Abstract

Heterosis is a complex biological phenomenon in which hybridization produces offspring that exhibit superior phenotypic characteristics compared with the parents. Heterosis is widely utilized in agriculture, for example in fish farming; however, its underlying molecular basis remains elusive. To gain a comprehensive and unbiased molecular understanding of fish heterosis, we analyzed the mRNA, miRNA, and proteomes of the livers of three catfish species, Pelteobagrus fulvidraco, P. vachelli, and their hybrid, the hybrid yellow catfish "Huangyou-1" (P. fulvidraco ♀ × P. vachelli ♂). Using next-generation sequencing and mass spectrometry, we show that the nonadditive, homoeolog expression bias and expression level dominance pattern were readily identified at the transcriptional, post-transcriptional, or protein levels, providing the evidence for the widespread presence of dominant models during hybridization. A number of predicted miRNA-mRNA-protein pairs were found and validated by qRT-PCR and PRM assays. Furthermore, several diverse key pathways were identified, including immune defense, metabolism, digestion and absorption, and cell proliferation and development, suggesting the vital mechanisms involved in the generation of the heterosis phenotype in progenies. We propose that the high parental expression of genes/proteins (growth, nutrition, feeding, and disease resistance) coupled with low parental miRNAs of the offspring, are inherited from the mother or father, thus indicating that the offspring were enriched with the advantages of the father or mother. We provide new and important information about the molecular mechanisms of heterosis, which represents a significant step toward a more complete elucidation of this phenomenon.

Highlights

  • Vital Genetic Pattern of Homoeolog Expression Bias (HEB) in Hybrid F1—To address whether the observed category of HEB truly reflects the homoeolog expression bias in the hybrid yellow catfish Huangyou-1, we compared the parental diploids and diploid hybrids of 11,789 homologous genes with homoeolog-specific SNPs on a case-by-case basis

  • To further support ELD and the nonadditive mechanism for H heterosis, we found that these significant KEGG terms enriched from ELD-F/M genes/proteins were related to similar biological processes with NEG/nonadditively expressed proteins (NEP), such as immune defense, metabolism, digestion and absorption, and cell proliferation and development (Figs. 2, 4, and 5)

  • We propose that the high parental expression of genes/proteins coupled with low parental miRNAs of the offspring are inherited from the mother or father, indicating that the offspring were enriched with the advantages of the father or mother and thereby obtained heterosis

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Summary

Graphical Abstract

In Brief mRNA-seq, miRNA-seq, proteomes of P. fulvidraco, P. vachelli, the hybrid Huangyou-1 livers were characterized. Yellow catfish Huangyou-1 (hybrid F1, H), produced from the hybridization of Pelteobagrus fulvidraco & (female, F) ϫ P. vachelli ( (male, M), has advantages such as a seductive body color, faster growth and development, a high feeding rate, and greater immunity when compared with its parents [35] These special characteristics of H suggest that it is a significant aquaculture species and a potential model organism for study of the molecular mechanisms of heterosis. The present NGST and Tandem Mass Tags (TMT) study should provide unprecedented resources to address such questions as to how hybridization affects gene/protein expression and changes the molecular pathways, which could lead to broader adaptability in nascent hybrid fish, and whether miRNAs participate in this process For this purpose, we performed mRNA-seq, miRNA-seq, and proteomics in liver from H, F, and M (Fig. 1), which is the first report on the integrated analysis of fishes and offers deeper insight into heterosis miRNA-mRNA-protein pairs, validated by qRTPCR and parallel reaction monitoring (PRM) assays [38]. Our data suggest a potential miRNA moderated regulatory mechanism for gene expression as well as protein expression as the basis for heterosis phenotypes in hybridization

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