scholarly journals Leaf Rust Resistance Gene Lr34 Associated with Nonsuppression of Stem Rust Resistance in the Wheat Cultivar Canthatch

1999 ◽  
Vol 89 (6) ◽  
pp. 518-521 ◽  
Author(s):  
E. R. Kerber ◽  
T. Aung

The common wheat cultivar Thatcher and the backcross derivative Canthatch are moderately or fully susceptible to several races of stem rust because of a suppressor on chromosome 7DL that inhibits the expression of the relevant resistance gene(s). The incorporation of leaf rust resistance gene Lr34 into ‘Thatcher’ is known to enhance stem rust resistance. The effect of this gene in a ‘Canthatch’ background and its relationship with the 7DL suppressor were determined by replacing chromosome 7D of ‘Canthatch’ with 7D of ‘Chinese Spring’, which possesses Lr34 on the short arm. ‘Canthatch’ nullisomic 7D was crossed with ‘Chinese Spring’, followed by a succession of backcrosses to the nullisomic recurrent parent. Homozygous resistant disomic and monosomic substitution lines were recovered that exhibited the same resistant reaction as that of ‘Thatcher’ possessing Lr34 and as that of ‘Canthatch’ nullisomic 7D, in which the 7DL suppressor is absent. The results indicate that, in ‘Canthatch’, Lr34 permits expression of resistance genes normally inhibited by the 7DL suppressor. Furthermore, it is likely that, in ‘Thatcher’ and ‘Thatcher’ back-cross derivatives, Lr34 inactivates the 7DL suppressor.

2018 ◽  
Vol 54 (No. 2) ◽  
pp. 65-70
Author(s):  
Y. Zhou ◽  
H. Li ◽  
P.-P. Zhang ◽  
L. Wang ◽  
Z.-F. Li

Leaf rust, caused by Puccinia triticina, is a major wheat disease worldwide. The chinese wheat cultivar L224-3 showed high resistance to most of P. triticina pathotypes in the seedling and adult stage. Identifying and mapping the leaf rust resistance gene(s) in L224-3 is very useful for breeding leaf rust resistant wheat cultivars. In the present study, the wheat cultivar L224-3 and thirty-six lines with known leaf rust resistance genes were inoculated with 15 pathotypes at the seedling stage for gene postulation. A total of 144 F<sub>2:3</sub> lines from the cross L224-3 × Zhengzhou 5389 were inoculated with the pathotype FHBQ for leaf rust genetic analysis at the seedling stage. A total of 1276 SSR (simple sequence repeat) markers and the STS (sequence tagged-site) marker ω-secali/Glu-B3 were used to test the parents, resistant and susceptible bulks. The polymorphic markers were used to genotype the F<sub>2:3</sub> populations. L224-3 was highly resistant to all Lr26 avirulent pathotypes, showing the presence of Lr26 in L224-3. The presence of Lr26 in L224-3 was also confirmed by the molecular marker ω-secalin/Glu-B3. Due to resistance to some Lr26 virulent pathotypes, L224-3 may carry another resistance gene. Based on the genetic analysis using the pathotype FHBQ with virulence to Lr26 the resistance of L224-3 was controlled by a single dominant gene, tentatively designated LrL224. Four SSR markers (barc8, gwm582, wmc419, and wmc694) and one STS marker (ω-secali/Glu-B3) on 1B were closely linked to LrL224. The two flanking SSR loci were barc8 and gwm582, with the genetic distances of 4.3 and 4.6 cM, respectively. LrL224 was located on 1BL, and it showed different seedling reactions with other genes on 1B. Therefore LrL224 is likely to be a new leaf rust resistance gene.


2010 ◽  
Vol 28 (4) ◽  
pp. 527-534 ◽  
Author(s):  
Hai Zhang ◽  
Xianchun Xia ◽  
Zhonghu He ◽  
Xing Li ◽  
Zaifeng Li ◽  
...  

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

Crop Science ◽  
2003 ◽  
Vol 43 (1) ◽  
pp. 388 ◽  
Author(s):  
J. A. Mammadov ◽  
J. C. Zwonitzer ◽  
R. M. Biyashev ◽  
C. A. Griffey ◽  
Y. Jin ◽  
...  

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