Association of Storage Protein Patterns and Leaf Rust Resistance Derived From Aegilops umbellulata Zhuk. in the Wheat

1998 ◽  
Vol 26 (4) ◽  
pp. 471-478
Author(s):  
Tsvetana Stoilova ◽  
Antoaneta Yankova
Keyword(s):  
Leaf Rust ◽  
Storage Protein ◽  
Rust Resistance ◽  
Leaf Rust Resistance ◽  
Protein Patterns ◽  
Aegilops Umbellulata

Development and validation of molecular markers linked to an Aegilops umbellulata–derived leaf-rust-resistance gene, Lr9, for marker-assisted selection in bread wheat

Genome ◽  
2005 ◽  
Vol 48 (5) ◽  
pp. 823-830 ◽  
Author(s):  
Sudhir Kumar Gupta ◽  
Ashwini Charpe ◽  
Sunita Koul ◽  
Kumble Vinod Prabhu ◽  
Qazi Mohd. Rizwanul Haq
Keyword(s):  
Leaf Rust ◽  
Resistance Gene ◽  
Rust Resistance ◽  
Scar Marker ◽  
Rapd Marker ◽  
Gene Pyramiding ◽  
Leaf Rust Resistance ◽  
Rust Resistance Gene ◽  
Leaf Rust Resistance Gene ◽  
Aegilops Umbellulata

An Aegilops umbellulata–derived leaf-rust-resistance gene, Lr9, was tagged with 3 random amplified polymorphic DNA (RAPD) markers, which mapped within 1.8 cM of gene Lr9 located on chromosome 6BL of wheat. The markers were identified in an F2 population segregating for leaf-rust resistance, which was generated from a cross between 2 near-isogenic lines that differed in the alien gene Lr9 in a widely adopted agronomic background of cultivar 'HD 2329'. Disease phenotyping was done in controlled environmental conditions by inoculating the population with the most virulent pathotype, 121 R63-1 of Puccinia triticina. One RAPD marker, S5550, located at a distance of 0.8 ± 0.008 cM from the Lr9 locus, was converted to sequence-characterized amplified region (SCAR) marker SCS5550. The SCAR marker was validated for its specificity to gene Lr9 against 44 of the 50 known Lr genes and 10 wheat cultivars possessing the gene Lr9. Marker SCS5550 was used with another SCAR marker, SCS73719, previously identified as being linked to gene Lr24 on a segregating F2 population to select for genes Lr9 and Lr24, respectively, demonstrating the utility of the 2 markers in marker-assisted gene pyramiding for leaf-rust resistance in wheat.Key words: wheat, leaf rust resistance, Lr9, Lr24, RAPD, SCAR.

Linkage relations of Gli-D1, Rg2, and Lr21 on the short arm of chromosome 1D in wheat

Genome ◽  
1990 ◽  
Vol 33 (6) ◽  
pp. 937-940 ◽  
Author(s):  
S. S. Jones ◽  
J. Dvořák ◽  
C. O. Qualset
Keyword(s):  
Triticum Aestivum ◽  
Leaf Rust ◽  
Storage Protein ◽  
Chinese Spring ◽  
Rust Resistance ◽  
Storage Proteins ◽  
Seed Storage Protein ◽  
Leaf Rust Resistance ◽  
Triticum Tauschii ◽  
Chromosome Arm

Homozygous recombinant substitution lines, derived from a cross of Triticum aestivum 'Chinese Spring' with a disomic substitution line of Triticum tauschii chromosome 1D in 'Chinese Spring', were used to investigate the linkage relationships among the loci Glu-D1, encoding high molecular weight glutenin storage proteins, Gli-D1, encoding gliadin storage proteins, Rg2, controlling glume color, and Lr21, conferring leaf-rust resistance. Gli-D1, on chromosome arm 1DS, is tightly linked to Rg2 and Lr21 (1.4 and 5.6% recombination, respectively). The order of the loci is Gli-D1–Rg2–Lr21. Glu-D1, on chromosome arm 1DL, segregates independently (P = 0.43) of Gli-D1, Rg2, and Lr21. The position of Glu-D1, Gli-D1, Rg2, and Lr21 in the genetic linkage map of chromosome 1D agrees with the position of storage protein, glume color, and rust-resistance loci on chromosomes 1A and 1B.Key words: leaf-rust resistance, seed storage protein, glutenin, gliadin, glume color, Triticum aestivum, Triticum tauschii.

Lr80: A new and widely effective source of leaf rust resistance of wheat for enhancing diversity of resistance among modern cultivars

2021 ◽  
Author(s):  
Subodh Kumar ◽  
Subhash C. Bhardwaj ◽  
Om P. Gangwar ◽  
Akanksha Sharma ◽  
Naeela Qureshi ◽  
...  
Keyword(s):  
Leaf Rust ◽  
Rust Resistance ◽  
Leaf Rust Resistance ◽  
Effective Source

scholarly journals Map-Based Cloning of Leaf Rust Resistance Gene Lr21 From the Large and Polyploid Genome of Bread Wheat

Genetics ◽  
2003 ◽  
Vol 164 (2) ◽  
pp. 655-664 ◽  
Author(s):  
Li Huang ◽  
Steven A Brooks ◽  
Wanlong Li ◽  
John P Fellers ◽  
Harold N Trick ◽  
...  
Keyword(s):  
Amino Acid ◽  
Leaf Rust ◽  
Resistance Gene ◽  
Bread Wheat ◽  
Rust Resistance ◽  
Agronomic Traits ◽  
Leaf Rust Resistance ◽  
Triticum Aestivum L ◽  
Rust Resistance Gene ◽  
Leaf Rust Resistance Gene

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.

scholarly journals Identification of leaf rust resistance genes Lr34 and Lr46 in common wheat (Triticum aestivum L. ssp. aestivum) lines of different origin using multiplex PCR

2021 ◽  
Vol 16 (1) ◽  
pp. 172-183
Author(s):  
Agnieszka Tomkowiak ◽  
Roksana Skowrońska ◽  
Michał Kwiatek ◽  
Julia Spychała ◽  
Dorota Weigt ◽  
...  
Keyword(s):  
Multiplex Pcr ◽  
Leaf Rust ◽  
Common Wheat ◽  
Fungal Pathogens ◽  
Rust Resistance ◽  
Leaf Rust Resistance ◽  
Field Conditions ◽  
Pcr Marker ◽  
Specific Sequence ◽  
Cereal Species

Abstract Leaf rust caused by the fungus Puccinia recondita f. sp. tritici is one of the most dangerous diseases of common wheat. Infections caused by fungal pathogens reduce the quantity and quality of yields of many cereal species. The most effective method to limit plant infection is to use cultivars that show rust resistance. Genetically conditioned horizontal-type resistance (racial-nonspecific) is a desirable trait because it is characterized by more stable expression compared to major (R) genes that induce racially specific resistance, often overcome by pathogens. Horizontal resistance is conditioned by the presence of slow rust genes, which include genes Lr34 and Lr46. This study aimed to identify markers linked to both genes in 64 common wheat lines and to develop multiplex PCR reaction conditions that were applied to identify both genes simultaneously. The degree of infestation of the analyzed lines was also assessed in field conditions during the growing season of 2017 and 2018. Simple sequence repeat anchored-polymerase chain reaction (SSR-PCR) marker csLV was identified during analysis in line PHR 4947. The presence of a specific sequence has also been confirmed in multiplex PCR analyses. In addition to gene Lr34, gene Lr46 was identified in this genotype. Lines PHR 4947 and PHR 4819 were characterized by the highest leaf rust resistance in field conditions. During STS-PCR analyses, the marker wmc44 of gene Lr46 was identified in most of the analyzed lines. This marker was not present in the following genotypes: PHR 4670, PHR 4800, PHR 4859, PHR 4907, PHR 4922, PHR 4949, PHR 4957, PHR 4995, and PHR 4997. The presence of a specific sequence has also been confirmed in multiplex PCR analyses. Genotypes carrying the markers of the analyzed gene showed good resistance to leaf rust in field conditions in both 2017 and 2018. Research has demonstrated that marker assisted selection (MAS) and multiplex PCR techniques are excellent tools for selecting genotypes resistant to leaf rust.

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