Molecular mapping and marker development for the Triticum dicoccoides-derived stripe rust resistance gene YrSM139-1B in bread wheat cv. Shaanmai 139.
Identifieur interne : 000425 ( Main/Corpus ); précédent : 000424; suivant : 000426Molecular mapping and marker development for the Triticum dicoccoides-derived stripe rust resistance gene YrSM139-1B in bread wheat cv. Shaanmai 139.
Auteurs : Hong Zhang ; Lu Zhang ; Changyou Wang ; Yajuan Wang ; Xinli Zhou ; Shikai Lv ; Xinlun Liu ; Zhensheng Kang ; Wanquan JiSource :
- TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik [ 1432-2242 ] ; 2016.
English descriptors
- KwdEn :
- Alleles (MeSH), Basidiomycota (MeSH), Chromosome Mapping (MeSH), DNA, Plant (genetics), Disease Resistance (genetics), Expressed Sequence Tags (MeSH), Genes, Plant (MeSH), Genetic Markers (MeSH), Microsatellite Repeats (MeSH), Plant Diseases (genetics), Plant Diseases (microbiology), Sequence Tagged Sites (MeSH), Triticum (genetics), Triticum (microbiology).
- MESH :
- chemical , genetics : DNA, Plant.
- genetics : Disease Resistance, Plant Diseases, Triticum.
- microbiology : Plant Diseases, Triticum.
- Alleles, Basidiomycota, Chromosome Mapping, Expressed Sequence Tags, Genes, Plant, Genetic Markers, Microsatellite Repeats, Sequence Tagged Sites.
Abstract
KEY MESSAGE
YrSM139-1B maybe a new gene for effective resistance to stripe rust and useful flanking markers for marker-assisted selection were developed.
ABSTRACT
Stripe rust, caused by Puccinia striiformis f. sp. tritici, is an important foliar disease of wheat. Two dominant stripe rust resistant genes YrSM139-1B and YrSM139-2D were pyramided in bread wheat cultivar Shaanmai 139; one from wild emmer and the other from Thinopyrum intermedium. Three near-isogenic F7:8 line pairs (contrasting RILs), N122-1013R/S, N122-185R/S, and N122-1812R/S, independently derived from different F2 plants and differing at the YrSM139-1B locus were generated from the cross Shaanmai 139 × Hu 901-19 through marker-assisted selection. A large F2:3 population from cross N122-1013R × N122-1013S tested for stripe rust response and subjected to analysis with markers in the 1BS10-0.5 bin region using SSR expressed sequence tags (EST) and site-specific sequence markers developed from the 90 K Illumina iSelect SNP array. Five EST-STS markers and four allele-specific PCR markers were mapped to the YrSM139-1B region. The 30.5 cM genetic map for YrSM139-1B consisted of nine markers, two of which were closer to YrSM139-1B than Xgwm273, which was used in producing the contrasting RIL pairs. Race response data and allelism tests showed that YrSM139-1B is different from Yr10, Yr15, and Yr24/26/CH42.
DOI: 10.1007/s00122-015-2633-7
PubMed: 26649867
Links to Exploration step
pubmed:26649867Le document en format XML
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<affiliation><nlm:affiliation>College of Plant Protection, Northwest A&F University, Yangling, 712100, Shaanxi, China. zhangh1129@nwafu.edu.cn.</nlm:affiliation>
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<term>DNA, Plant (genetics)</term>
<term>Disease Resistance (genetics)</term>
<term>Expressed Sequence Tags (MeSH)</term>
<term>Genes, Plant (MeSH)</term>
<term>Genetic Markers (MeSH)</term>
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<term>Plant Diseases (genetics)</term>
<term>Plant Diseases (microbiology)</term>
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<front><div type="abstract" xml:lang="en"><p><b>KEY MESSAGE</b>
</p>
<p>YrSM139-1B maybe a new gene for effective resistance to stripe rust and useful flanking markers for marker-assisted selection were developed.</p>
</div>
<div type="abstract" xml:lang="en"><p><b>ABSTRACT</b>
</p>
<p>Stripe rust, caused by Puccinia striiformis f. sp. tritici, is an important foliar disease of wheat. Two dominant stripe rust resistant genes YrSM139-1B and YrSM139-2D were pyramided in bread wheat cultivar Shaanmai 139; one from wild emmer and the other from Thinopyrum intermedium. Three near-isogenic F7:8 line pairs (contrasting RILs), N122-1013R/S, N122-185R/S, and N122-1812R/S, independently derived from different F2 plants and differing at the YrSM139-1B locus were generated from the cross Shaanmai 139 × Hu 901-19 through marker-assisted selection. A large F2:3 population from cross N122-1013R × N122-1013S tested for stripe rust response and subjected to analysis with markers in the 1BS10-0.5 bin region using SSR expressed sequence tags (EST) and site-specific sequence markers developed from the 90 K Illumina iSelect SNP array. Five EST-STS markers and four allele-specific PCR markers were mapped to the YrSM139-1B region. The 30.5 cM genetic map for YrSM139-1B consisted of nine markers, two of which were closer to YrSM139-1B than Xgwm273, which was used in producing the contrasting RIL pairs. Race response data and allelism tests showed that YrSM139-1B is different from Yr10, Yr15, and Yr24/26/CH42.</p>
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<ArticleTitle>Molecular mapping and marker development for the Triticum dicoccoides-derived stripe rust resistance gene YrSM139-1B in bread wheat cv. Shaanmai 139.</ArticleTitle>
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<Abstract><AbstractText Label="KEY MESSAGE" NlmCategory="CONCLUSIONS">YrSM139-1B maybe a new gene for effective resistance to stripe rust and useful flanking markers for marker-assisted selection were developed.</AbstractText>
<AbstractText Label="ABSTRACT" NlmCategory="UNASSIGNED">Stripe rust, caused by Puccinia striiformis f. sp. tritici, is an important foliar disease of wheat. Two dominant stripe rust resistant genes YrSM139-1B and YrSM139-2D were pyramided in bread wheat cultivar Shaanmai 139; one from wild emmer and the other from Thinopyrum intermedium. Three near-isogenic F7:8 line pairs (contrasting RILs), N122-1013R/S, N122-185R/S, and N122-1812R/S, independently derived from different F2 plants and differing at the YrSM139-1B locus were generated from the cross Shaanmai 139 × Hu 901-19 through marker-assisted selection. A large F2:3 population from cross N122-1013R × N122-1013S tested for stripe rust response and subjected to analysis with markers in the 1BS10-0.5 bin region using SSR expressed sequence tags (EST) and site-specific sequence markers developed from the 90 K Illumina iSelect SNP array. Five EST-STS markers and four allele-specific PCR markers were mapped to the YrSM139-1B region. The 30.5 cM genetic map for YrSM139-1B consisted of nine markers, two of which were closer to YrSM139-1B than Xgwm273, which was used in producing the contrasting RIL pairs. Race response data and allelism tests showed that YrSM139-1B is different from Yr10, Yr15, and Yr24/26/CH42.</AbstractText>
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