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BLOC1S1 variants cause lysosomal and autophagic defects resulting in a hypomyelinating leukodystrophy with epileptic encephalopathy

De Pace, R.; Dominguez Gonzalez, C. A.; Williamson, C.; Helman, G.; Sanderson, L. E.; Disanza, B.; Hsiao-Sanchez, N.; Pizzino, A.; Muirhead, K.; Bonkowsky, J. L.; Taft, R. J.; Sannaa, N. A.; Dias, P.; Quintas, A. S.; Burak Multu, M.; Bas, H.; Ozturk, H.; Mojarrad, M.; Alerasool, M.; Sheikhani, S.; Jabbar, H. K.; Issa, A. H.; Houlden, H.; Zonic, E.; Barakat, T. S.; Tripolski, K.; Romito, A.; Teferedegn, E.; Vossough, A.; Whitehead, M. T.; Bhoj, E.; Ahrens-Nicklas, R. C.; Simons, C.; Wolvetang, E.; van Ham, T. J.; Bertoli-Avella, A. M.; Maroofian, R.; Bonifacino, J. S.; Vanderver, A.

2025-07-17 genetic and genomic medicine
10.1101/2025.07.17.25331211 medRxiv
Show abstract

BLOC1S1 encodes a subunit shared by the BLOC-1 and BORC hetero-octameric complexes that regulate various endolysosomal processes. Here, we report the identification of seven distinct variants in BLOC1S1 in eleven individuals from seven independent families presenting with early psychomotor delay, hypotonia, spasticity, epileptic encephalopathy, optic atrophy, and leuko-axonopathy with hypomyelination. A subset of the affected individuals also have features of hypopigmentation and ocular albinism that are similar, although milder, than those of individuals with BLOC-1-related Hermansky-Pudlak syndrome. Functional analyses show that BLOC1S1 knockout (KO) impairs the anterograde transport of lysosomes and autophagy in both non-neuronal cells and iPSC-derived neurons. Rescue experiments reveal that most BLOC1S1 variants exhibit reduced expression, decreased assembly with other BORC/BLOC-1 subunits, and/or impaired restoration of lysosome transport and autophagy in BLOC1S1-KO cells. Additionally, we show that KO of BLOC1S1 reduces pigmentation in a melanocytic cell line, and that five of the BLOC1S1 variants partially or fully restore pigmentation. These findings provide genetic, clinical, and functional evidence that loss-of-function (LoF) of BLOC1S1 leads to more pronounced deficits in BORC than BLOC-1 function. We conclude that the biallelic BLOC1S1 variants characterized here primarily result in a neurological disorder with prominent leukodystrophy, similar to the recently reported condition caused by variants in the BORCS8 subunit of BORC. Together, these findings establish BORCopathies as a distinct disease entity.

Published in The American Journal of Human Genetics (predicted rank #1) · training set

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