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通过分析野生二粒小麦 Gli-2 基因座区域揭示 α-醇溶蛋白基因家族的快速进化。

Rapid evolution of α-gliadin gene family revealed by analyzing Gli-2 locus regions of wild emmer wheat.

机构信息

United States Department of Agriculture-Agricultural Research Service USDA-ARS, Western Regional Research Center, 800 Buchanan Street, Albany, CA, 94710, USA.

Department of Plant Sciences, University of California, Davis, CA, 95616, USA.

出版信息

Funct Integr Genomics. 2019 Nov;19(6):993-1005. doi: 10.1007/s10142-019-00686-z. Epub 2019 Jun 13.

Abstract

α-Gliadins are a major group of gluten proteins in wheat flour that contribute to the end-use properties for food processing and contain major immunogenic epitopes that can cause serious health-related issues including celiac disease (CD). α-Gliadins are also the youngest group of gluten proteins and are encoded by a large gene family. The majority of the gene family members evolved independently in the A, B, and D genomes of different wheat species after their separation from a common ancestral species. To gain insights into the origin and evolution of these complex genes, the genomic regions of the Gli-2 loci encoding α-gliadins were characterized from the tetraploid wild emmer, a progenitor of hexaploid bread wheat that contributed the AABB genomes. Genomic sequences of Gli-2 locus regions for the wild emmer A and B genomes were first reconstructed using the genome sequence scaffolds along with optical genome maps. A total of 24 and 16 α-gliadin genes were identified for the A and B genome regions, respectively. α-Gliadin pseudogene frequencies of 86% for the A genome and 69% for the B genome were primarily caused by C to T substitutions in the highly abundant glutamine codons, resulting in the generation of premature stop codons. Comparison with the homologous regions from the hexaploid wheat cv. Chinese Spring indicated considerable sequence divergence of the two A genomes at the genomic level. In comparison, conserved regions between the two B genomes were identified that included α-gliadin pseudogenes containing shared nested TE insertions. Analyses of the genomic organization and phylogenetic tree reconstruction indicate that although orthologous gene pairs derived from speciation were present, large portions of α-gliadin genes were likely derived from differential gene duplications or deletions after the separation of the homologous wheat genomes ~ 0.5 MYA. The higher number of full-length intact α-gliadin genes in hexaploid wheat than that in wild emmer suggests that human selection through domestication might have an impact on α-gliadin evolution. Our study provides insights into the rapid and dynamic evolution of genomic regions harboring the α-gliadin genes in wheat.

摘要

α-醇溶蛋白是小麦粉中主要的面筋蛋白组之一,对面粉的加工性能有重要影响,同时包含主要的免疫原性表位,可导致严重的健康问题,包括乳糜泻(CD)。α-醇溶蛋白也是最年轻的面筋蛋白组,由一个大的基因家族编码。在不同小麦物种的 A、B 和 D 基因组中,该基因家族的大多数成员在与其共同祖先物种分离后,独立进化而来。为了深入了解这些复杂基因的起源和进化,我们从四倍体野生二粒小麦(六倍体面包小麦的祖先,提供了 AABB 基因组)中鉴定了编码α-醇溶蛋白的 Gli-2 基因座的基因组区域。首先使用基因组序列支架和光学基因组图谱重建了野生二粒小麦 A 和 B 基因组的 Gli-2 基因座区域的基因组序列。分别鉴定到 A 和 B 基因组区域的 24 个和 16 个α-醇溶蛋白基因。A 基因组和 B 基因组的α-醇溶蛋白假基因频率分别为 86%和 69%,主要是由于高度丰富的谷氨酰胺密码子中的 C 到 T 取代,导致提前出现终止密码子。与六倍体小麦 cv. Chinese Spring 的同源区域进行比较表明,在基因组水平上,两个 A 基因组的序列有相当大的差异。相比之下,两个 B 基因组之间鉴定到了保守区域,其中包括含有共享嵌套 TE 插入的α-醇溶蛋白假基因。基因组组织分析和系统发育树重建分析表明,尽管存在由物种形成产生的直系同源基因对,但大量的α-醇溶蛋白基因可能是在同源小麦基因组约 0.5 MYA 分离后,通过基因的重复或缺失产生的。六倍体小麦中完整的全长α-醇溶蛋白基因数量多于野生二粒小麦,这表明人类通过驯化选择可能对α-醇溶蛋白的进化产生影响。本研究为我们提供了在小麦中α-醇溶蛋白基因所在的基因组区域快速和动态进化的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b0bd/6797660/4fd4e5078405/10142_2019_686_Fig1_HTML.jpg

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