Takahagi Kotaro, Inoue Komaki, Mochida Keiichi
Bioproductivity Informatics Research Team, RIKEN Center for Sustainable Resource Science, Yokohama, Japan.
Graduate School of Nanobioscience, Yokohama City University, Yokohama, Japan.
Front Plant Sci. 2018 Aug 8;9:1163. doi: 10.3389/fpls.2018.01163. eCollection 2018.
Genome duplications aid in the formation of novel molecular networks through regulatory differentiation of the duplicated genes and facilitate adaptation to environmental change. Hexaploid wheat, , contains three homoeologous chromosome sets, the A-, B-, and D-subgenomes, which evolved through interspecific hybridization and subsequent whole-genome duplication. The divergent expression patterns of the homoeologs in hexaploid wheat suggest that they have undergone transcriptional and/or functional differentiation during wheat evolution. However, the distribution of transcriptionally differentiated homoeologs in gene regulatory networks and their related biological functions in hexaploid wheat are still largely unexplored. Therefore, we retrieved 727 publicly available wheat RNA-sequencing (RNA-seq) datasets from various tissues, developmental stages, and conditions, and identified 10,415 expressed homoeologous triplets. Examining the co-expression modules in the wheat transcriptome, we found that 66% of the expressed homoeologous triplets possess all three homoeologs grouped in the same co-expression modules. Among these, 15 triplets contain co-expressed homoeologs with differential expression levels between homoeoalleles across ≥ 95% of the 727 RNA-seq datasets, suggesting a consistent trend of homoeolog expression bias. In addition, we identified 2,831 differentiated homoeologs that showed gene expression patterns that deviated from those of the other two homoeologs. We found that seven co-expression modules contained a high proportion of such differentiated homoeologs, which accounted for ≥ 20% of the genes in each module. We also found that five of the co-expression modules are abundantly composed of genes involved in biological processes such as chloroplast biogenesis, RNA metabolism, putative defense response, putative posttranscriptional modification, and lipid metabolism, thereby suggesting that, the differentiated homoeologs might highly contribute to these biological functions in the gene network of hexaploid wheat.
基因组复制通过复制基因的调控分化有助于形成新的分子网络,并促进对环境变化的适应。六倍体小麦含有三个同源染色体组,即A、B和D亚基因组,它们通过种间杂交和随后的全基因组复制进化而来。六倍体小麦中同源基因的不同表达模式表明它们在小麦进化过程中经历了转录和/或功能分化。然而,转录分化的同源基因在基因调控网络中的分布及其在六倍体小麦中的相关生物学功能仍 largely unexplored。因此,我们从各种组织、发育阶段和条件中检索了727个公开可用的小麦RNA测序(RNA-seq)数据集,并鉴定出10415个表达的同源三联体。通过检查小麦转录组中的共表达模块,我们发现66%的表达同源三联体的所有三个同源基因都聚集在同一个共表达模块中。其中,15个三联体包含共表达的同源基因,其同源等位基因之间的表达水平差异在727个RNA-seq数据集中的≥95%,表明同源基因表达偏向存在一致趋势。此外,我们鉴定出2831个分化的同源基因,其基因表达模式与其他两个同源基因不同。我们发现七个共表达模块包含高比例的此类分化同源基因,每个模块中此类基因占≥20%。我们还发现,五个共表达模块大量由参与叶绿体生物发生、RNA代谢、假定的防御反应、假定的转录后修饰和脂质代谢等生物学过程的基因组成,从而表明,分化的同源基因可能对六倍体小麦基因网络中的这些生物学功能有很大贡献。