The nucleolus functions as a phase-separated protein quality control compartment

Author:

Frottin F.1ORCID,Schueder F.23ORCID,Tiwary S.4ORCID,Gupta R.1ORCID,Körner R.1,Schlichthaerle T.23,Cox J.4ORCID,Jungmann R.23ORCID,Hartl F. U.15ORCID,Hipp M. S.15ORCID

Affiliation:

1. Department of Cellular Biochemistry, Max Planck Institute of Biochemistry, D-82152 Martinsried, Germany.

2. Research Group “Molecular Imaging and Bionanotechnology,” Max Planck Institute of Biochemistry, D-82152 Martinsried, Germany.

3. Faculty of Physics and Center for Nanoscience, Ludwig Maximilian University, D-80539 Munich, Germany.

4. Research Group “Computational Systems Biochemistry,” Max Planck Institute of Biochemistry, D-82152 Martinsried, Germany.

5. Munich Cluster for Systems Neurology (SyNergy), D-80336 Munich, Germany.

Abstract

Phasing-in quality control in the nucleus The fundamental process of protein quality control in the nucleus is not well understood. The nucleus contains several non–membrane-bound subcompartments forming liquid-like condensates. The largest of these is the nucleolus, the site of ribosome biogenesis. Frottin et al. found that metastable nuclear proteins that misfold upon heat stress enter the nucleolus. In the nucleolus, they avoid irreversible aggregation and remain competent for heat shock protein 70–dependent refolding upon recovery from stress. Prolonged stress or the uptake of proteins associated with neurodegenerative diseases prevented this reversibility. Thus, the properties of a phase-separated compartment can assist in protein quality control. Science , this issue p. 342

Funder

European Molecular Biology Organization

European Research Council

Deutsche Forschungsgemeinschaft

Max Planck Foundation

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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