Establishment of a second-generation transgenic marmoset model of polyglutamine disease recapitulating neurological symptoms and pathology

Minakawa, E. N.; Owari, K.; Nogami, N.; Nakatani, T.; Koizumi, M.; Kawanobe, A.; Saga, Y.; Kudo, M.; Noguchi, S.; Hanakawa, T.; Hori, Y.; Numazawa, H.; Takeuchi, T.; Katakai, Y.; Saito, R.; Nagai, Y.; Saito, Y.; Tomioka, I.; Seki, K.

doi:10.1101/2025.03.12.642922

bioRxiv · 10.1101/2025.03.12.642922

Establishment of a second-generation transgenic marmoset model of polyglutamine disease recapitulating neurological symptoms and pathology

Minakawa, E. N.·Owari, K.·Nogami, N.·Nakatani, T.·Koizumi, M.·Kawanobe, A.·Saga, Y.·Kudo, M.·Noguchi, S.·Hanakawa, T.·Hori, Y.·Numazawa, H.·Takeuchi, T.·Katakai, Y.·Saito, R.·Nagai, Y.·Saito, Y.·Tomioka, I.·Seki, K.

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Abstract

Neurodegenerative diseases, including polyglutamine diseases, remain a major clinical challenge, partly because of limited animal models that recapitulate human disease. Here, we describe a second-generation transgenic marmoset model of spinocerebellar ataxia 3 (SCA3), a polyglutamine disease, which stably expresses expanded CAG repeats in ATXN3. All five offspring of the founder marmoset harbored the transgene with reduced transgene integration sites and without repeat instability or genetic mosaicism, offering improved construct validity. Three of the five marmosets developed progressive motor impairments that segregated into two distinct phenotypes: early onset with rapid progression and late onset with mild progression, accompanied by corresponding patterns in body weight gain and grip strength. Pathological analysis revealed cerebellar Purkinje cell loss, spinal cord neurodegeneration, and widespread intranuclear inclusions. The severity of motor phenotypes correlated with transgene expression levels in disease-relevant brain regions, including the cerebellum, spinal cord, and striatum. By overcoming the common translational limitations of rodent systems, our second-generation model offers a powerful platform for investigating disease mechanisms and testing potential therapeutic interventions. Our results advance the utility of transgenic marmosets as clinically relevant models of neurodegenerative diseases. Summary StatementSecond-generation transgenic marmoset models of spinocerebellar ataxia 3 replicated the progressive motor deficits and neuropathology of the founder marmoset, providing a powerful platform for studying disease mechanisms and developing therapies.

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Minakawa, E. N., Owari, K., Nogami, N., Nakatani, T., Koizumi, M., Kawanobe, A., Saga, Y., Kudo, M., Noguchi, S., Hanakawa, T., Hori, Y., Numazawa, H., Takeuchi, T., Katakai, Y., Saito, R., Nagai, Y., Saito, Y., Tomioka, I., Seki, K.. 2025-03-13. Establishment of a second-generation transgenic marmoset model of polyglutamine disease recapitulating neurological symptoms and pathology. https://doi.org/10.1101/2025.03.12.642922

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