Tsouris Andreas, Brach Gauthier, Friedrich Anne, Hou Jing, Schacherer Joseph
Université de Strasbourg, CNRS, GMGM UMR 7156, Strasbourg, France.
Institut Universitaire de France (IUF), Paris, France.
bioRxiv. 2023 Jul 25:2023.07.21.550015. doi: 10.1101/2023.07.21.550015.
Unraveling the genetic sources of gene expression variation is essential to better understand the origins of phenotypic diversity in natural populations. Genome-wide association studies identified thousands of variants involved in gene expression variation, however, variants detected only explain part of the heritability. In fact, variants such as low-frequency and structural variants (SVs) are poorly captured in association studies. To assess the impact of these variants on gene expression variation, we explored a half-diallel panel composed of 323 hybrids originated from pairwise crosses of 26 natural isolates. Using short- and long-read sequencing strategies, we established an exhaustive catalog of single nucleotide polymorphisms (SNPs) and SVs for this panel. Combining this dataset with the transcriptomes of all hybrids, we comprehensively mapped SNPs and SVs associated with gene expression variation. While SVs impact gene expression variation, SNPs exhibit a higher effect size with an overrepresentation of low-frequency variants compared to common ones. These results reinforce the importance of dissecting the heritability of complex traits with a comprehensive catalog of genetic variants at the population level.
揭示基因表达变异的遗传来源对于更好地理解自然种群中表型多样性的起源至关重要。全基因组关联研究确定了数千个参与基因表达变异的变体,然而,检测到的变体仅解释了部分遗传力。事实上,低频和结构变体(SVs)等变体在关联研究中捕获不足。为了评估这些变体对基因表达变异的影响,我们探索了一个半双列杂交群体,该群体由来自26个自然分离株两两杂交产生的323个杂种组成。使用短读长和长读长测序策略,我们为该群体建立了一个详尽的单核苷酸多态性(SNPs)和SVs目录。将该数据集与所有杂种的转录组相结合,我们全面绘制了与基因表达变异相关的SNPs和SVs。虽然SVs影响基因表达变异,但与常见变体相比,SNPs表现出更高的效应大小,且低频变体的比例过高。这些结果强化了在种群水平上用全面的遗传变体目录剖析复杂性状遗传力的重要性。