DM1 repeat-expanded RNAs confer RNA toxicity as individual nuclear-retained RNAs

Repeat expansions of short nucleotide sequences underlie over 40 neuromuscular diseases, including myotonic dystrophy type 1 (DM1). The DM1 CUG repeat RNA is thought to accumulate in RNA nuclear foci that sequester RNA-binding proteins, including muscleblind-like splicing regulator 1 (MBNL1). To understand the composition and formation of such nuclear foci, we employed quantitative imaging in a patient-derived myotube model. We find that most "foci" are comprised of single RNAs and that these single RNA species contribute to the sequestration of MBNL1 protein. Rare foci can contain upwards of 25 distinct RNA species, but these foci form from transcriptional bursting and dissociate with time. Last, we find that multimeric CUG repeat RNA foci are dependent upon MBNL proteins. Altogether, these observations argue that the persistence of nuclear-retained CUG RNAs, independent of higher-order RNA assemblies, titrates MBNL1 and contributes to disease progression.

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Publication Details

Journal
Cell Reports
Published
2025-04-14
DOI
https://doi.org/10.1016/j.celrep.2025.115582
Citations
3
Primary Topic
RNA Research and Splicing
Type
article
Field-Weighted Citation Impact
2.42

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article

DM1 repeat-expanded RNAs confer RNA toxicity as individual nuclear-retained RNAs

John Paul T. Ouyang, Siddharth Shukla, Mona Bensalah
3 citations
Cell Reports
RNA Research and Splicing
2.42
article

DM1 repeat-expanded RNAs confer RNA toxicity as individual nuclear-retained RNAs

John Paul T. Ouyang, Siddharth Shukla, Mona Bensalah
article en
3 citations

Abstract

Repeat expansions of short nucleotide sequences underlie over 40 neuromuscular diseases, including myotonic dystrophy type 1 (DM1). The DM1 CUG repeat RNA is thought to accumulate in RNA nuclear foci that sequester RNA-binding proteins, including muscleblind-like splicing regulator 1 (MBNL1). To understand the composition and formation of such nuclear foci, we employed quantitative imaging in a patient-derived myotube model. We find that most "foci" are comprised of single RNAs and that these single RNA species contribute to the sequestration of MBNL1 protein. Rare foci can contain upwards of 25 distinct RNA species, but these foci form from transcriptional bursting and dissociate with time. Last, we find that multimeric CUG repeat RNA foci are dependent upon MBNL proteins. Altogether, these observations argue that the persistence of nuclear-retained CUG RNAs, independent of higher-order RNA assemblies, titrates MBNL1 and contributes to disease progression.

Cell ReportsVol. 44(5)
Howard Hughes Medical Institute (US), Inserm (FR), University of Colorado Boulder (US), Sorbonne Université (FR), Institut de Myologie (FR), Centre de Recherche en Myologie
Howard Hughes Medical Institute
Zero hunger
Openalex Percentile: Top 12%
RNA Research and Splicing
2.42
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