Autism-related traits in myotonic dystrophy type 1 model mice are due to MBNL sequestration and RNA mis-splicing of autism-risk genes

Genome-wide enrichment of gene-specific tandem repeat expansions has been linked to autism spectrum disorder. One such mutation is the CTG tandem repeat expansion in the 3' untranslated region of the DMPK gene, which is known to cause myotonic muscular dystrophy type 1. Although there is a clear clinical association between autism and myotonic dystrophy, the molecular basis for this connection remains unknown. Here, we report that sequestration of MBNL splicing factors by mutant DMPK RNAs with expanded CUG repeats alters the RNA splicing patterns of autism-risk genes during brain development, particularly a class of autism-relevant microexons. We demonstrate that both DMPK-CTG expansion and Mbnl null mouse models recapitulate autism-relevant mis-splicing profiles, along with social behavioral deficits and altered responses to novelty. These findings support our model that myotonic dystrophy-associated autism arises from developmental mis-splicing of autism-risk genes.

Authors

Institutions

Publication Details

Journal
Nature Neuroscience
Published
2025-04-21
DOI
https://doi.org/10.1038/s41593-025-01943-0
Citations
7
Primary Topic
Genetic Neurodegenerative Diseases
Type
article
Field-Weighted Citation Impact
6.36

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Autism-related traits in myotonic dystrophy type 1 model mice are due to MBNL sequestration and RNA mis-splicing of autism-risk genes

Curtis A. Nutter, Katarzyna Taylor, Mahreen Khan, Ryan K. C. Yuen et al.
7 citations
Nature Neuroscience
Genetic Neurodegenerative Diseases
6.36
article

Autism-related traits in myotonic dystrophy type 1 model mice are due to MBNL sequestration and RNA mis-splicing of autism-risk genes

Curtis A. Nutter, Katarzyna Taylor, Mahreen Khan, Ryan K. C. Yuen, Maurice S. Swanson, Christopher E. Pearson, Adam Ciesiołka, Krzysztof Sobczak, Mark H. Lewis, Łukasz J. Sznajder, Mariam Tadross, Rochelle M. Hines
article en
7 citations

Abstract

Genome-wide enrichment of gene-specific tandem repeat expansions has been linked to autism spectrum disorder. One such mutation is the CTG tandem repeat expansion in the 3' untranslated region of the DMPK gene, which is known to cause myotonic muscular dystrophy type 1. Although there is a clear clinical association between autism and myotonic dystrophy, the molecular basis for this connection remains unknown. Here, we report that sequestration of MBNL splicing factors by mutant DMPK RNAs with expanded CUG repeats alters the RNA splicing patterns of autism-risk genes during brain development, particularly a class of autism-relevant microexons. We demonstrate that both DMPK-CTG expansion and Mbnl null mouse models recapitulate autism-relevant mis-splicing profiles, along with social behavioral deficits and altered responses to novelty. These findings support our model that myotonic dystrophy-associated autism arises from developmental mis-splicing of autism-risk genes.

Nature NeuroscienceVol. 28(6)
University of Nevada, Las Vegas (US), University of Toronto (CA), Hospital for Sick Children (CA), University of Florida (US), SickKids Foundation (CA), Adam Mickiewicz University in Poznań (PL), Florida College (US)
Myotonic Dystrophy Foundation, Muscular Dystrophy Association, University of Nevada, Las Vegas, Narodowe Centrum Nauki, Azrieli Foundation, Canadian Institutes of Health Research, National Institute of General Medical Sciences, National Institute of Neurological Disorders and Stroke
Reduced inequalities
Openalex Percentile: Top 3%
Genetic Neurodegenerative Diseases
6.36
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.