Birolo Giovanni, Benevenuta Silvia, Fariselli Piero, Capriotti Emidio, Giorgio Elisa, Sanavia Tiziana
Department of Medical Sciences, University of Torino, Italy.
Department of Pharmacy and Biotechnology (FaBiT), University of Bologna, Italy.
Front Mol Biosci. 2021 Feb 1;8:620793. doi: 10.3389/fmolb.2021.620793. eCollection 2021.
Missense variants are among the most studied genome modifications as disease biomarkers. It has been shown that the "perturbation" of the protein stability upon a missense variant (in terms of absolute ΔΔG value, i.e., |ΔΔG|) has a significant, but not predictive, correlation with the pathogenicity of that variant. However, here we show that this correlation becomes significantly amplified in haploinsufficient genes. Moreover, the enrichment of pathogenic variants increases at the increasing protein stability perturbation value. These findings suggest that protein stability perturbation might be considered as a potential cofactor in diseases associated with haploinsufficient genes reporting missense variants.
错义变体是作为疾病生物标志物研究最多的基因组修饰之一。研究表明,错义变体导致的蛋白质稳定性“扰动”(以绝对ΔΔG值衡量,即|ΔΔG|)与该变体的致病性具有显著但非预测性的相关性。然而,我们在此表明,这种相关性在单倍剂量不足基因中会显著放大。此外,随着蛋白质稳定性扰动值的增加,致病变体的富集也会增加。这些发现表明,蛋白质稳定性扰动可能被视为与报告错义变体的单倍剂量不足基因相关疾病中的一种潜在辅助因素。