Double dose efficiency of the yellow rust resistance gene Yr17 in bread wheat lines

2019 ◽  
Vol 139 (2) ◽  
pp. 263-271
Author(s):  
Olivier Coriton ◽  
Joseph Jahier ◽  
Marc Leconte ◽  
Virginie Huteau ◽  
Gwenn Trotoux ◽  
...  
2018 ◽  
Vol 55 (1) ◽  
pp. 35-37
Author(s):  
N.N. Vozhzhova ◽  
◽  
N.T. Kupreyshvili ◽  
A.Yu. Myshastaya ◽  
A.A. Yatsyna ◽  
...  

1999 ◽  
Vol 44 (19) ◽  
pp. 1774-1778 ◽  
Author(s):  
Jianxin Ma ◽  
Ronghua Zhou ◽  
Yuchen Dong ◽  
Xiaoming Wang ◽  
Jizeng Jia

2019 ◽  
Author(s):  
Laura-Jayne Gardiner ◽  
Pauline Bansept-Basler ◽  
Mohamed El-Soda ◽  
Anthony Hall ◽  
Donal M. O’Sullivan

AbstractWe 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.HighlightWe show progression from genetic mapping to mapping-by-sequencing and the overlap of defined intervals by each approach culminating with interval refinement and identification of a candidate gene for disease resistance.


PLoS ONE ◽  
2020 ◽  
Vol 15 (4) ◽  
pp. e0231157 ◽  
Author(s):  
Laura-Jayne Gardiner ◽  
Pauline Bansept-Basler ◽  
Mohamed El-Soda ◽  
Anthony Hall ◽  
Donal M. O’Sullivan

Genetics ◽  
2003 ◽  
Vol 164 (2) ◽  
pp. 655-664 ◽  
Author(s):  
Li Huang ◽  
Steven A Brooks ◽  
Wanlong Li ◽  
John P Fellers ◽  
Harold N Trick ◽  
...  

Abstract We report the map-based cloning of the leaf rust resistance gene Lr21, previously mapped to a generich region at the distal end of chromosome arm 1DS of bread wheat (Triticum aestivum L.). Molecular cloning of Lr21 was facilitated by diploid/polyploid shuttle mapping strategy. Cloning of Lr21 was confirmed by genetic transformation and by a stably inherited resistance phenotype in transgenic plants. Lr21 spans 4318 bp and encodes a 1080-amino-acid protein containing a conserved nucleotide-binding site (NBS) domain, 13 imperfect leucine-rich repeats (LRRs), and a unique 151-amino-acid sequence missing from known NBS-LRR proteins at the N terminus. Fine-structure genetic analysis at the Lr21 locus detected a noncrossover (recombination without exchange of flanking markers) within a 1415-bp region resulting from either a gene conversion tract of at least 191 bp or a double crossover. The successful map-based cloning approach as demonstrated here now opens the door for cloning of many crop-specific agronomic traits located in the gene-rich regions of bread wheat.


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