Splice modulators target PMS1 to reduce somatic expansion of the Huntington's disease-associated CAG repeat.
Zachariah L McLeanDadi GaoKevin CorreiaJennie C L RoyShota ShibataIris N FarnumZoe Valdepenas-MellorMarina KovalenkoManasa RapuruElisabetta MoriniJayla RulieraTammy GillisDiane LucenteBenjamin P KleinstiverJong-Min LeeMarcy E MacDonaldVanessa C WheelerRicardo Mouro PintoJames F GusellaPublished in: Nature communications (2024)
Huntington's disease (HD) is a dominant neurological disorder caused by an expanded HTT exon 1 CAG repeat that lengthens huntingtin's polyglutamine tract. Lowering mutant huntingtin has been proposed for treating HD, but genetic modifiers implicate somatic CAG repeat expansion as the driver of onset. We find that branaplam and risdiplam, small molecule splice modulators that lower huntingtin by promoting HTT pseudoexon inclusion, also decrease expansion of an unstable HTT exon 1 CAG repeat in an engineered cell model. Targeted CRISPR-Cas9 editing shows this effect is not due to huntingtin lowering, pointing instead to pseudoexon inclusion in PMS1. Homozygous but not heterozygous inactivation of PMS1 also reduces CAG repeat expansion, supporting PMS1 as a genetic modifier of HD and a potential target for therapeutic intervention. Although splice modulation provides one strategy, genome-wide transcriptomics also emphasize consideration of cell-type specific effects and polymorphic variation at both target and off-target sites.