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Synthetic recombination form RS7 (BBAAUS), in which the first two genomes, A and B, originate from common wheat, and the third recombinant genome consists of Aegilops speltoides (S) and Ae. umbellulata (U) chromosomes, was obtained from crossing synthetic forms Avrodes (BBAASS) and Avrolata (BBAAUU). Resistant to leaf rust, yellow rust and powdery mildew, introgression lines have been obtained from backcrosses with the susceptible varieties of common wheat Krasnodarskaya 99, Fisht and Rostislav. PCR analysis showed the presence of amplification fragments with marker SCS421 specific for the Lr28 gene in the line 4991n17. The cytological study (С-banding and FISH) of 14 lines has revealed chromosomal modifications in 12 of them. In most cases, the lines carry translocations from Ae. speltoides, which were identified in chromosomes 1D, 2D, 3D, 2B, 4B, 5B and 7B. Also, lines with the substituted chromosomes 1S (1B), 4D (4S), 5D (5S) and 7D (7S) were identified. Lines that have genetic material from Ae. speltoides and Ae umbellulata at once were revealed. In the line 3379n14, translocations in the short arm of chromosome 7D from Ae. umbellulata and chromosomes 5BL, 1DL, 2DL from Ae. speltoides were revealed. The line 4626p16 presumably has a translocation on the long arm of chromosome 2D from Ae. umbellulata and the T7SS.7SL-7DL translocation from Ae. speltoides. The T1DS.1DL-1SL and T3DS.3DL-3SL translocations from Ae. speltoides, and T2DS.2DL-2UL and T7DL.7DS-7US from Ae. umbellulata have been obtained for the first time. These lines may carry previously unidentified disease resistance genes and, in particular, leaf rust resistance genes from Ae. speltoides and Ae. umbellulata.

Using chromosome C-banding and electrophoresis of grain storage proteins, gliadins, 17 Triticum aestivumAegilops columnaris lines with substitutions of chromosomes of homoeologous groups 1 and 6 were examined. Based on their high polymorphism, gliadins were used to identify alien genetic material. For all of the lines examined, electrophoretic analysis of gliadin spectra confirmed substitution of wheat chromosomes 6A, 6D or 1D for the homoeologous Aegilops chromosomes of genomes Uс or Xс. The substitution manifested in the disappearance of the products of gliadin-coding genes on chromosomes 6A, 6D or 1D with the simultaneous appearance of the products of genes localized on alien chromosomes of genomes Uс or Xс. Thus, Aegilops chromosomes were shown to be functionally active in the alien wheat genome. The absence of alien genes expression in the lines carrying a long arm deletion in chromosome 6X c suggested that the gliadin-coding locus moved from the short chromosome arm (its characteristic position in all known wheat species) to the long one. This is probably associated with a large species-specific pericentric inversion. In spite of losing a part of its long arm and combination with a non-homologous chromosome of a different genome (4BL), chromosome 1D was fully functioning. For Aegilops , the block type of gliadin components inheritance was shown, indicating similarity in the structural organization of gliadin-coding loci in these genera. Based on determining genetic control of various polypeptides in the electrophoretic aegilops spectrum, markers to identify Ae. columnaris chromosomes 1Xс, 6Xс and 6Uс were constructed.

Aegilops columnaris Zhuk. is a potential source of new genes for wheat improvement. However, this species has not yet been used in practical breeding. In the present work we have for the first time reported the development and molecular-cytogenetic characterization of T. aestivum×Ae. columnaris introgression lines. Analysis has not revealed alien genetic material in five of the 20 lines we have studied, while the remaining lines carried from 1 to 3 pairs of Aegilops chromosomes as addition(s) or substitution(s) to wheat chromosomes. Altogether, five different chromosomes of Aegilops columnaris have been detected in the karyotypes of 15 lines by C-banding and fluorescent in-situ hybridization (FISH). Based on substitution spectra, these chromosomes were identified as 3Ае1, 3Ае2, 5Ае2, 6Ае1 and 6Ае2. In addition, another Aegilops chromosome has been found in the line 2305/1 as a monosomic addition; due to the lack of group-specific markers we were unable to assign this chromosome to a particular genome or a genetic group and therefore it was designated Ае-а. In several lines acrocentric and telocentric chromosomes have been revealed (Ae-b and Ae-c). It is most likely that these chromosomes were derived from unknown Aegilops chromosomes due to a large deletion. A comparison of electrophoretic spectra of gliadins in introgression lines L-2310/1 and L-2304/1 with substitutions of chromosome 6D with two different chromosomes of Ae. columnaris (these lines were assigned to the 6th homoeologous group based on C-banding data) has shown that they carry different alleles of the gliadin loci. This observation confirmed that lines L-2310/1 and L-2304/1 contained non-identical 6Ae chromosomes. Taking into consideration our previous results of FISH analyses, three other Ae. columnaris chromosomes can be assigned to homoeologous groups 1, 5 and 7 of the U-genome based on the location of 5S and 45S rDNA loci (1U and 5U) or pSc119.2 probe distribution (7U). Thus, based on our current data as well as on the results of earlier work, we can identify eight out of the 14 chromosomes of Aegilops columnaris.