engLoureiro, Joana RCastro, Ana FSousa, MafaldaDória, SofiaRizzu, PatriziaHeutink, PeterBessa, JoséSilveira, IsabelFigueiredo, Ana SEufrásio, AnaDhingra, AshutoshGalhardo, MafaldaMarcelino, HugoRodrigues, Catarina CSampaio, PaulaAzevedo, MariaThe insertion of an ATTTC repeat in an Alu element hyperactivates a neurodevelopmental enhancer in spinocerebellar ataxia type 37.info:eu-repo/classification/ddc/6104C-seqCAGECP: genomicsCP: neuroscienceDAB1 primate-specific Alu elementSCA37STRaxonal pathfindingcap analysis of gene expressioncerebellar transcriptional enhancercircularized chromosome conformation capture sequencingiPSNneurodegenerative diseasepentanucleotide repeat expansionshort tandem repeatspinocerebellar ataxia type 37Alu elements are evolutionarily very old primate-specific interspersed repeat elements that constitute ∼11% of the human genome. They are a source of short tandem repeats (STRs), which often expand in size and cause inherited neuromuscular and neurodegenerative disorders. How expanded STR insertion mutations within Alu STRs culminate in disease remains unknown. Here, we report an Alu STR located in an intron of DAB1 that functions as a neurodevelopmental enhancer. We demonstrate that an ATTTC repeat insertion in this DAB1 Alu STR, known to cause spinocerebellar ataxia type 37 (SCA37), hyperactivates a neurodevelopmental DAB1 enhancer. Importantly, we show that neurons derived from SCA37 subjects have higher levels of DAB1 expression and that DAB1 overexpression causes abnormal axonal pathfinding in vivo. Overall, these results establish that neuronal dysregulation of a developmental DAB1 Alu STR enhancer contributes to SCA37 pathogenesis, an unexplored mechanism likely acting in many Alu STR diseases, potentially reshaping the therapeutic landscape.Cell reports 45(4), 117146 (2026). doi:10.1016/j.celrep.2026.117146info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionCell Press2026info:eu-repo/semantics/closedAccessDEhttps://pub.dzne.de/record/286090https://pub.dzne.de/search?p=id:%22DZNE-2026-00386%22Researchersinfo:eu-repo/semantics/altIdentifier/issn/2211-1247info:eu-repo/semantics/altIdentifier/pmid/pmid:41871099info:eu-repo/semantics/altIdentifier/issn/2639-1856info:eu-repo/semantics/altIdentifier/doi/10.1016/j.celrep.2026.117146