In addition to drought and extreme temperatures, soil salinity represents a growing threat to crop productivity. Among the cereal crops, barley is considered as notably salt tolerant, and cultivars show considerable variation for tolerance towards salinity stress. In order to unravel the molecular mechanisms underlying salt stress tolerance and to utilize the natural genetic variation of barley accessions, a series of hydroponics-based salinity stress experiments was conducted using two genetic mapping parents, cvs Steptoe and Morex, which display contrasting levels of salinity tolerance. The proteome of roots from both genotypes was investigated as displayed by two-dimensional gel electrophoresis, and comparisons were made between plants grown under non-saline and saline conditions. Multivariate analysis of the resulting protein patterns revealed cultivar-specific and salt stress-responsive protein expression. Mass spectrometry-based identification was successful for 26 out of 39 selected protein spots. Hierarchical clustering was applied to detect similar protein expression patterns. Among those, two proteins involved in the glutathione-based detoxification of reactive oxygen species (ROS) were more abundant in the tolerant genotype, while proteins involved in iron uptake were expressed at a higher level in the sensitive one. This study emphasizes the role of proteins involved in ROS detoxification during salinity stress, and identified potential candidates for increasing salt tolerance in barley.
In the present paper, we based a search for candidates underlying different levels of salinity tolerance during germination in the Oregon Wolfe Barley mapping population (DOM ¥ REC) by proteomic profiling of the mature grain of lines showing differing levels of salinity tolerance. By contrasting the parents DOM and REC, displaying divergent stress responses, and two tolerant and two sensitive segregants, six protein spots were identified that showed a differential abundance between the tolerant and the sensitive lines. The tolerant lines expressed a higher level of 6-phosphogluconate dehydrogenase and glucose/ribitol dehydrogenase (Glc/RibDH). Both proteins were heterologously over-expressed in an osmo-sensitive yeast strain and over-expression of Glc/RibDH resulted in an enhanced ability of yeast transformants to grow on salt containing media. A quantitative trait locus (QTL) analysis of the population germinating at different salt concentrations led to the identification of two chromosome regions on 5H and one on 7H associated with salt stress response. A dense barley transcript map was employed to map the genomic region of all identified proteins. Two of these, heat-shock protein 70 and Glc/RibDH, co-localized with the identified QTL on chromosome 5H. The putative functional role of the candidates is discussed.
Aluminium (Al) toxicity is a major constraint to crop productivity in acidic soils. A quantitative trait locus (QTL) analysis was performed to identify the genetic basis of Al tolerance in the wheat cultivar 'Chinese Spring'. A nutrient solution culture approach was undertaken with the root tolerance index (RTI) and hematoxylin staining method as parameters to assess the Al tolerance. Using a set of D genome introgression lines, a major Al tolerance QTL was located on chromosome arm 4DL, explaining 31% of the phenotypic variance present in the population. A doubled haploid population was used to map a second major Al tolerance QTL to chromosome arm 3BL. This major QTL (Qalt CS .ipk-3B) in 'Chinese Spring' accounted for 49% of the phenotypic variation. Linkage of this latter QTL to SSR markers opens the possibility to apply marker-assisted selection (MAS) and pyramiding of this new QTL to improve the Al tolerance of wheat cultivars in breeding programmes.
Bread wheat Triticum aestivum L. possesses a genetic variation for the ability to survive and reproduce under salt stress conditions. Durum wheat (T. durum Desf.) is in general more sensitive in comparison to bread wheat, however, exceptions can be found showing the same extent of salt tolerance. Endemic wheats in general are characterised by a high adaptability to their environment. The level and variability of salt tolerance were assessed in a germplasm collection of 144 winter and spring wheat accessions from Georgia comprising Triticum aestivum L., T. durum Desf., T. dicoccon Schrank, T. polonicum L. and Georgian endemics: T. carthlicum Nevski, T. karamyschevii Nevski, T. macha Dekapr. et Menabde, T. timopheevii (Zhuk.) Zhuk. and T. zhukovskyi Menabde et Ericzjan. The accessions were tested for salt tolerance at the germination stage. Large variability in salt tolerance within the Georgian germplasm was found among the different wheat species. The endemic hexaploid winter wheat T. macha and the endemic tetraploid wheat T. timopheevii were among the most tolerant materials, thus presenting promising donors for salt tolerant traits in future breeding efforts for salinity tolerance in wheat.
Aegilops markgrafiiis a useful source of genes encoding both resistance to biotic stress and high seed lysine content. Bread wheat/Ae. markgrafiiintrogression lines expressing leaf rust resistance were developed from a cross between a leaf rust-resistantAe.markgrafiiaccession and the susceptible bread wheat cultivar ‘Alcedo’. The content of introgressed segments present in five sister introgression lines was assessed with the help of chromosome-specific simple sequence repeats (SSRs). One of the lines was used as a parent of a 140 individual F2mapping population, by crossing with the leaf rust-susceptible bread wheat cv. ‘Borenos’. The population was tested for susceptibility or resistance to leaf rust, and linkage analysis indicated the presence of a quantitative trait locus (QLr.ipk-2A) originating from theAe. markgrafiiparent, mapping to the distal segment of chromosome arm 2AS.
The pattern of inheritance of powdery mildew resistance expressed by two bread wheat (cultivar ‘Alcedo’)/Aegilops markgrafii introgression lines was explored using F2 populations bred from crosses made with the powdery mildew-susceptible cultivar ‘Kanzler’. Disease reaction was tested at both seedling and adult plant stages. Two resistance loci, designated QPm.ipk-1A and QPm.ipk-7A, were identified as mapping to the distal ends of chromosome arms 1AS and 7AL, respectively. Whereas QPm.ipk-1A was expressed throughout the plant's life, QPm.ipk-7A was only effective at the seedling stage. The map location of both resistance loci indicated that resistances originated from A. markgrafii. The possible genetic relationship of these disease-resistant genes to known Pm genes is discussed in the context of synteny.
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