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- W2805750982 abstract "Intrinsically disordered regions occur frequently in proteins and are characterized by a lack of a well-defined three-dimensional structure. Although these regions do not show a higher order of structural organization, they are known to be functionally important. Disordered regions are rapidly evolving, largely attributed to relaxed purifying selection and an increased role of genetic drift. It has also been suggested that positive selection might contribute to their rapid diversification. However, for our own species, it is currently unknown whether positive selection has played a role during the evolution of these protein regions. Here, we address this question by investigating the evolutionary pattern of more than 6600 human proteins with intrinsically disordered regions and their ordered counterparts. Our comparative approach with data from more than 90 mammalian genomes uses a priori knowledge of disordered protein regions, and we show that this increases the power to detect positive selection by an order of magnitude. We can confirm that human intrinsically disordered regions evolve more rapidly, not only within humans but also across the entire mammalian phylogeny. They have, however, experienced substantial evolutionary constraint, hinting at their fundamental functional importance. We find compelling evidence that disordered protein regions are frequent targets of positive selection and estimate that the relative rate of adaptive substitutions differs fourfold between disordered and ordered protein regions in humans. Our results suggest that disordered protein regions are important targets of genetic innovation and that the contribution of positive selection in these regions is more pronounced than in other protein parts." @default.
- W2805750982 created "2018-06-13" @default.
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- W2805750982 date "2018-06-01" @default.
- W2805750982 modified "2023-10-12" @default.
- W2805750982 title "Human long intrinsically disordered protein regions are frequent targets of positive selection" @default.
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- W2805750982 doi "https://doi.org/10.1101/gr.232645.117" @default.
- W2805750982 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/6028134" @default.
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- W2805750982 hasPublicationYear "2018" @default.
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