Literature DB >> 30531905

Acetylation of intrinsically disordered regions regulates phase separation.

Makoto Saito1,2, Daniel Hess1, Jan Eglinger1, Anatol W Fritsch3,4, Moritz Kreysing3,4, Brian T Weinert5, Chunaram Choudhary5, Patrick Matthias6,7.   

Abstract

Liquid-liquid phase separation (LLPS) of proteins containing intrinsically disordered regions (IDRs) has been proposed as a mechanism underlying the formation of membrane-less organelles. Tight regulation of IDR behavior is essential to ensure that LLPS only takes place when necessary. Here, we report that IDR acetylation/deacetylation regulates LLPS and assembly of stress granules (SGs), membrane-less organelles forming in response to stress. Acetylome analysis revealed that the RNA helicase DDX3X, an important component of SGs, is a novel substrate of the deacetylase HDAC6. The N-terminal IDR of DDX3X (IDR1) can undergo LLPS in vitro, and its acetylation at multiple lysine residues impairs the formation of liquid droplets. We also demonstrated that enhanced LLPS propensity through deacetylation of DDX3X-IDR1 by HDAC6 is necessary for SG maturation, but not initiation. Our analysis provides a mechanistic framework to understand how acetylation and deacetylation of IDRs regulate LLPS spatiotemporally, and impact membrane-less organelle formation in vivo.

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Year:  2018        PMID: 30531905     DOI: 10.1038/s41589-018-0180-7

Source DB:  PubMed          Journal:  Nat Chem Biol        ISSN: 1552-4450            Impact factor:   15.040


  65 in total

1.  Stress granule formation, disassembly, and composition are regulated by alphavirus ADP-ribosylhydrolase activity.

Authors:  Aravinth Kumar Jayabalan; Srivathsan Adivarahan; Aakash Koppula; Rachy Abraham; Mona Batish; Daniel Zenklusen; Diane E Griffin; Anthony K L Leung
Journal:  Proc Natl Acad Sci U S A       Date:  2021-02-09       Impact factor: 11.205

Review 2.  Friend or foe-Post-translational modifications as regulators of phase separation and RNP granule dynamics.

Authors:  Mario Hofweber; Dorothee Dormann
Journal:  J Biol Chem       Date:  2018-12-26       Impact factor: 5.157

Review 3.  Protein phase separation: A novel therapy for cancer?

Authors:  Wei Wang; Yingqian Chen; Aixiao Xu; Minyi Cai; Ji Cao; Hong Zhu; Bo Yang; Xuejing Shao; Meidan Ying; Qiaojun He
Journal:  Br J Pharmacol       Date:  2020-09-28       Impact factor: 8.739

4.  Binding of inhibitors to active-site mutants of CD1, the enigmatic catalytic domain of histone deacetylase 6.

Authors:  Jeremy D Osko; David W Christianson
Journal:  Acta Crystallogr F Struct Biol Commun       Date:  2020-08-19       Impact factor: 1.056

5.  Liquid-Liquid Phase Separation of Histone Proteins in Cells: Role in Chromatin Organization.

Authors:  Anisha Shakya; Seonyoung Park; Neha Rana; John T King
Journal:  Biophys J       Date:  2019-12-31       Impact factor: 4.033

Review 6.  Acetate Metabolism in Physiology, Cancer, and Beyond.

Authors:  Shree Bose; Vijyendra Ramesh; Jason W Locasale
Journal:  Trends Cell Biol       Date:  2019-05-31       Impact factor: 20.808

Review 7.  Biomolecular Phase Separation: From Molecular Driving Forces to Macroscopic Properties.

Authors:  Gregory L Dignon; Robert B Best; Jeetain Mittal
Journal:  Annu Rev Phys Chem       Date:  2020-04-20       Impact factor: 12.703

Review 8.  Considerations and Challenges in Studying Liquid-Liquid Phase Separation and Biomolecular Condensates.

Authors:  Simon Alberti; Amy Gladfelter; Tanja Mittag
Journal:  Cell       Date:  2019-01-24       Impact factor: 41.582

Review 9.  Physiological, Pathological, and Targetable Membraneless Organelles in Neurons.

Authors:  Veronica H Ryan; Nicolas L Fawzi
Journal:  Trends Neurosci       Date:  2019-09-05       Impact factor: 13.837

10.  Structural Basis of Catalysis and Inhibition of HDAC6 CD1, the Enigmatic Catalytic Domain of Histone Deacetylase 6.

Authors:  Jeremy D Osko; David W Christianson
Journal:  Biochemistry       Date:  2019-12-02       Impact factor: 3.162

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