scholarly journals Molecular detection of disease resistance genes to powdery mildew (Blumeria graminis f. sp. tritici) in wheat (Triticum aestivum) cultivars

2017 ◽  
Vol 16 (1) ◽  
pp. 22-31 ◽  
Author(s):  
Mgoli Mwale Vincent ◽  
Tang Xiuli ◽  
Chilembwe Eric
Keyword(s):  
Triticum Aestivum ◽  
Disease Resistance ◽  
Powdery Mildew ◽  
Resistance Genes ◽  
Molecular Detection ◽  
Blumeria Graminis ◽  
Disease Resistance Genes

scholarly journals Comparison of groups of Triticum aestivum L. varieties of the Steppe and the Forest-Steppe of Ukraine by markers for important genes

1970 ◽  
Vol 21 ◽  
pp. 193-198
Author(s):  
I. O. Sozinov ◽  
N. O. Kozub ◽  
A. V. Karelov ◽  
L. A. Pylypenko ◽  
H. Ya. Bidnyk ◽  
...  
Keyword(s):  
Triticum Aestivum ◽  
Disease Resistance ◽  
Resistance Genes ◽  
Storage Protein ◽  
Storage Proteins ◽  
Triticum Aestivum L ◽  
Disease Resistance Genes ◽  
Pcr Analysis ◽  
Forest Steppe ◽  
Disease Resistance Gene

Aim. The aim of the study was to compare diversity of groups of winter common wheat varieties of the Steppe and the Central Forest-Steppe of Ukraine by storage protein loci and some disease resistance genes and to reveal peculiarities of varieties released after 1995. Methods. SDS and APAG electrophoresis was used to identify genotypes at the Glu-1, Gli-1, and some minor gliadin loci. PCR analysis was employed to study alleles of the disease resistance genes Lr34/Yr18/Pm38/Sr57/Bdv1, Tsn1, Tsc2, TDF_076_2D, and Cre-8. Results. Significant differences in frequencies of alleles at most marker loci were revealed. Nonrandom associations between disease resistance gene alleles as well as storage protein alleles were detected. Conclusions. The retention of a set of predominant alleles of a certain zone in different periods of breeding was confirmed. The appearance of new allele associations in the groups of varieties of the Steppe (in particular Gli-A1g and Glu-B1al) and the Central Forest-Steppe (1AL/1RS and Glu-B1d) in the last two decades was noted. Keywords: Triticum aestivum L., varieties, storage proteins, resistance genes, alleles.

RFLP markers linked to powdery mildew resistance genes Pm1, Pm2, Pm3, and Pm4 in wheat

Genome ◽  
1994 ◽  
Vol 37 (5) ◽  
pp. 871-875 ◽  
Author(s):  
Z. Q. Ma ◽  
M. E. Sorrells ◽  
S. D. Tanksley
Keyword(s):  
Triticum Aestivum ◽  
Powdery Mildew ◽  
Resistance Genes ◽  
Polymorphic Locus ◽  
Triticum Aestivum L ◽  
Blumeria Graminis ◽  
Rflp Markers ◽  
Recurrent Parent ◽  
Polymorphic Markers ◽  
Restriction Fragment Length Polymorphic

Near-isogenic lines (NILs) and their recurrent parent Chancellor (Cc) were used to identify restriction fragment length polymorphic markers linked to powdery mildew (Blumeria graminis (DC.) E.O. Speer f.sp. tritici) resistance genes Pm1, Pm2, Pm3, and Pm4 in wheat (Triticum aestivum L. em. Thell). By mapping these polymorphic markers in F2 progenies from crosses of the NILs with Cc, it was found that Pm1 cosegregated with a polymorphic locus detected by DNA probe CDO347; Pm2 was linked to a locus detected by probe BCD1871 with a distance of 3.5 cM; Pm3b was linked to a locus detected by probe BCD1434 with a distance of 1.3 cM; Pm4a cosegregated with Xbcd1231-2A(2) and Xcdo678-2A, and was closely flanked by Xbcd1231-2A(1) and Xbcd292-2A both with a distance of 1.5 cM. Aneuploid mapping of these markers indicated that locus Xcdo347-7A is on 7AL, Xbcd1871-5D on 5DS, Xbcd1434-1A on 1AS, and loci Xbcd292-2A and Xcdo678-2A are on 2AL. The same polymorphic fragments detected in the Pm3b NIL by Xbcd1434-1A were found in Pm3a NIL using several enzyme digestions.Key words: RFLP markers, Pm1, Pm2, Pm3, Pm4, Blumeria graminis (DC.) E.O. Speer f.sp. tritici (Erysiphe graminis f.sp. tritici), wheat (Triticum aestivum L. em. Thell), gene tagging.

scholarly journals Recognition Specificity and RAR1/SGT1 Dependence in Barley Mla Disease Resistance Genes to the Powdery Mildew Fungus

2003 ◽  
Vol 15 (3) ◽  
pp. 732-744 ◽  
Author(s):  
Qian-Hua Shen ◽  
Fasong Zhou ◽  
Stephane Bieri ◽  
Thomas Haizel ◽  
Ken Shirasu ◽  
...  
Keyword(s):  
Disease Resistance ◽  
Powdery Mildew ◽  
Resistance Genes ◽  
Disease Resistance Genes ◽  
Powdery Mildew Fungus ◽  
Recognition Specificity

scholarly journals Variability of the wheat powdery mildew pathogen Blumeria graminis f. sp. tritici in the 2003 crop season

2005 ◽  
Vol 30 (4) ◽  
pp. 420-422 ◽  
Author(s):  
Leila M. Costamilan
Keyword(s):  
Triticum Aestivum ◽  
Powdery Mildew ◽  
Resistance Genes ◽  
Genetic Resistance ◽  
Blumeria Graminis ◽  
Wheat Cultivars ◽  
Crop Season ◽  
Grain Yields ◽  
Wheat Powdery Mildew ◽  
Powdery Mildew Pathogen

Wheat (Triticum aestivum) powdery mildew, caused by the biotrophic fungus Blumeria graminis f. sp. tritici, is one of the most severe foliar diseases attacking this crop, reducing grain yields by 10% to 62% in Brazil. The disease can be controlled by genetic resistance of the host, but the pathogen has physiological specialization, which enables it to infect wheat cultivars that have remained resistant for years. The objective of this work was to evaluate the variability of pathogenic strains of B. graminis f. sp. tritici collected in Brazil and the effectiveness of wheat resistance genes to powdery mildew in the 2003 crop season. Plants of a differential series were inoculated with each monopustular isolate. Thirty-one combinations of effective and ineffective resistance genes were identified. Only the gene Pm4a+... remained totally effective to all isolates, and gene Pm6 was highly effective (below 10% of susceptibility), whereas genes Pm3a and Pm8 were totally ineffective (susceptible to all isolates). Genes Pm3c, D1, and D2 showed low effectiveness (above 50% of susceptibility), and genes Pm1, 2, 4a, 1+?, and 2+Mld had mean effective results to most strains (susceptibility between 10% and 49%). The virulence formula Pm1, 3c, 4a, 6, 1+?, 2+Mld, 4a+..., D2 (effective genes) / 2, 3a, 8, D1 (ineffective genes) was most frequently found, accounting for 15% of the occurrences. The most frequent number of ineffective genes was seven, ranging from three to ten.

Genome-Wide Analysis of NBS-Encoding Disease Resistance Genes in Maize Inbred Line B73

2009 ◽  
Vol 35 (3) ◽  
pp. 566-570 ◽  
Author(s):  
Jie-Ming WANG ◽  
Hai-Yang JIANG ◽  
Yang ZHAO ◽  
Yan XIANG ◽  
Su-Wen ZHU ◽  
...  
Keyword(s):  
Disease Resistance ◽  
Inbred Line ◽  
Resistance Genes ◽  
Disease Resistance Genes ◽  
Maize Inbred Line ◽  
Genome Wide Analysis ◽  
Genome Wide

Comparative Mapping of Three Bacterial, Three Fungal, and One Virus Disease-resistance Genes in Common Bean

HortScience ◽  
1998 ◽  
Vol 33 (3) ◽  
pp. 547a-547
Author(s):  
Geunhwa Jung ◽  
James Nienhuis ◽  
Dermot P. Coyne ◽  
H.M. Ariyarathne
Keyword(s):  
Disease Resistance ◽  
Common Bean ◽  
Pseudomonas Syringae ◽  
Resistance Genes ◽  
Fungal Pathogens ◽  
Xanthomonas Campestris ◽  
Virus Disease ◽  
Disease Resistance Genes ◽  
Brown Spot ◽  
Viral Pathogen

Common bacterial blight (CBB), bacterial brown spot (BBS), and halo blight (HB), incited by the bacterial pathogens Xanthomonas campestris pv. phaseoli (Smith) Dye, Pseodomonas syringae pv. syringa, and Pseudomonas syringae pv. phaseolicola, respectively are important diseases of common bean. In addition three fungal pathogens, web blight (WB) Thanatephorus cucumeris, rust Uromyces appendiculatus, and white mold (WM) Sclerotinia sclerotiorum, are also destructive diseases attacking common bean. Bean common mosaic virus is also one of most major virus disease. Resistance genes (QTLs and major genes) to three bacterial (CBB, BBS, and HB), three fungal (WB, rust, and WM), and one viral pathogen (BCMV) were previously mapped in two common bean populations (BAC 6 × HT 7719 and Belneb RR-1 × A55). The objective of this research was to use an integrated RAPD map of the two populations to compare the positions and effect of resistance QTL in common bean. Results indicate that two chromosomal regions associated with QTL for CBB resistance mapped in both populations. The same chromosomal regions associated with QTL for disease resistance to different pathogens or same pathogens were detected in the integrated population.

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