Emma L. Bunting,Jasmine Donaldson,Sarah A. Cumming,Jessica Olive,Elizabeth Broom,Mihai Miclăuș,Joseph Hamilton,Matthew Tegtmeyer,Hien Zhao,Jonathan Brenton,Won‐Seok Lee,Robert E. Handsaker,Susan Li,Brendon Ford,Mina Ryten,Steven A. McCarroll,Holly Kordasiewicz,Darren G. Monckton,Gabriel Balmus,Michael Flower,Sarah J. Tabrizi
出处
期刊:Science Translational Medicine [American Association for the Advancement of Science (AAAS)] 日期:2025-02-12卷期号:17 (785)
Expanded CAG alleles in the huntingtin ( HTT ) gene that cause the neurodegenerative disorder Huntington’s disease (HD) are genetically unstable and continue to expand somatically throughout life, driving HD onset and progression. MSH3, a DNA mismatch repair protein, modifies HD onset and progression by driving this somatic CAG repeat expansion process. MSH3 is relatively tolerant of loss-of-function variation in humans, making it a potential therapeutic target. Here, we show that an MSH3 -targeting antisense oligonucleotide (ASO) effectively engaged with its RNA target in induced pluripotent stem cell (iPSC)–derived striatal neurons obtained from a patient with HD carrying 125 HTT CAG repeats (the 125 CAG iPSC line). ASO treatment led to a dose-dependent reduction of MSH3 and subsequent stalling of CAG repeat expansion in these striatal neurons. Bulk RNA sequencing revealed a safe profile for MSH3 reduction, even when reduced by >95%. Maximal knockdown of MSH3 also effectively slowed CAG repeat expansion in striatal neurons with an otherwise accelerated expansion rate, derived from the 125 CAG iPSC line where FAN1 was knocked out by CRISPR-Cas9 editing. Last, we created a knock-in mouse model expressing the human MSH3 gene and demonstrated effective in vivo reduction in human MSH3 after ASO treatment. Our study shows that ASO-mediated MSH3 reduction can prevent HTT CAG repeat expansion in HD 125 CAG iPSC–derived striatal neurons, highlighting the therapeutic potential of this approach.