Abstract
Biomolecular condensation arising through phase transitions has emerged as an essential organizational strategy that governs many aspects of cell biology. In particular, the role of phase transitions in the assembly of large, complex ribonucleoprotein (RNP) granules has become appreciated as an important regulator of RNA metabolism. In parallel, genetic, histopathological and cell and molecular studies have provided evidence that disturbance of phase transitions is an important driver of neurological diseases, notably amyotrophic lateral sclerosis (ALS), but most likely also other diseases. Indeed, our growing knowledge of the biophysics underlying biological phase transitions suggests that this process offers a unifying mechanism to explain the numerous and diverse disturbances in RNA metabolism that have been observed in ALS and some related diseases — specifically, that these diseases are driven by disturbances in the material properties of RNP granules. Here, we review the evidence for this hypothesis, emphasizing the reciprocal roles in which disease-related protein and disease-related RNA can lead to disturbances in the material properties of RNP granules and consequent pathogenesis. Additionally, we review evidence that implicates aberrant phase transitions as a contributing factor to a larger set of neurodegenerative diseases, including frontotemporal dementia, certain repeat expansion diseases and Alzheimer disease.
Key points
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Intracellular phase transition describes a biophysical phenomenon in which macromolecules separate from their aqueous surroundings to form a functional compartment.
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Biomolecular condensation arising through phase transitions is a cellular organizational strategy that governs many aspects of cell biology.
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Among the largest biomolecular condensates are ribonucleoprotein (RNP) granules — membraneless organelles composed of RNA and protein — which regulate nearly all aspects of RNA metabolism.
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Genetic, histopathological, cellular and molecular studies of amyotrophic lateral sclerosis (ALS) and related diseases have identified dysfunction in diverse aspects of RNA metabolism as a common theme.
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Aberrant phase transitions and disturbances of the material properties of RNP granules offer a unifying mechanism for the numerous disturbances in RNA metabolism observed in ALS and related diseases.
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Acknowledgements
J.P.T.’s research work is funded by the Howard Hughes Medical Institute and the St Jude Research Collaborative on the Biology of Membraneless Organelles.
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Nedelsky, N.B., Taylor, J.P. Bridging biophysics and neurology: aberrant phase transitions in neurodegenerative disease. Nat Rev Neurol 15, 272–286 (2019). https://doi.org/10.1038/s41582-019-0157-5
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DOI: https://doi.org/10.1038/s41582-019-0157-5
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