Seed-storage-protein loci in RFLP maps of diploid, tetraploid, and hexaploid wheat

Linkages between high- and low-molecular-weight (Mr) glutenin, gliadin and triticin loci in diploid, tetraploid and hexaploid wheats were studied by hybridization of restriction fragments with DNA clones and by SDS-PAGE. In tetraploid and hexaploid wheat, DNA fragments hybridizing with a low-Mr glut...

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Veröffentlicht in:Theoretical and applied genetics 1997-11, Vol.95 (7), p.1169-1180
Hauptverfasser: Dubcovsky, J, Echaide, M, Giancola, S, Rousset, M, Luo, M.C, Joppa, L.R, Dvorak, J
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container_end_page 1180
container_issue 7
container_start_page 1169
container_title Theoretical and applied genetics
container_volume 95
creator Dubcovsky, J
Echaide, M
Giancola, S
Rousset, M
Luo, M.C
Joppa, L.R
Dvorak, J
description Linkages between high- and low-molecular-weight (Mr) glutenin, gliadin and triticin loci in diploid, tetraploid and hexaploid wheats were studied by hybridization of restriction fragments with DNA clones and by SDS-PAGE. In tetraploid and hexaploid wheat, DNA fragments hybridizing with a low-Mr glutenin clone were mapped at the XGlu-3 locus in the distal region of the maps of chromosome arms 1AS, 1BS, and 1DS. A second locus, designated XGlu-B2, was detected in the middle of the map of chromosome arm 1BS completely linked to the XGli-B3 gliadin locus. The restriction fragments mapped at this locus were shown to co-segregate with B subunits of low-Mr glutenins in SDS-PAGE in tetraploid wheat, indicating that XGlu-B2 is an active low-Mr glutenin locus. A new locus hybridizing with the low-Mr clone was mapped on the long arm of chromosome 7A(m) in diploid wheat. No glutenin protein was found to co-segregate with this new locus. Triticin loci were mapped on chromosome arms 1AS, 1BS, and 1DS. A failure to detect triticin proteins co-segregating with DNA fragments mapped at XTri-B1 locus suggests that this locus is not active. No evidence was found for the existence of Gli-A4, and it is concluded that this locus is probably synonymous with Gli-A3. Recombination was observed within the multigene gliadin family mapped at XGli-A1 (1.2 cM). Although these closely linked loci may correspond to the previously named Gli-A1 and Gli-A5 loci, they were temporarily designated XGli-A1.1 and XGli-A1.2 until orthology with Gli-A1 and Gli-A5 is established.
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In tetraploid and hexaploid wheat, DNA fragments hybridizing with a low-Mr glutenin clone were mapped at the XGlu-3 locus in the distal region of the maps of chromosome arms 1AS, 1BS, and 1DS. A second locus, designated XGlu-B2, was detected in the middle of the map of chromosome arm 1BS completely linked to the XGli-B3 gliadin locus. The restriction fragments mapped at this locus were shown to co-segregate with B subunits of low-Mr glutenins in SDS-PAGE in tetraploid wheat, indicating that XGlu-B2 is an active low-Mr glutenin locus. A new locus hybridizing with the low-Mr clone was mapped on the long arm of chromosome 7A(m) in diploid wheat. No glutenin protein was found to co-segregate with this new locus. Triticin loci were mapped on chromosome arms 1AS, 1BS, and 1DS. A failure to detect triticin proteins co-segregating with DNA fragments mapped at XTri-B1 locus suggests that this locus is not active. No evidence was found for the existence of Gli-A4, and it is concluded that this locus is probably synonymous with Gli-A3. Recombination was observed within the multigene gliadin family mapped at XGli-A1 (1.2 cM). Although these closely linked loci may correspond to the previously named Gli-A1 and Gli-A5 loci, they were temporarily designated XGli-A1.1 and XGli-A1.2 until orthology with Gli-A1 and Gli-A5 is established.</description><identifier>ISSN: 0040-5752</identifier><identifier>EISSN: 1432-2242</identifier><identifier>DOI: 10.1007/s001220050678</identifier><identifier>CODEN: THAGA6</identifier><language>eng</language><publisher>Heidelberg: Springer</publisher><subject>Biological and medical sciences ; chromosome mapping ; Classical genetics, quantitative genetics, hybrids ; Deoxyribonucleic acid ; DNA ; Fundamental and applied biological sciences. Psychology ; Genetic aspects ; genetic markers ; genetic recombination ; Genetics ; Genetics of eukaryotes. 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No evidence was found for the existence of Gli-A4, and it is concluded that this locus is probably synonymous with Gli-A3. Recombination was observed within the multigene gliadin family mapped at XGli-A1 (1.2 cM). Although these closely linked loci may correspond to the previously named Gli-A1 and Gli-A5 loci, they were temporarily designated XGli-A1.1 and XGli-A1.2 until orthology with Gli-A1 and Gli-A5 is established.</description><subject>Biological and medical sciences</subject><subject>chromosome mapping</subject><subject>Classical genetics, quantitative genetics, hybrids</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Genetic aspects</subject><subject>genetic markers</subject><subject>genetic recombination</subject><subject>Genetics</subject><subject>Genetics of eukaryotes. 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In tetraploid and hexaploid wheat, DNA fragments hybridizing with a low-Mr glutenin clone were mapped at the XGlu-3 locus in the distal region of the maps of chromosome arms 1AS, 1BS, and 1DS. A second locus, designated XGlu-B2, was detected in the middle of the map of chromosome arm 1BS completely linked to the XGli-B3 gliadin locus. The restriction fragments mapped at this locus were shown to co-segregate with B subunits of low-Mr glutenins in SDS-PAGE in tetraploid wheat, indicating that XGlu-B2 is an active low-Mr glutenin locus. A new locus hybridizing with the low-Mr clone was mapped on the long arm of chromosome 7A(m) in diploid wheat. No glutenin protein was found to co-segregate with this new locus. Triticin loci were mapped on chromosome arms 1AS, 1BS, and 1DS. A failure to detect triticin proteins co-segregating with DNA fragments mapped at XTri-B1 locus suggests that this locus is not active. No evidence was found for the existence of Gli-A4, and it is concluded that this locus is probably synonymous with Gli-A3. Recombination was observed within the multigene gliadin family mapped at XGli-A1 (1.2 cM). Although these closely linked loci may correspond to the previously named Gli-A1 and Gli-A5 loci, they were temporarily designated XGli-A1.1 and XGli-A1.2 until orthology with Gli-A1 and Gli-A5 is established.</abstract><cop>Heidelberg</cop><cop>Berlin</cop><pub>Springer</pub><doi>10.1007/s001220050678</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record>
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identifier ISSN: 0040-5752
ispartof Theoretical and applied genetics, 1997-11, Vol.95 (7), p.1169-1180
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language eng
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subjects Biological and medical sciences
chromosome mapping
Classical genetics, quantitative genetics, hybrids
Deoxyribonucleic acid
DNA
Fundamental and applied biological sciences. Psychology
Genetic aspects
genetic markers
genetic recombination
Genetics
Genetics of eukaryotes. Biological and molecular evolution
Genomics
gliadin
glutenins
Life Sciences
linkage (genetics)
loci
multigene family
Physiological aspects
Plant genetics
plant proteins
Polyploidy
Pteridophyta, spermatophyta
Quantitative genetics
restriction fragment length polymorphism
triticin
Triticum aestivum
Triticum monococcum
Triticum turgidum
Vegetals
Wheat
xgli-b3 locus
xglu-3 locus
xglu-b2 locus
xtri-b1 locus
title Seed-storage-protein loci in RFLP maps of diploid, tetraploid, and hexaploid wheat
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