resistance gene homologue
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2004 ◽  
Vol 54 (2) ◽  
pp. 533-545 ◽  
Author(s):  
Nienke Westerink ◽  
Bas F. Brandwagt ◽  
Pierre J. G. M. De Wit ◽  
Matthieu H. A. J. Joosten

2004 ◽  
Vol 161 (7) ◽  
pp. 815-822 ◽  
Author(s):  
Bangjun Wang ◽  
Yongjun Wang ◽  
Qiang Wang ◽  
Guangzuo Luo ◽  
Zhigang Zhang ◽  
...  

Genetics ◽  
1999 ◽  
Vol 153 (4) ◽  
pp. 1929-1948 ◽  
Author(s):  
Fusheng Wei ◽  
Karin Gobelman-Werner ◽  
Shaun M Morroll ◽  
Joachim Kurth ◽  
Long Mao ◽  
...  

Abstract Powdery mildew of barley, caused by Erysiphe graminis f. sp. hordei, is a model system for investigating the mechanism of gene-for-gene interaction between large-genome cereals and obligate-fungal pathogens. A large number of loci that confer resistance to this disease are located on the short arm of chromosome 5(1H). The Mla resistance-gene cluster is positioned near the telomeric end of this chromosome arm. AFLP-, RAPD-, and RFLP-derived markers were used to saturate the Mla region in a high-resolution recombinant population segregating for the (Mla6 + Mla14) and (Mla13 + Ml-Ru3) resistance specificities. These tightly linked genetic markers were used to identify and develop a physical contig of YAC and BAC clones spanning the Mla cluster. Three distinct NBS-LRR resistance-gene homologue (RGH) families were revealed via computational analysis of low-pass and BAC-end sequence data derived from Mla-spanning clones. Genetic and physical mapping delimited the Mla-associated, NBS-LRR gene families to a 240-kb interval. Recombination within the RGH families was at least 10-fold less frequent than between markers directly adjacent to the Mla cluster.


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