| Literature DB >> 33357399 |
Brian Tsang1, Iva Pritišanac2, Stephen W Scherer3, Alan M Moses4, Julie D Forman-Kay5.
Abstract
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.Entities:
Keywords: Phase separation; autism spectrum disorder; biomolecular condensates; cancer; intrinsic disorder; intrinsically disordered protein regions; neurodevelopment
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Year: 2020 PMID: 33357399 DOI: 10.1016/j.cell.2020.11.050
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582