DNA Methylation and Subgenome Dominance Reveal the Role of Lipid Metabolism in Jinhu Grouper Heterosis

Author:

Liu Yang123ORCID,Wang Linna123ORCID,Li Zhentong123,Li Linlin123,Chen Shuai1,Duan Pengfei1,Wang Xinyi1,Qiu Yishu1,Ding Xiaoyu1,Su Jinzhi1,Deng Yuan1,Tian Yongsheng123ORCID

Affiliation:

1. State Key Laboratory of Mariculture Biobreeding and Sustainable Goods, Yellow Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, Qingdao 266071, China

2. Laboratory for Marine Fisheries Science and Food Production Processes, Qingdao Marine Science and Technology Center, Qingdao 266237, China

3. Hainan Innovation Research Institute, Chinese Academy of Fishery Sciences, Sanya 572000, China

Abstract

Heterosis of growth traits in economic fish has benefited the production of aquaculture for many years, yet its genetic and molecular basis has remained obscure. Nowadays, a new germplasm of hybrid Jinhu grouper (Epinephelus fuscoguttatus ♀ × E. tukula ♂), abbreviated as EFT, exhibiting paternal-biased growth heterosis, has provided an excellent model for investigating the potential regulatory mechanisms of heterosis. We integrated transcriptome and methylome to unravel the changes of gene expression, epigenetic modification, and subgenome dominance in EFT compared with maternal E. fuscoguttatus. Integration analyses showed that the heterotic hybrids showed lower genomic DNA methylation levels than the purebred parent, and the up-regulated genes were mostly DNA hypomethylation. Furthermore, allele-specific expression (ASE) detected paternal subgenome dominance-regulated paternal-biased heterosis, and paternal bias differentially expressed genes (DEGs) were wholly up-regulated in the muscle. Multi-omics results highlighted the role of lipid metabolism, particularly “Fatty acid synthesis”, “EPA biosynthesis”, and “Signaling lipids”, in EFT heterosis formation. Coherently, our studies have proved that the eicosapentaenoic acid (EPA) of EFT was greater than that of maternal E. fuscoguttatus (8.46% vs. 7.46%). Finally, we constructed a potential regulatory network for control of the heterosis formation in EFT. Among them, fasn, pparg, dgat1, igf1, pomca, fgf8a, and fgfr4 were identified as key genes. Our results provide new and valuable clues for understanding paternal-biased growth heterosis in EFT, taking a significant step towards the molecular basis of heterosis.

Funder

Key Research and Development Project of Hainan Province

National Key Research and Development Program of China

Taishan Industry Leading talent Project

Key Research and Development Project of Shangdong Province

China Agriculture Research System of MOF and MARA

Qingdao Natural Science Foundation

Qingdao Science and Technology Benefiting the People Demonstration Project

Central Public-Interest Scientific Institute Basal Research Fund, CAFS

Yellow Sea Fisheries Research Institute Research Fees

Qingdao Postdoctoral Applied Research Project

Publisher

MDPI AG

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