Kawaura Kanako, Miura Mayuko, Kamei Yoko, Ikeda Tatsuya M, Ogihara Yasunari
Kihara Institute for Biological Research, Yokohama City University.
Western Region Agricultural Research Center, National Agriculture and Food Research Organization.
Genes Genet Syst. 2018 Jul 13;93(1):9-20. doi: 10.1266/ggs.17-00034. Epub 2018 Jan 17.
The wheat seed storage proteins gliadin and glutenin are encoded by multigenes. Gliadins are further classified into α-, γ-, δ- and ω-gliadins. Genes encoding α-gliadins belong to a large multigene family, whose members are located on the homoeologous group 6 chromosomes at the Gli-2 loci. Genes encoding other gliadins are located on the homoeologous group 1 chromosomes at the Gli-1 loci. Two-dimensional polyacrylamide gel electrophoresis (2-DE) was used to characterize and profile the gliadins. The gliadins in aneuploid Chinese Spring wheat lines were then compared in this study. Gliadin proteins separated into 70 spots after 2-DE and a total of 10, 10 and 16 spots were encoded on chromosomes 6A, 6B and 6D, respectively, which suggested that they were α-gliadins. Similarly, six, three and seven spots were encoded on chromosomes 1A, 1B and 1D, respectively, which indicated that they were γ-gliadins. Spots that could not be assigned to chromosomes were N-terminally sequenced and were all determined to be α-gliadins or γ-gliadins. The 2-DE profiles showed that specific α-gliadin spots assigned to chromosome 6D were lost in tetrasomic chromosome 2A lines. Furthermore, western blotting against the Glia-α9 peptide, an epitope for celiac disease (CD), suggested that α-gliadins harboring the CD epitope on chromosome 6D were absent in the tetrasomic chromosome 2A lines. Systematic analysis of α-gliadins using 2-DE, quantitative RT-PCR and genomic PCR revealed that tetrasomic 2A lines carry deletion of a chromosome segment at the Gli-D2 locus. This structural alteration at the Gli-D2 locus may provide a genetic resource in breeding programs for the reduction of CD immunotoxicity.
小麦种子贮藏蛋白醇溶蛋白和谷蛋白由多基因编码。醇溶蛋白进一步分为α-、γ-、δ-和ω-醇溶蛋白。编码α-醇溶蛋白的基因属于一个大型多基因家族,其成员位于Gli-2位点的6号同源群染色体上。编码其他醇溶蛋白的基因位于Gli-1位点的1号同源群染色体上。采用二维聚丙烯酰胺凝胶电泳(2-DE)对醇溶蛋白进行表征和分析。本研究随后对非整倍体中国春小麦品系中的醇溶蛋白进行了比较。2-DE后醇溶蛋白分离为70个斑点,其中分别有10、10和16个斑点在6A、6B和6D染色体上编码,这表明它们是α-醇溶蛋白。同样,分别有6、3和7个斑点在1A、1B和1D染色体上编码,这表明它们是γ-醇溶蛋白。无法定位到染色体上的斑点进行了N端测序,结果均确定为α-醇溶蛋白或γ-醇溶蛋白。2-DE图谱显示,在四体2A品系中,位于6D染色体上的特定α-醇溶蛋白斑点缺失。此外,针对麸质过敏性肠病(CD)的表位Glia-α9肽的蛋白质免疫印迹分析表明,四体2A品系中6D染色体上含有CD表位的α-醇溶蛋白缺失。利用2-DE、定量逆转录聚合酶链反应(RT-PCR)和基因组聚合酶链反应(PCR)对α-醇溶蛋白进行系统分析,结果表明四体2A品系在Gli-D2位点存在一个染色体片段缺失。Gli-D2位点的这种结构改变可能为育种计划中降低CD免疫毒性提供一种遗传资源。