Linkage between the Lr10 gene conditioning resistance to leaf rust, two endosperm proteins, and hairy glumes in hexaploid wheat

1986 ◽  
Vol 28 (4) ◽  
pp. 595-600 ◽  
Author(s):  
N. K. Howes

The possibility that genes controlling the expression of wheat endosperm proteins are linked to the Lr10 gene conditioning resistance to leaf rust (Puccinia recondita f. sp. tritici) race 1 was examined. Derived F3 progeny lines from a cross between two hexaploid spring wheat cultivars (Triticum aestivum) 'Little Club' and line 'Prelude' Lr10 (RL6004), segregated for the Lr10 gene, gliadin component band 50 (54 kilodalton, kDa), a nongliadin endosperm protein (70 kDa), and hairy glumes (Hg). These four characters were each monogenically inherited and were linked, with the gene order being Lr10, (54 and 70 kDa polypeptides), Hg. These genes are located on the short arm of chromosome 1A. The genes Hg and Lr10 could be useful flanking markers to study the fine structure of the complex Gli-A1 locus.Key words: leaf rust, gliadins, glumes (hairy).

1977 ◽  
Vol 19 (2) ◽  
pp. 355-358 ◽  
Author(s):  
P. L. Dyck ◽  
E. R. Kerber

The inheritance of seedling resistance to leaf rust (Puccinia recondita) was studied in wheat (Triticum aestivum L.) cultivars Rafaela and EAP 26127. Rafaela has genes Lr14b and Lr17 while EAP 26127 has Lr17. Lr17 was located on chromosome 2A, possibly the short arm, and was independent of Lr11.


1989 ◽  
Vol 69 (4) ◽  
pp. 1113-1117 ◽  
Author(s):  
P. L. DYCK

The genetics of resistance to leaf rust (Puccinia recondita f. sp. tritici) was studied in the two common wheat (Triticum aestivum) cultivars Kenyon and Buck Manantial. Kenyon was shown to have genes Lr13 and Lr16, the same gene combination that is present in the cultivar Columbus. Buck Manantial, the leaf-rust resistant donor parent of Kenyon, has seedling genes Lr13 (or an allele), Lr16 and Lr17, and two for adult-plant resistance, Lr13 and an unidentified gene.Key words: Leaf rust resistance, Puccinia recondita f. sp. tritici, wheat (hard red spring)


1984 ◽  
Vol 26 (6) ◽  
pp. 736-742 ◽  
Author(s):  
R. P. Singh ◽  
R. A. McIntosh

Two complementary genes, A and B, conferring resistance to Puccinia recondita tritici in various wheats were located in chromosomes 4Aβ and 3BS, respectively. In one study gene B showed recombination of 33.6 ± 4.1% with the centromere, and was independent in a second study. Gene B was the same as that designated Lr27. A new designation, Lr31, is proposed for gene A. Both Lr27 and Lr31 must be present for the expression of resistance.Key words: leaf rust, monosomic analysis, aneuploids, wheat.


1977 ◽  
Vol 19 (4) ◽  
pp. 711-716 ◽  
Author(s):  
P. L. Dyck

The genetics of seedling resistance to leaf rust (Puccinia recondita Rob. ex. Desm.) was investigated in what (Triticum aestivum L.) introductions PI 268454, PI 58548 and PI 268316, originally collected in Afghanistan, China and Iran, respectively. PI 268454 was heterogeneous for resistance. A selection (PI 268454a) has a gene that confers a 1+ reaction while a second selection (PI 268454b) probably has resistance gene Lr2b. PI 58548 has two genes for resistance, one giving a 1+ reaction and the second a 2+. These two genes interact to produce a; 1 reaction. PI 268316 has three interacting genes, one giving a 1+ reaction, the second a 2+ and a third resistance gene similar to LrB. The gene giving the 1+ reaction was common to all three introductions. PI 58548 and PI 268316 carry different genes for infection type 2+. Backcross lines of the single genes were produced. Implications to breeding for disease resistance of genes interacting to produce different phenotype are discussed.


Genome ◽  
1987 ◽  
Vol 29 (2) ◽  
pp. 365-366 ◽  
Author(s):  
G. C. Eizenga

Twelve lines of wheat (Triticum aestivum L.) were originally identified as having a segment of Agropyron elongatum chromatin carrying a gene for resistance to leaf rust (Puccinia recondita tritici) transferred to wheat chromosome 7D. By studying the chromosome pairing of one of these lines, transfer no. 12, with telosomes 7AL, 7AS, 7BL, 7BS, 7DL, 7DS, and 7AgS, it was determined that the Agropyron chromatin was carried on the long arm of wheat chromosome 7A rather than 7D. This determination was confirmed by acetocarmine–N-banding. Key words: Triticum aestivum, Agropyron elongatum, transfer lines, Puccinia recondita tritici, telosomic analysis.


1997 ◽  
Vol 75 (12) ◽  
pp. 2082-2096 ◽  
Author(s):  
Y. Anikster ◽  
W. R. Bushnell ◽  
A. P. Roelfs ◽  
T. Eilam ◽  
J. Manisterski

Aecial and telial host range, interfertility, teliospore dimensions, and amount of nuclear DNA were determined for Puccinia recondita collected either worldwide from species of cultivated wheats (Triticum aestivum and Triticum turgidum ssp. durum and rye (Secale cereale), or from wild emmer (Triticum turgidum ssp. dicoccoides) and four species of wild wheat (Aegilops) in Israel. The results indicate that the collections belong in two major groups: Group I (from cultivated wheats and wild emmer), which has Thalictrum speciosissimum (in the Ranunculaceae) as principal aecial host; and Group II (principally from wild wheats or rye), which has several species in the Boraginaceae, such as Anchusa aggregata, Anchusa italica, Echium glomeratum, and Lycopsis arvensis as aecial hosts. In glasshouse experiments, intercrosses could be made readily among collections within Groups I and II but not between the two groups. Group I consisted of all collections from Triticum aestivum, Triticum turgidum ssp. dicoccoides, and most collections from Triticum turgidum ssp. durum. For Group I collections, four species of Aegilops, Hordeum maritimum, S. cereale, as well as Triticum aestivum and Triticum turgidum ssp. durum and ssp. dicoccoides could all serve as telial host in glasshouse experiments. Group II consisted of four types, all clearly different from Group I. Type A was from Triticum turgidum ssp. durum found in fields near Anchusa italica, which was its only aecial host; Triticum aestivum, Triticum turgidum ssp. durum, and Triticum turgidum ssp. dicoccoides could serve as telial hosts. Type B was from Aegilops ovata and had E. glomeratum, Anchusa undulata, and L. arvensis as aecial hosts. Type C was from Aegilops longissima, Aegilops sharonensis, and Aegilops variabilis and had Anchusa aggregata, Anchusa undulata and L. arvensis as aecial hosts. Type D was from S. cereale and had L. arvensis and Anchusa undulata as aecial hosts. In addition to differences in host range, teliospores were wider and bigger in cross sectional area, and nuclear DNA content of pycniospores was 1.3–1.6 times greater in Group II than in Group I. The results suggest that Groups I and II have evolved separately for an extended period and are now morphologically distinct and genetically isolated from each other. Furthermore, differences in both telial and aecial host species, in teliospore dimensions, and in amount of nuclear DNA indicate that subgroups within Group II are beginning to show genetic divergence. Key words: aecial hosts, Aegilops, Anchusa, Echium, Hordeum, leaf rust, Lycopsis, Puccinia recondita, Puccinia triticina, Secale, Thalictrum, Triticum.


1979 ◽  
Vol 30 (3) ◽  
pp. 421 ◽  
Author(s):  
RG Rees ◽  
JP Thompson ◽  
EA Goward

The progress and effects of epidemics of leaf rust (Puccinia recondita Rob, ex Desm. f, sp. tritici Erikss. & Henn.) have been examined in 45 wheat cultivars over two seasons. The epidemics in each cultivar were compared by various measures and by pattern analysis. The cultivars were separated into groups ranging from highly resistant to highly susceptible with intermediate groups possessing various levels of slow-rusting ability. Cvv. Hopps, Warchief, Huguenot, Pusa 80-5c, Dural, Warput, Koolisie and Puglu were found to possess useful levels of slow-rusting ability. Fast rusting was conspicuous in Gabo and its derivatives Mendos, Mengavi, Gamenya and Gamut. The desirability of not perpetuating this defect is discussed.


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