Condensation properties of stress granules and processing bodies are compromised in myotonic dystrophy type 1

Author:

Gulyurtlu Selma1,Magon Monika S.1,Guest Patrick1,Papavasiliou Panagiotis P.1,Morrison Kim D.1,Prescott Alan R.2ORCID,Sleeman Judith E.1ORCID

Affiliation:

1. Biomolecular Sciences Research Complex, School of Biology, University of St Andrews 1 , North Haugh, St Andrews, Fife KY16 9ST , UK

2. Division of Cell Signalling and Immunology, School of Life Science, University of Dundee 2 , Dundee DD1 5EH , UK

Abstract

ABSTRACT RNA regulation in mammalian cells requires complex physical compartmentalisation, using structures thought to be formed by liquid-liquid phase separation. Disruption of these structures is implicated in numerous degenerative diseases. Myotonic dystrophy type 1 (DM1) is a multi-systemic trinucleotide repeat disorder resulting from an expansion of nucleotides CTG (CTGexp) in the DNA encoding DM1 protein kinase (DMPK). The cellular hallmark of DM1 is the formation of nuclear foci that contain expanded DMPK RNA (CUGexp) (with thymine instead of uracil). We report here the deregulation of stress granules (SGs) and processing bodies (P-bodies), two cytoplasmic structures key for mRNA regulation, in cell culture models of DM1. Alterations to the rates of formation and dispersal of SGs suggest an altered ability of cells to respond to stress associated with DM1, while changes to the structure and dynamics of SGs and P-bodies suggest that a widespread alteration to the biophysical properties of cellular structures is a consequence of the presence of CUGexp RNA.

Funder

Muscular Dystrophy UK

Biotechnology and Biological Sciences Research Council

Wellcome Trust

Publisher

The Company of Biologists

Subject

General Biochemistry, Genetics and Molecular Biology,Immunology and Microbiology (miscellaneous),Medicine (miscellaneous),Neuroscience (miscellaneous)

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