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Phase Transition of a Disordered Nuage Protein Generates Environmentally Responsive Membraneless Organelles
Cells chemically isolate molecules in compartments to both facilitate and regulate their interactions. In addition to membrane-encapsulated compartments, cells can form proteinaceous and membraneless organelles, including nucleoli, Cajal and PML bodies, and stress granules. The principles that deter...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4352761/ https://www.ncbi.nlm.nih.gov/pubmed/25747659 http://dx.doi.org/10.1016/j.molcel.2015.01.013 |
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author | Nott, Timothy J. Petsalaki, Evangelia Farber, Patrick Jervis, Dylan Fussner, Eden Plochowietz, Anne Craggs, Timothy D. Bazett-Jones, David P. Pawson, Tony Forman-Kay, Julie D. Baldwin, Andrew J. |
author_facet | Nott, Timothy J. Petsalaki, Evangelia Farber, Patrick Jervis, Dylan Fussner, Eden Plochowietz, Anne Craggs, Timothy D. Bazett-Jones, David P. Pawson, Tony Forman-Kay, Julie D. Baldwin, Andrew J. |
author_sort | Nott, Timothy J. |
collection | PubMed |
description | Cells chemically isolate molecules in compartments to both facilitate and regulate their interactions. In addition to membrane-encapsulated compartments, cells can form proteinaceous and membraneless organelles, including nucleoli, Cajal and PML bodies, and stress granules. The principles that determine when and why these structures form have remained elusive. Here, we demonstrate that the disordered tails of Ddx4, a primary constituent of nuage or germ granules, form phase-separated organelles both in live cells and in vitro. These bodies are stabilized by patterned electrostatic interactions that are highly sensitive to temperature, ionic strength, arginine methylation, and splicing. Sequence determinants are used to identify proteins found in both membraneless organelles and cell adhesion. Moreover, the bodies provide an alternative solvent environment that can concentrate single-stranded DNA but largely exclude double-stranded DNA. We propose that phase separation of disordered proteins containing weakly interacting blocks is a general mechanism for forming regulated, membraneless organelles. |
format | Online Article Text |
id | pubmed-4352761 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-43527612015-03-31 Phase Transition of a Disordered Nuage Protein Generates Environmentally Responsive Membraneless Organelles Nott, Timothy J. Petsalaki, Evangelia Farber, Patrick Jervis, Dylan Fussner, Eden Plochowietz, Anne Craggs, Timothy D. Bazett-Jones, David P. Pawson, Tony Forman-Kay, Julie D. Baldwin, Andrew J. Mol Cell Article Cells chemically isolate molecules in compartments to both facilitate and regulate their interactions. In addition to membrane-encapsulated compartments, cells can form proteinaceous and membraneless organelles, including nucleoli, Cajal and PML bodies, and stress granules. The principles that determine when and why these structures form have remained elusive. Here, we demonstrate that the disordered tails of Ddx4, a primary constituent of nuage or germ granules, form phase-separated organelles both in live cells and in vitro. These bodies are stabilized by patterned electrostatic interactions that are highly sensitive to temperature, ionic strength, arginine methylation, and splicing. Sequence determinants are used to identify proteins found in both membraneless organelles and cell adhesion. Moreover, the bodies provide an alternative solvent environment that can concentrate single-stranded DNA but largely exclude double-stranded DNA. We propose that phase separation of disordered proteins containing weakly interacting blocks is a general mechanism for forming regulated, membraneless organelles. Cell Press 2015-03-05 /pmc/articles/PMC4352761/ /pubmed/25747659 http://dx.doi.org/10.1016/j.molcel.2015.01.013 Text en © 2015 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Nott, Timothy J. Petsalaki, Evangelia Farber, Patrick Jervis, Dylan Fussner, Eden Plochowietz, Anne Craggs, Timothy D. Bazett-Jones, David P. Pawson, Tony Forman-Kay, Julie D. Baldwin, Andrew J. Phase Transition of a Disordered Nuage Protein Generates Environmentally Responsive Membraneless Organelles |
title | Phase Transition of a Disordered Nuage Protein Generates Environmentally Responsive Membraneless Organelles |
title_full | Phase Transition of a Disordered Nuage Protein Generates Environmentally Responsive Membraneless Organelles |
title_fullStr | Phase Transition of a Disordered Nuage Protein Generates Environmentally Responsive Membraneless Organelles |
title_full_unstemmed | Phase Transition of a Disordered Nuage Protein Generates Environmentally Responsive Membraneless Organelles |
title_short | Phase Transition of a Disordered Nuage Protein Generates Environmentally Responsive Membraneless Organelles |
title_sort | phase transition of a disordered nuage protein generates environmentally responsive membraneless organelles |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4352761/ https://www.ncbi.nlm.nih.gov/pubmed/25747659 http://dx.doi.org/10.1016/j.molcel.2015.01.013 |
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