Integrated functional genomic analysis identifies the regulatory variants underlying a major QTL for disease resistance in European sea bass

Mukiibi, R.; Ferraresso, S.; Franch, R.; Peruzza, L.; Rovere, G. D.; Babbucci, M.; Bertotto, D.; Toffan, A.; Pascoli, F.; Faggion, S.; Penaloza, C.; Tsigenopoulos, C. S.; Houston, R. D.; Bargelloni, L.; Robledo, D.

doi:10.1101/2024.07.06.602346

bioRxiv · 10.1101/2024.07.06.602346

Integrated functional genomic analysis identifies the regulatory variants underlying a major QTL for disease resistance in European sea bass

Mukiibi, R.·Ferraresso, S.·Franch, R.·Peruzza, L.·Rovere, G. D.·Babbucci, M.·Bertotto, D.·Toffan, A.·Pascoli, F.·Faggion, S.·Penaloza, C.·Tsigenopoulos, C. S.·Houston, R. D.·Bargelloni, L.·Robledo, D.

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Abstract

BackgroundViral nervous necrosis (VNN) is a viral disease threatening the sustainability of global aquaculture, and affecting over 50 of farmed and ecologically important species. A major QTL for resistance to VNN has been previously described in European sea bass, but the underlying causal gene(s) and mutation(s) are unknown. To identify the mechanisms and genetic factors underpinning resistance to VNN, we integrated farmed and wild genetic data with multiple functional genomics assays in a farmed European sea bass population. ResultsA high heritability (h2 [~] 0.40) was estimated for VNN resistance. A major QTL for this trait was confirmed on chromosome 3, and whole-genome resequencing narrowed its location to a small region containing 4 copies of interferon alpha inducible protein 27-like 2A (IFI27L2A) genes, and one copy of the interferon alpha inducible protein 27-like 2 (IFI27L2) gene. RNA sequencing revealed a clear association between the QTL genotype and the expression of two of the IFI27L2A genes, and the IFI27L2 gene. Integration with chromatin accessibility and histone modification data pinpointed two SNPs in active regulatory regions of two of these genes (IFI27L2A and IFI27L2), and transcription factor binding site gains for the resistant alleles were predicted. These alleles, particularly the SNP variant CHR3:10077301, exhibited higher frequency in Eastern Mediterranean sea bass populations, which show considerably higher levels of resistance to VNN. ConclusionsThe SNP variant CHR3:10077301, through modulation of IFI27L2 and IFI27L2A genes, is likely the causative mutation underlying resistance to VNN in European sea bass. This is one of the first causative mutations discovered for disease resistance traits, and paves the way for marker-assisted selection as well as biotechnological approaches to enhance resistance to VNN in European sea bass and other susceptible species.

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Mukiibi, R., Ferraresso, S., Franch, R., Peruzza, L., Rovere, G. D., Babbucci, M., Bertotto, D., Toffan, A., Pascoli, F., Faggion, S., Penaloza, C., Tsigenopoulos, C. S., Houston, R. D., Bargelloni, L., Robledo, D.. 2024-07-10. Integrated functional genomic analysis identifies the regulatory variants underlying a major QTL for disease resistance in European sea bass. https://doi.org/10.1101/2024.07.06.602346

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