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

IF 4.4 1区 生物学 Q1 BIOLOGY
Robert Mukiibi, Serena Ferraresso, Rafaella Franch, Luca Peruzza, Giulia Dalla Rovere, Massimiliano Babbucci, Daniela Bertotto, Anna Toffan, Francesco Pascoli, Sara Faggion, Carolina Peñaloza, Costas S Tsigenopoulos, Ross D Houston, Luca Bargelloni, Diego Robledo
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引用次数: 0

Abstract

Background: Viral nervous necrosis (VNN) is an important viral disease threatening global aquaculture sustainability and affecting over 50 farmed and ecologically important fish species. A major QTL for resistance to VNN has been previously detected in European sea bass, but the underlying causal gene(s) and mutation(s) remain unknown. To identify the mechanisms and genetic factors underpinning resistance to VNN in European sea bass, we employed integrative analyses of multiple functional genomics assays in European sea bass.

Results: The estimated heritability of VNN resistance was high (h2 ~ 0.40), and a major QTL explaining up to 38% of the genetic variance of the trait was confirmed on chromosome 3, with individuals with the resistant QTL genotype showing a 90% survivability against a VNN outbreak. Whole-genome resequencing analyses narrowed the location of this QTL 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 CHR3:10,077,301, exhibited higher frequencies (0.55 to 0.77) in Eastern Mediterranean Sea bass populations, which show considerably higher levels of resistance to VNN, as compared to susceptible West Mediterranean and Atlantic populations (0.15-0.25).

Conclusions: The SNP variant CHR3:10,077,301, 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 in fish 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.

综合功能基因组分析确定了欧洲海鲈鱼抗病主要QTL的调控变异。
背景:病毒性神经坏死(VNN)是一种重要的病毒性疾病,威胁着全球水产养殖的可持续性,影响着50多种具有重要生态意义的养殖鱼类。以前在欧洲鲈鱼中发现了一个主要的VNN抗性QTL,但潜在的致病基因和突变仍然未知。为了确定欧洲黑鲈对VNN抗性的机制和遗传因素,我们对欧洲黑鲈进行了多种功能基因组学分析。结果:VNN抗性的估计遗传力较高(h2 ~ 0.40),在第3染色体上确认了一个解释该性状遗传变异38%的主要QTL,具有抗性QTL基因型的个体对VNN爆发的存活率为90%。全基因组重测序分析将该QTL的定位缩小到一个小区域,该区域包含4个拷贝的干扰素α诱导蛋白27-like 2A (IFI27L2A)基因和1个拷贝的干扰素α诱导蛋白27-like 2 (IFI27L2)基因。RNA测序显示,QTL基因型与两个IFI27L2A基因和IFI27L2基因的表达有明显的关联。结合染色质可及性和组蛋白修饰数据,确定了其中两个基因(IFI27L2A和IFI27L2)活性调控区域的两个snp,并预测了抗性等位基因的转录因子结合位点增益。这些等位基因,特别是SNP变异CHR3:10,077,301,在东地中海鲈鱼种群中显示出更高的频率(0.55至0.77),与易感的西地中海和大西洋种群(0.15-0.25)相比,对VNN的抗性水平要高得多。结论:通过调节IFI27L2和IFI27L2A基因,SNP变异CHR3:10,077,301可能是欧洲黑鲈对VNN抗性的致病突变。这是首次发现的鱼类抗病性状的致病突变之一,为标记辅助选择和生物技术方法增强欧洲黑鲈和其他易感物种对VNN的抗性铺平了道路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
BMC Biology
BMC Biology 生物-生物学
CiteScore
7.80
自引率
1.90%
发文量
260
审稿时长
3 months
期刊介绍: BMC Biology is a broad scope journal covering all areas of biology. Our content includes research articles, new methods and tools. BMC Biology also publishes reviews, Q&A, and commentaries.
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