A genetic linkage map of Triticum tauschii (DD) and its relationship to the D genome of bread wheat (AABBDD)

Genome ◽  
1991 ◽  
Vol 34 (3) ◽  
pp. 362-374 ◽  
Author(s):  
K. S. Gill ◽  
E. L. Lubbers ◽  
B. S. Gill ◽  
W. J. Raupp ◽  
T. S. Cox

One hundred and seventy-eight loci have been mapped in Triticum tauschii (Coss.) Schmal. (2n = 14, DD) and Triticum aestivum L. em. Thell. (2n = 42, AABBDD). Thirty-five loci were mapped by aneuploid analysis in T. aestivum. One hundred and fifty-two loci, including 143 restriction fragment length polymorphisms (RFLPs), 8 proteins, and 1 leaf rust resistance gene, were mapped in an F2 population (60 plants) of T. tauschii. One hundred and twenty-seven loci were placed in linkage groups belonging to seven D-genome chromosomes of T. tauschii. The source of the probes was a PstI genomic library of T. tauschii, which gave 13% single-low copy clones. Four restriction endonucleases (DraI, EcoRI, EcoRV, HindIII) gave 75% polymorphism between the two parents. Nineteen clones detected multiloci ranging from two to nine in number. Deletions–insertions and point mutations were equally important for generating RFLPs. A hypervariable sequence was identified, which may have potential use in varietal fingerprinting. One marker was found to be linked to a rust-resistance gene. The map will be useful for determining genetic relationships in the Triticeae and for tagging genes of economic importance.Key words: restriction fragment length polymorphism, Triticum aestivum, leaf rust, isozymes, Aegilops squarrosa.

1998 ◽  
Vol 11 (3) ◽  
pp. 242-245 ◽  
Author(s):  
Donna E. Delaney ◽  
Craig A. Webb ◽  
Scot H. Hulbert

The Rp8 rust resistance locus of maize is unique in that only Rp8-A/Rp8-B heterozygotes provide resistance and homozygotes are susceptible. A third allele, Rp8-C, provides no resistance in homozygotes or heterozygous combinations. Rp8 maps to the long arm of chromosome 6, near the restriction fragment length polymorphism marker umc21.


2007 ◽  
Vol 65 (1-2) ◽  
pp. 93-106 ◽  
Author(s):  
Sylvie Cloutier ◽  
Brent D. McCallum ◽  
Caroline Loutre ◽  
Travis W. Banks ◽  
Thomas Wicker ◽  
...  

Genome ◽  
1989 ◽  
Vol 32 (4) ◽  
pp. 724-732 ◽  
Author(s):  
L. N. W. Kam-Morgan ◽  
B. S. Gill ◽  
S. Muthukrishnan

The use of restriction fragment length polymorphisms (RFLPs) as genetic markers in bread wheat, Triticum aestivum, and a wild wheat progenitor, Aegilops squarrosa, was investigated. The objectives were (i) to identify RFLP loci; (ii) to assign cDNA sequences onto specific chromosomes and chromosome arms; and (iii) to determine linkage relationships between RFLP loci. A low level of polymorphism was found, utilizing barley cDNA clones as probes, in hexaploid cultivated wheats. However, accessions of A. squarrosa revealed greater polymorphism. Wheat–barley alien addition lines were used to assign 17 cDNA sequences to specific chromosome groups and ditelosomic and nullisomic–tetrasomic wheat stocks were used to assign these sequences to specific chromosome arms. Of 16 sets of RFLP loci, excluding α-Amy-1 and α-Amy-2, 14 are new sets of loci marking 6 of the 7 homoeologous groups of wheat. The construction of a linkage map of chromosome 5D was initiated by analyzing a segregating F2 population between two homozygous accessions of A. squarrosa. A strategy using wheat aneuploids for chromosome arm location and a segregating A. squarrosa population for linkage measurement was demonstrated for mapping the D-genome chromosomes of wheat.Key words: genetic map, restriction fragment length polymorphisms, Triticum aestivum, Aegilops squarrosa, polyploidy.


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.


2017 ◽  
Vol 67 (2) ◽  
pp. 129-134 ◽  
Author(s):  
Ali Aliakbari Sadeghabad ◽  
Ali Dadkhodaie ◽  
Bahram Heidari ◽  
Hooman Razi ◽  
Reza Mostowfizadeh-Ghalamfarsa

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