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Results and discussion

Segregation for seedling reactions in F2 and F3 generations and its intercross obtained from the crosses of resistant cultivars with Malvi Local are given in
Table 2. The F2 and F3 generations obtained from the cross Malvika x Malvi Local segregated in a 15 resistant (R): 1 susceptible (S) ratio and in a 7 homozygous resistant (HR): 8 segregating (Seg): 1 homozygous susceptible (HS) ratio against race 1, respectively. This indicates the presence of two independently inherited dominant genes in Malvika against the race 1. The F2 and F3 generations obtained from the cross CPAN 6051 x Malvi Local segregated in an 3R : 1S ratio and in a 1 HR : 2 Seg : 1 HS ratio respectively indicating presence of one dominant gene against race 1. Against race 77A, the F2 and F3 generations obtained from the crosses Malvika x Malvi Local and CPAN 6051 x Malvi Local segregated in a 15R : 1S ratio and in a 7 HR : 8 Seg : 1 HS ratio. These observations indicated presence of two independently inherited dominant genes in Malvika against race 77A. The F2 and F3 generations from the cross CPAN 6051 x Malvi Local segregated in a 3R : 1S ratio and 1HR : 2 Seg : 1HS ratio, respectively, indicating presence of a dominant gene in CPAN 6051 against race 108.

Susceptible seedlings against races 1, 77A and 108 were not observed in F2 generation obtained from the cross Malvika x CPAN 6051, indicating that at least one of the genes present in Malvika and CPAN 6051 is allelic or tightly linked.

Inheritance studies and allelic tests revealed the presence of at least two different leaf rust resistance genes from cultivars Malvika and CPAN 6051.
Since the near isogenic testers are not available in durum. background it is not possible to designate Lr genes in any of these two wheats. Saini (1987) has identified Lr23 from CPAN 6051 using Australian rust cultures. Since CPAN 6051 did not segregate for susceptible seedling against race 1 in its cross with Malvika therefore this cultivar may also have Lr23. This gene gives post seedling resistance against races 77A and 108 (Saini et al 1988, Dhindsa et al 1991), therefore, resistance of both these cultivars in epiphytotic of race 77A may be due to Lr23. The other gene conferring resistance to races 77A and 108 in seedlings of CPAN 6051 needs to be identified as yet. Although virulence against Lr23 is now available in the Indian subcontinent (Nayer et al 1988), the other gene(s) from these wheats are still effective and can be used in breeding programmes.

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