Identification of a gene for resistance to wheatgrass powdery mildew fungus in the common wheat cultivar Chinese Spring

Genome ◽  
1988 ◽  
Vol 30 (4) ◽  
pp. 612-614 ◽  
Author(s):  
Y. Tosa ◽  
H. Tokunaga ◽  
H. Ogura

A gene for resistance to Erysiphe graminis was detected in Triticum aestivum cv. Chinese Spring, strain Salmon, T. compactum cv. No. 44, and T. spelta var. duhamelianum, using a hybrid culture derived from E. graminis f. sp. agropyri × E. graminis f. sp. tritici. The gene was located on the short arm of chromosome 6B and designated Pm11. Pm11 was considered to be involved in the resistance of wheat to the wheatgrass powdery mildew fungus.Key words: wheat, resistance, powdery mildew, Erysiphe graminis.

Genome ◽  
1987 ◽  
Vol 29 (6) ◽  
pp. 850-852 ◽  
Author(s):  
Y. Tosa ◽  
H. Tsujimoto ◽  
H. Ogura

A gene for resistance to Erysiphe graminis was detected in the common wheat cultivars 'Norin 4', 'Norin 26', 'Norin 29', 'Shin-chunaga', and 'Penjamo 62', using a hybrid culture derived from E. graminis f.sp. agropyri × E. graminis f.sp. tritici. The gene was located on chromosome 1D and designated Pm10. Pm10 was considered to be involved in the resistance of wheat to the wheatgrass powdery mildew fungus. Key words: wheat, resistance, powdery mildew, Erysiphe graminis.


Genome ◽  
1990 ◽  
Vol 33 (2) ◽  
pp. 231-234 ◽  
Author(s):  
Y. Tosa ◽  
S. Tada

The common wheat cultivar 'Chancellor' and its near-isogenic lines carrying resistance genes to Erysiphe graminis f.sp. tritici were inoculated with 240 F1 cultures derived from a cross between E. graminis f.sp. agropyri, Ak-1, and E. graminis f.sp. tritici, Tk-1. Segregation patterns of avirulent and virulent cultures suggested that the F1 population carries avirulence genes corresponding to Pm1, Pm2, Pm3a, and Pm3b. These avirulence genes were considered to be derived from Ak-1. It was therefore concluded that Pm1, Pm2, Pm3a, and Pm3b, resistance genes to E. graminis f.sp. tritici, operate against E. graminis f.sp. agropyri.Key words: powdery mildew, Erysiphe graminis, resistance, wheat, wheatgrass.


Genome ◽  
1989 ◽  
Vol 32 (5) ◽  
pp. 913-917 ◽  
Author(s):  
Y. Tosa

F1 hybrid cultures between Erysiphe graminis f.sp. agropyri (wheatgrass mildew fungus) and E. graminis f.sp. tritici (wheat mildew fungus) were produced by using a common host of the two formae spéciales. When three common wheat cultivars, Triticum aestivum cv. Norin 4, T. aestivum cv. Norin 10, and T. compactum cv. No. 44, were inoculated with a population of F1 cultures, avirulent and virulent cultures segregated in a 3:1 ratio. This indicated that two major genes are involved in the avirulence of E. graminis f.sp. agropyri, Ak-1, on each of the three cultivars. Further analyses revealed that the three pairs of avirulence genes have one gene in common. On T. aestivum cv. Shin-chunaga, T. aestivum cv. Norin 26, and a strain of T. macha, the F1 population segregated in the same pattern as on T. aestivum cv. Norin 4, indicating that the same pair of avirulence genes is operating on these four cultivars. On T. aestivum cv. Red Egyptian the distribution of F1 phenotypes was continuous, suggesting that no major genes are involved in the avirulence of Ak-1 on this cultivar.Key words: powdery mildew, Erysiphe graminis, avirulence, wheat, wheatgrass.


Genome ◽  
2000 ◽  
Vol 43 (2) ◽  
pp. 298-305 ◽  
Author(s):  
Xiuqiang Huang ◽  
Friedrich J Zeller ◽  
Sai LK Hsam ◽  
Gerhard Wenzel ◽  
Volker Mohler

Amplified fragment length polymorphism (AFLP) markers with a total of 256 EcoRI + ANN- MseI + CNN primer combinations were investigated employing the common wheat cultivar Triticum aestivum 'Chinese Spring.' On average, 103 fragments per primer combination were amplified, ranging from a maximum of 226 fragments to a minimum of 18 fragments. The primer combinations E + AAA - M + CNN and E + ATT - M + CNN produced very few distinct fragments. By using 15 randomly chosen EcoRI + ANN - MseI + CNN primer combinations, 928 AFLP markers were allocated to wheat chromosomes, of which 131 were assigned to specific chromosome arms. These AFLP markers were locus-specific and randomly distributed on the different chromosomes. In addition, 6 and 41 AFLP markers were simultaneously absent in two nulli-tetrasomics (NTs) of both homoeologous and non-homoeologous groups, respectively, whereas additional fragments were detected in N1BT1A, N5AT5D, and N6BT6A lines.Key words: aneuploid, chromosome assignment, Triticum aestivum.


2012 ◽  
Vol 48 (8) ◽  
pp. 785-791 ◽  
Author(s):  
V. S. Arbuzova ◽  
E. D. Badaeva ◽  
T. T. Efremova ◽  
T. S. Osadchaya ◽  
N. V. Trubacheeva ◽  
...  

2019 ◽  
Vol 24 ◽  
pp. 109-114 ◽  
Author(s):  
N. A. Kozub ◽  
I. A. Sozinov ◽  
H. Ya. Bidnyk ◽  
N. A. Demianova ◽  
O. I. Sozinova ◽  
...  

Aim. The aim of this study was to isolate and propagate mutants at gliadin loci developed on the basis of the common wheat cultivar Bezostaya 1. Methods. We searched for spontaneous and gamma-irradiation induced mutations at gliadin loci among the progeny of F1 and F2 plants from crosses between near-isogenic lines by gliadin loci on the basis of the cultivar Bezostaya 1, including lines with the wheat-rye 1BL.1RS translocation. To identify mutations, we performed acid polyacrylamide gel electrophoresis and SDS-electrophoresis of storage proteins. Results. On the basis of the common wheat cultivar Bezostaya 1, five mutants (six mutations) at gliadin loci were isolated and propagated, four of which were described for the first time. Three mutations occurred at the Gli-R1 locus involved in the wheat-rye 1BL.1RS translocation (the loss of secalins, intensification of a secalin component, and increased mobility of a secalin component). Two mutations were identified in the allele Gli-B1b, one caused the null-allele at the Gli-A2 locus. Conclusions. The material of mutants is of importance for studying the role of certain groups of storage proteins and their components in quality determination, as well as mechanisms of regulation of storage protein synthesis. Keywords: Triticum aestivum, gliadin, secalin, mutation, 1BL.1RS translocation.


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