The generation of stop codons in the coding sequences resulted mainly from single-base transitions, with selleck the C to T change predominating and accounting for about 70% of these [8] and [13]. Additionally, and consistent with recent studies [29] and [30] of other wheat genomic regions, it has been shown that α-gliadin genes in the Gli-2 regions are not evenly distributed, but are clustered mainly into numerous small gene islands separated by large blocks of repetitive elements, especially retrotransposons, which are abundant (accounting

for about 70% of the sequences) in these regions [7]. Thus, it has been suggested that retrotransposons contribute to the dynamic changes in these regions, including frequent gene duplications and insertions, as well as illegitimate recombination, which appears to have a major

impact on increasing the number of genes [7], [29] and [30]. The extremely high copy numbers of α-gliadin not only make it more difficult to purify a single component from a compound of related proteins, but make it more complicated to elucidate the expression and function of individual genes [31]. Heterologous expression has frequently been used to produce single pure components for studying http://www.selleckchem.com/products/byl719.html structure–function relationships of proteins in vitro. However, heterologous expression of a protein with stable disulfide bonds in E. coli inevitably results in the formation of an inclusion-body protein, and Levetiracetam the protein yield depends largely on the type of expressed gene. So the high-level expression of α-gliadins in vitro is still difficult [32] and [33], meaning that the study of structure–function relationships of single α-gliadin genes by heterologous expression, purification, and functional analysis in vitro is very limited [10]. In the present study, using a pair of degenerate primers that represent the majority of full-ORF α-gliadin genes in GenBank, 43 unique clones from Zhengmai 004 were obtained by

comparative analysis among a total of 85 positive clones. NCBI BLAST searching of each sequence showed that 42 of them had 84%–99% identity with sequences in GenBank (except for Z4A-22 with 100% identity with JX828270, which we had previously cloned from common wheat cultivar Zhengmai 9023), suggesting that they are new members of α-gliadin gene family. In addition, consistent with previous findings, about 49% of the clones are pseudogenes, 81% of which resulted from single-base transitions, especially the C to T change that accounted for 91% of these. Of the 22 full-ORF genes, one (Z4A-15) lacked the second conserved cysteine residue in the unique domain I, while four genes (Z4A-7, Z4A-14, Z4A-17 and Z4A-20) contained an extra cysteine residue in the C-terminal unique domain II.