Genomics and Gene Discovery Research Unit, Western Regional Research Center, Agricultural Research Service, United States Department of Agriculture, Albany, CA, USA.
PLoS One. 2012;7(12):e52139. doi: 10.1371/journal.pone.0052139. Epub 2012 Dec 20.
The utility of mining DNA sequence data to understand the structure and expression of cereal prolamin genes is demonstrated by the identification of a new class of wheat prolamins. This previously unrecognized wheat prolamin class, given the name δ-gliadins, is the most direct ortholog of barley γ3-hordeins. Phylogenetic analysis shows that the orthologous δ-gliadins and γ3-hordeins form a distinct prolamin branch that existed separate from the γ-gliadins and γ-hordeins in an ancestral Triticeae prior to the branching of wheat and barley. The expressed δ-gliadins are encoded by a single gene in each of the hexaploid wheat genomes. This single δ-gliadin/γ3-hordein ortholog may be a general feature of the Triticeae tribe since examination of ESTs from three barley cultivars also confirms a single γ3-hordein gene. Analysis of ESTs and cDNAs shows that the genes are expressed in at least five hexaploid wheat cultivars in addition to diploids Triticum monococcum and Aegilops tauschii. The latter two sequences also allow assignment of the δ-gliadin genes to the A and D genomes, respectively, with the third sequence type assumed to be from the B genome. Two wheat cultivars for which there are sufficient ESTs show different patterns of expression, i.e., with cv Chinese Spring expressing the genes from the A and B genomes, while cv Recital has ESTs from the A and D genomes. Genomic sequences of Chinese Spring show that the D genome gene is inactivated by tandem premature stop codons. A fourth δ-gliadin sequence occurs in the D genome of both Chinese Spring and Ae. tauschii, but no ESTs match this sequence and limited genomic sequences indicates a pseudogene containing frame shifts and premature stop codons. Sequencing of BACs covering a 3 Mb region from Ae. tauschii locates the δ-gliadin gene to the complex Gli-1 plus Glu-3 region on chromosome 1.
利用 DNA 序列数据来了解谷物醇溶蛋白基因的结构和表达的效用,通过鉴定一种新的小麦醇溶蛋白类得以体现。这个以前未被识别的小麦醇溶蛋白类,被命名为δ-麦谷蛋白,是大麦γ3-麦醇溶蛋白最直接的同源物。系统发育分析表明,同源的 δ-麦谷蛋白和γ3-麦醇溶蛋白形成一个独特的醇溶蛋白分支,在小麦和大麦分支之前,在一个祖先的小麦族中,与γ-麦谷蛋白和γ-麦醇溶蛋白分开存在。在六倍体小麦基因组中的每一个中,表达的 δ-麦谷蛋白由一个单一的基因编码。这个单一的 δ-麦谷蛋白/γ3-麦醇溶蛋白的同源物可能是小麦族的一个普遍特征,因为对三个大麦品种的 EST 检查也证实了一个单一的 γ3-麦醇溶蛋白基因。EST 和 cDNA 的分析表明,这些基因除了二倍体 Triticum monococcum 和 Ae. tauschii 之外,在至少五个六倍体小麦品种中表达。后两个序列还允许将 δ-麦谷蛋白基因分别分配到 A 和 D 基因组,第三个序列类型假定来自 B 基因组。对于有足够 EST 的两个小麦品种,表达模式不同,即 cv Chinese Spring 从 A 和 B 基因组表达基因,而 cv Recital 从 A 和 D 基因组具有 EST。Chinese Spring 的基因组序列表明,D 基因组基因由于串联过早终止密码子而失活。第四个 δ-麦谷蛋白序列发生在 Chinese Spring 和 Ae. tauschii 的 D 基因组中,但没有 EST 与该序列匹配,并且有限的基因组序列表明含有移码和过早终止密码子的假基因。从 Ae. tauschii 覆盖 3 Mb 区域的 BAC 测序将 δ-麦谷蛋白基因定位到染色体 1 上的复杂 Gli-1 加 Glu-3 区域。