Mutants at gliadin loci on the basis of the common wheat cultivar Bezostaya 1

Aim. The aim of this study was to isolate and propagate mutants at gliadin loci developed on the basis of the common wheat cultivar Bezostaya 1. Methods. We searched for spontaneous and gamma-irradiation induced mutations at gliadin loci among the progeny of F1 and F2 plants from crosses between near-isogenic lines by gliadin loci on the basis of the cultivar Bezostaya 1, including lines with the wheat-rye 1BL.1RS translocation. To identify mutations, we performed acid polyacrylamide gel electrophoresis and SDS-electrophoresis of storage proteins. Results. On the basis of the common wheat cultivar Bezostaya 1, five mutants (six mutations) at gliadin loci were isolated and propagated, four of which were described for the first time. Three mutations occurred at the Gli-R1 locus involved in the wheat-rye 1BL.1RS translocation (the loss of secalins, intensification of a secalin component, and increased mobility of a secalin component). Two mutations were identified in the allele Gli-B1b, one caused the null-allele at the Gli-A2 locus. Conclusions. The material of mutants is of importance for studying the role of certain groups of storage proteins and their components in quality determination, as well as mechanisms of regulation of storage protein synthesis. Keywords: Triticum aestivum, gliadin, secalin, mutation, 1BL.1RS translocation.

Sequence elimination in hybrid offspring of wheat-Agropyron cristatum (L.) Gaertn introgression line Pubing3504 × common wheat cultivar Jing4839

ABSTRACTSequence elimination is one of main reasons for homologous chromosome differentiation in common wheat. Sequence elimination can occur in genome-specific sequences, chromosome-specific sequences, and repeat sequences in the wheat genome. Genetic polymorphism loci in chromosome-specific sequences can be used to develop molecular markers including simple sequence repeats (SSRs), insertions and deletions, and single nucleotide polymorphisms (SNPs). Pubing3504 is a wheat-Agropyron cristatum (L.) Gaertn introgression line, and Jing4839 is a common wheat cultivar. Assessment of their recombinant inbred line (RIL) population using 120 pairs of SSR markers covering all wheat chromosomes indicated that sequence elimination occurred at the short arm of chromosome 1A (1AS). We developed 13 pairs of new co-dominant SSR markers and constructed a genetic linkage map of 1AS; we found that the segment with sequence elimination is from SSR110 to the end of 1AS. We further developed 10 pairs of dominant SNP markers of Pubing3504, 10 pairs of dominant SNP markers of Jing4839, and 10 pairs of primers designed in SNP flanking sequences to assess RILs. We found that all chromosome segments with sequence elimination came from Jing4839. The sequence elimination occurred in SSR loci, SNP loci, and coding sequences. There was no homologous recombination in the chromosome segment with sequence elimination. We suggest that sequence elimination causes the differentiation of chromosomes and the chromosome differentiation affects the homologous pairing at the chromosome segment in meiosis, which further affects the occurrence of homologous recombination at the chromosome segment.