7 research outputs found

    Response of 150 F6 inbred durum wheat lines derived from Kunduru-1149×Cham-1 cross to yellow rust (Puccinia striiformis)

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    One hundred and fifty F6 inbred durum wheat lines derived from Kunduru-1149 x Cham-1 cross were characterised in terms of their response to yellow rust (Puccinia striiformis) race population including Yr2, Yr6, Yr7 and Yr9 virulence genes. The results revealed that there is a considerable amount of genetic variation among these lines and yellow rust resistance in durum wheat is highly heritable (92%). Twenty-five of 150 lines (16.67%) were found totally immune, 104 of them (69.33%) were found to be resistant or moderately resistant while only 21 of them (14%) were found to be susceptible. Hence, 86% of the lines tested in this study could be used as a source of yellow rust resistance in breeding programmes

    Yr10 gene polymorphism in bread wheat varieties

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    Yellow rust resistance locus Yr10 located on chromosome 1B in Moro and originated from the Turkish line PI178383 was investigated in terms of polymorphism in seven winter type bread wheat cvs.(Triticum aestivum ssp. Aestivum) Altay2000, zgi2001, Sönmez2001 (yellow rust resistant), Aytýn98, ES14, Harmankaya99 (yellow rust susceptible) and PI178383 as control. Exon 1 (1 - 833 bp) and Exon 2 (1989 - 3630 bp) parts of Yr10 were amplified with three primers. Amplification was not observed with E2A primers in Harmankaya99, zgi2001 and Sönmez2001 cvs, while amplification products were observable at all tested varieties with the other primers. PCR results showed that E2A reverse primer is not able to anneal to the three varieties mentioned above. Sequence analysis and bioinformaticsanalysis proved that there has been single nucleotide changes especially in the second exon. The most similar sequences to the first exon of Harmankaya99, zgi01 and Sönmez2001 are AF509535 (Aegilops tauschii NBS-LRR-like gene), AF509534 (A. tauschii NBS-LRR-like gene sequence) and AF509534, respectively. These results could be helpful in revealing divergence between resistant and susceptible varieties

    Yr10 gene polymorphism in bread wheat varieties

    No full text
    Yellow rust resistance locus Yr10 located on chromosome 1B in Moro and originated from the Turkish line PI178383 was investigated in terms of polymorphism in seven winter type bread wheat cvs. (Triticum aestivum ssp. Aestivum) Altay2000, zgi2001, Sönmez2001 (yellow rust resistant), Aytın98, ES14, Harmankaya99 (yellow rust susceptible) and PI178383 as control. Exon 1 (1 -833 bp) and Exon 2 (1989 -3630 bp) parts of Yr10 were amplified with three primers. Amplification was not observed with E2A primers in Harmankaya99, zgi2001 and Sönmez2001 cvs, while amplification products were observable at all tested varieties with the other primers. PCR results showed that E2A reverse primer is not able to anneal to the three varieties mentioned above. Sequence analysis and bioinformatics analysis proved that there has been single nucleotide changes especially in the second exon. The most similar sequences to the first exon of Harmankaya99, zgi01 and Sönmez2001 are AF509535 (Aegilops tauschii NBS-LRR-like gene), AF509534 (A. tauschii NBS-LRR-like gene sequence) and AF509534, respectively. These results could be helpful in revealing divergence between resistant and susceptible varieties

    Yr10 gene polymorphism in bread wheat varieties

    No full text
    Yellow rust resistance locus Yr10 located on chromosome 1B in Moro and originated from the Turkish line PI178383 was investigated in terms of polymorphism in seven winter type bread wheat cvs. (Triticum aestivum ssp.Aestivum) Altay2000, İzgi2001, Sönmez2001 (yellow rust resistant), Aytın98, ES14, Harmankaya99 (yellow rust susceptible) and PI178383 as control. Exon 1 (1 - 833 bp) and Exon 2 (1989 - 3630 bp) parts of Yr10 were amplified with three primers. Amplification was not observed with E2A primers in Harmankaya99, İzgi2001 and Sönmez2001 cvs, while amplification products were observable at all tested varieties with the other primers. PCR results showed that E2A reverse primer is not able to anneal to the three varieties mentioned above. Sequence analysis and bioinformatics analysis proved that there has been single nucleotide changes especially in the second exon. The most similar sequences to the first exon of Harmankaya99, İzgi01 and Sönmez2001 are AF509535 (Aegilops tauschiiNBS-LRR-like gene), AF509534 (A. tauschii NBS-LRR-like gene sequence) and AF509534, respectively. These results could be helpful in revealing divergence between resistant and susceptible varieties
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