State Key Laboratory of Developmental Biology of Freshwater Fish, Hunan Normal University, Changsha, 410081, Hunan, China.
Key Laboratory of Tropical and Subtropical Fishery Resource Application and Cultivation of Ministry of Agriculture and Rural Affairs, Pearl River Fisheries Research Institute, Chinese Academy of Fishery Sciences, Guangzhou, 510380, Guangdong, China.
BMC Genomics. 2021 May 19;22(1):362. doi: 10.1186/s12864-021-07639-6.
Hybridization, which can quickly merge two or more divergent genomes and form new allopolyploids, is an important technique in fish genetic breeding. However, the merged subgenomes must adjust and coexist with one another in a single nucleus, which may cause subgenome interaction and dominance at the gene expression level and has been observed in some allopolyploid plants. In our previous studies, newly formed allodiploid hybrid fish derived from herbivorous Megalobrama amblycephala (♀) × carnivorous Culter alburnus (♂) had herbivorous characteristic. It is thus interesting to further characterize whether the subgenome interaction and dominance derive dietary adaptation of this hybrid fish.
Differential expression, homoeolog expression silencing and bias were investigated in the hybrid fish after 70 days of adaptation to carnivorous and herbivorous diets. A total of 2.65 × 10 clean reads (74.06 Gb) from the liver and intestinal transcriptomes were mapped to the two parent genomes based on specific SNPs. A total of 2538 and 4385 differentially expressed homoeologous genes (DEHs) were identified in the liver and intestinal tissues between the two groups of fish, respectively, and these DEHs were highly enriched in fat digestion and carbon metabolism, amino acid metabolism and steroid biosynthesis. Furthermore, subgenome dominance were observed in tissues, with paternal subgenome was more dominant than maternal subgenome. Moreover, subgenome expression dominance controlled functional pathways in metabolism, disease, cellular processes, environment and genetic information processing during the two dietary adaptation processes. In addition, few but sturdy villi in the intestine, significant fat accumulation and a higher concentration of malondialdehyde in the liver were observed in fish fed carnivorous diet compared with fish fed herbivorous diet.
Our results indicated that diet drives phenotypic and genetic variation, and the asymmetric expression of homoeologous genes (including differential expression, expression silencing and bias) may play key roles in dietary adaptation of hybrid fish. Subgenome expression dominance may contribute to uncovering the mechanistic basis of heterosis and also provide perspectives for fish genetic breeding and application.
杂交可以快速融合两个或多个不同的基因组,并形成新的异源多倍体,是鱼类遗传育种的重要技术。然而,合并的亚基因组必须在单个核内相互调整和共存,这可能导致基因表达水平的亚基因组相互作用和优势,在一些异源多倍体植物中已经观察到。在我们之前的研究中,从草食性团头鲂(♀)×肉食性翘嘴红鲌(♂)中衍生的新形成的异源二倍体杂交鱼具有草食性特征。因此,很有趣的是进一步描述这种杂交鱼的亚基因组相互作用和优势是否来自于饮食的适应。
在适应肉食性和草食性饮食 70 天后,研究了杂交鱼的差异表达、同系物表达沉默和偏倚。根据特定的 SNP,从肝脏和肠道转录组中总共获得了 2.65×10 个干净的读数(74.06Gb),并将其映射到两个亲本基因组上。在两组鱼的肝脏和肠道组织中,分别鉴定出 2538 个和 4385 个差异表达的同系物基因(DEHs),这些 DEHs 在脂肪消化和碳代谢、氨基酸代谢和类固醇生物合成中高度富集。此外,在组织中观察到亚基因组优势,父本亚基因组比母本亚基因组更占优势。此外,在两种饮食适应过程中,亚基因组表达优势控制着代谢、疾病、细胞过程、环境和遗传信息处理等功能途径。此外,与草食性饮食相比,肉食性饮食的鱼的肠道中绒毛较少但坚固,肝脏中脂肪积累显著,丙二醛浓度较高。
我们的结果表明,饮食驱动表型和遗传变异,同系物基因的不对称表达(包括差异表达、表达沉默和偏倚)可能在杂交鱼的饮食适应中发挥关键作用。亚基因组表达优势可能有助于揭示杂种优势的机制基础,也为鱼类遗传育种和应用提供了新的视角。