Université de Strasbourg, CNRS, Génétique Moléculaire, Génomique et Microbiologie UMR 7156, Strasbourg, 67000, France.
Institut Universitaire de France, Paris, 67000, France.
Proc Natl Acad Sci U S A. 2022 Sep 13;119(37):e2204206119. doi: 10.1073/pnas.2204206119. Epub 2022 Sep 6.
In natural populations, the same mutation can lead to different phenotypic outcomes due to the genetic variation that exists among individuals. Such genetic background effects are commonly observed, including in the context of many human diseases. However, systematic characterization of these effects at the species level is still lacking to date. Here, we sought to comprehensively survey background-dependent traits associated with gene loss-of-function (LoF) mutations in 39 natural isolates of using a transposon saturation strategy. By analyzing the modeled fitness variability of a total of 4,469 genes, we found that 15% of them, when impacted by a LoF mutation, exhibited a significant gain- or loss-of-fitness phenotype in certain natural isolates compared with the reference strain S288C. Out of these 632 genes with predicted background-dependent fitness effects, around 2/3 impact multiple backgrounds with a gradient of predicted fitness change while 1/3 are specific to a single genetic background. Genes related to mitochondrial function are significantly overrepresented in the set of genes showing a continuous variation and display a potential functional rewiring with other genes involved in transcription and chromatin remodeling as well as in nuclear-cytoplasmic transport. Such rewiring effects are likely modulated by both the genetic background and the environment. While background-specific cases are rare and span diverse cellular processes, they can be functionally related at the individual level. All genes with background-dependent fitness effects tend to have an intermediate connectivity in the global genetic interaction network and have shown relaxed selection pressure at the population level, highlighting their potential evolutionary characteristics.
在自然种群中,由于个体之间存在遗传变异,相同的突变可能导致不同的表型结果。这种遗传背景效应很常见,包括在许多人类疾病的背景下。然而,迄今为止,在物种水平上系统地表征这些效应仍然缺乏。在这里,我们试图使用转座子饱和策略全面调查与 39 个自然分离株中基因功能丧失(LoF)突变相关的背景依赖性特征。通过分析总共 4469 个基因的模型适应性变异性,我们发现其中 15%的基因在受到 LoF 突变的影响时,与参考菌株 S288C 相比,在某些自然分离株中表现出显著的适应性增益或损失表型。在这 632 个具有预测背景依赖性适应性效应的基因中,大约 2/3 影响多个背景,具有预测适应性变化的梯度,而 1/3 是特定于单个遗传背景的。与线粒体功能相关的基因在表现出连续变化的基因集中显著过表达,并显示出与涉及转录和染色质重塑以及核细胞质运输的其他基因的潜在功能重连。这种重连效应可能受到遗传背景和环境的调节。虽然背景特异性的情况很少见,涵盖了多种细胞过程,但它们在个体水平上可能具有功能相关性。所有具有背景依赖性适应性效应的基因在全局遗传相互作用网络中倾向于具有中等连接性,并在群体水平上显示出松弛的选择压力,突出了它们的潜在进化特征。