In Vivo Formation of Vacuolated Multi-phase Compartments Lacking Membranes

Eukaryotic cells contain membrane-less organelles, including nucleoli and stress granules, that behave like liquid droplets. Such endogenous condensates often have internal substructure, but how this is established in the absence of membrane encapsulation remains unclear. We find that the N- and C-t...

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Main Authors: Hermann Broder Schmidt, Rajat Rohatgi
Format: Article
Language:English
Published: Elsevier 2016-08-01
Series:Cell Reports
Online Access:http://www.sciencedirect.com/science/article/pii/S2211124716308579
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spelling doaj-67a88d68ecc247acb2e2b5f39a74bb6e2020-11-24T22:09:20ZengElsevierCell Reports2211-12472016-08-011651228123610.1016/j.celrep.2016.06.088In Vivo Formation of Vacuolated Multi-phase Compartments Lacking MembranesHermann Broder Schmidt0Rajat Rohatgi1Department of Biochemistry, Stanford University School of Medicine, Stanford, CA 94305, USADepartment of Biochemistry, Stanford University School of Medicine, Stanford, CA 94305, USAEukaryotic cells contain membrane-less organelles, including nucleoli and stress granules, that behave like liquid droplets. Such endogenous condensates often have internal substructure, but how this is established in the absence of membrane encapsulation remains unclear. We find that the N- and C-terminal domains of TDP43, a heterogeneous nuclear ribonucleoprotein implicated in neurodegenerative diseases, are capable of driving the formation of sub-structured liquid droplets in vivo. These droplets contain dynamic internal “bubbles” of nucleoplasm, reminiscent of membrane-based multi-vesicular endosomes. A conserved sequence embedded within the intrinsically disordered region (IDR) of TDP43 promotes the formation of these multi-phase assemblies. Disease-causing point mutations in the IDR can change the propensity to form bubbles, protein dynamics within the phase, or phase-environment exchange rates. Our results show that a single IDR-containing protein can nucleate the assembly of compartmentalized liquid droplets approximating the morphological complexity of membrane-bound organelles.http://www.sciencedirect.com/science/article/pii/S2211124716308579
collection DOAJ
language English
format Article
sources DOAJ
author Hermann Broder Schmidt
Rajat Rohatgi
spellingShingle Hermann Broder Schmidt
Rajat Rohatgi
In Vivo Formation of Vacuolated Multi-phase Compartments Lacking Membranes
Cell Reports
author_facet Hermann Broder Schmidt
Rajat Rohatgi
author_sort Hermann Broder Schmidt
title In Vivo Formation of Vacuolated Multi-phase Compartments Lacking Membranes
title_short In Vivo Formation of Vacuolated Multi-phase Compartments Lacking Membranes
title_full In Vivo Formation of Vacuolated Multi-phase Compartments Lacking Membranes
title_fullStr In Vivo Formation of Vacuolated Multi-phase Compartments Lacking Membranes
title_full_unstemmed In Vivo Formation of Vacuolated Multi-phase Compartments Lacking Membranes
title_sort in vivo formation of vacuolated multi-phase compartments lacking membranes
publisher Elsevier
series Cell Reports
issn 2211-1247
publishDate 2016-08-01
description Eukaryotic cells contain membrane-less organelles, including nucleoli and stress granules, that behave like liquid droplets. Such endogenous condensates often have internal substructure, but how this is established in the absence of membrane encapsulation remains unclear. We find that the N- and C-terminal domains of TDP43, a heterogeneous nuclear ribonucleoprotein implicated in neurodegenerative diseases, are capable of driving the formation of sub-structured liquid droplets in vivo. These droplets contain dynamic internal “bubbles” of nucleoplasm, reminiscent of membrane-based multi-vesicular endosomes. A conserved sequence embedded within the intrinsically disordered region (IDR) of TDP43 promotes the formation of these multi-phase assemblies. Disease-causing point mutations in the IDR can change the propensity to form bubbles, protein dynamics within the phase, or phase-environment exchange rates. Our results show that a single IDR-containing protein can nucleate the assembly of compartmentalized liquid droplets approximating the morphological complexity of membrane-bound organelles.
url http://www.sciencedirect.com/science/article/pii/S2211124716308579
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