4.7 Article

Protein Aggregation and Disaggregation in Cells and Development

Journal

JOURNAL OF MOLECULAR BIOLOGY
Volume 433, Issue 21, Pages -

Publisher

ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
DOI: 10.1016/j.jmb.2021.167215

Keywords

biomolecular condensate; amyloid; chaperone; ABCF gene family; RuvBL gene family

Funding

  1. University of Iowa Office of the Vice President
  2. University of Iowa Center for Biocatalysis and Biotechnology grant
  3. NIH [GM114007, GM124063]
  4. NSF-IOS [1917169]
  5. Division Of Integrative Organismal Systems
  6. Direct For Biological Sciences [1917169] Funding Source: National Science Foundation

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Protein aggregation is a characteristic of many neurodegenerative diseases, but it can also regulate cellular activities such as stress response, gene expression, and cell development. This review explores examples of protein aggregates in biological systems and cellular strategies for controlling aggregation and disassembly.
Protein aggregation is a feature of numerous neurodegenerative diseases. However, regulated, often reversible, formation of protein aggregates, also known as condensates, helps control a wide range of cellular activities including stress response, gene expression, memory, cell development and differentiation. This review presents examples of aggregates found in biological systems, how they are used, and cellular strategies that control aggregation and disaggregation. We include features of the aggregating proteins themselves, environmental factors, co-aggregates, post-translational modifications and well-known aggregation-directed activities that influence their formation, material state, stability and dissolution. We highlight the emerging roles of biomolecular condensates in early animal development, and disaggregation processing proteins that have recently been shown to play key roles in gametogenesis and embryogenesis. (C) 2021 Elsevier Ltd. All rights reserved.

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