Dataset Information

0

A framework for gene mapping in wheat demonstrated using the Yr7 yellow rust resistance gene.


ABSTRACT: We used three approaches to map the yellow rust resistance gene Yr7 and identify associated SNPs in wheat. First, we used a traditional QTL mapping approach using a double haploid (DH) population and mapped Yr7 to a low-recombination region of chromosome 2B. To fine map the QTL, we then used an association mapping panel. Both populations were SNP array genotyped allowing alignment of QTL and genome-wide association scans based on common segregating SNPs. Analysis of the association panel spanning the QTL interval, narrowed the interval down to a single haplotype block. Finally, we used mapping-by-sequencing of resistant and susceptible DH bulks to identify a candidate gene in the interval showing high homology to a previously suggested Yr7 candidate and to populate the Yr7 interval with a higher density of polymorphisms. We highlight the power of combining mapping-by-sequencing, delivering a complete list of gene-based segregating polymorphisms in the interval with the high recombination, low LD precision of the association mapping panel. Our mapping-by-sequencing methodology is applicable to any trait and our results validate the approach in wheat, where with a near complete reference genome sequence, we are able to define a small interval containing the causative gene.

SUBMITTER: Gardiner LJ 

PROVIDER: S-EPMC7159211 | biostudies-literature | 2020

REPOSITORIES: biostudies-literature

altmetric image

Publications

A framework for gene mapping in wheat demonstrated using the Yr7 yellow rust resistance gene.

Gardiner Laura-Jayne LJ   Bansept-Basler Pauline P   El-Soda Mohamed M   Hall Anthony A   O'Sullivan Donal M DM  

PloS one 20200415 4


We used three approaches to map the yellow rust resistance gene Yr7 and identify associated SNPs in wheat. First, we used a traditional QTL mapping approach using a double haploid (DH) population and mapped Yr7 to a low-recombination region of chromosome 2B. To fine map the QTL, we then used an association mapping panel. Both populations were SNP array genotyped allowing alignment of QTL and genome-wide association scans based on common segregating SNPs. Analysis of the association panel spannin  ...[more]

Similar Datasets

| PRJEB36010 | ENA
| S-EPMC6567072 | biostudies-literature
| S-EPMC5441593 | biostudies-literature
| S-EPMC8555631 | biostudies-literature
| S-EPMC5026171 | biostudies-literature
| S-EPMC4870046 | biostudies-literature
| S-EPMC9911047 | biostudies-literature
| S-EPMC10140103 | biostudies-literature
| S-EPMC7773921 | biostudies-literature
| S-EPMC7746701 | biostudies-literature