Program in Molecular Medicine, The Hospital for Sick Children, Toronto, ON M5G 0A4, Canada; Department of Biochemistry, University of Toronto, Toronto, ON M5S 1A8, Canada.
Program in Molecular Medicine, The Hospital for Sick Children, Toronto, ON M5G 0A4, Canada; Department of Cell & Systems Biology, University of Toronto, Toronto, ON M5S 3B2, Canada.
Cell. 2020 Dec 23;183(7):1742-1756. doi: 10.1016/j.cell.2020.11.050.
It is unclear how disease mutations impact intrinsically disordered protein regions (IDRs), which lack a stable folded structure. These mutations, while prevalent in disease, are frequently neglected or annotated as variants of unknown significance. Biomolecular phase separation, a physical process often mediated by IDRs, has increasingly appreciated roles in cellular organization and regulation. We find that autism spectrum disorder (ASD)- and cancer-associated proteins are enriched for predicted phase separation propensities, suggesting that IDR mutations disrupt phase separation in key cellular processes. More generally, we hypothesize that combinations of small-effect IDR mutations perturb phase separation, potentially contributing to "missing heritability" in complex disease susceptibility.
目前尚不清楚疾病突变如何影响缺乏稳定折叠结构的无规则蛋白区域(IDR)。这些突变虽然在疾病中很常见,但经常被忽视或注释为意义不明的变体。生物分子相分离是一种经常由 IDR 介导的物理过程,它在细胞组织和调控中扮演着越来越重要的角色。我们发现,自闭症谱系障碍(ASD)和癌症相关蛋白富含预测的相分离倾向,这表明 IDR 突变会破坏关键细胞过程中的相分离。更普遍地说,我们假设 IDR 突变的小效应组合会扰乱相分离,这可能是复杂疾病易感性中“遗传缺失”的原因之一。