Compact Calm1 promoter enables AAV mediated neuron-targeted expression in human iPSC-derived brain organoids

Compact neuron-specific promoters enable targeted gene expression in the brain, especially when using size-limited adeno-associated virus (AAV) vectors. The human synapsin 1 gene promoter (hSyn) promoter is widely used, but the recently described Calm1 promoter (120 bp long) offers a smaller alternative with demonstrated excitatory and inhibitory neuron-specificity in animal models. Here, we compared the commonly used hSyn promoter and the compact Calm1 promoter in human iPSC-derived brain organoids using AAV reporter constructs. Our study evaluating reporter gene expression and immunohistology showed comparable performance in human neurons. Our findings suggest that the compact Calm1 promoter could be used for future central nervous system-targeted human gene therapies.

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Publication Details

Journal
Scientific Reports
Published
2025-12-24
DOI
https://doi.org/10.1038/s41598-025-28162-8
Primary Topic
Virus-based gene therapy research
Type
article
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article

Compact Calm1 promoter enables AAV mediated neuron-targeted expression in human iPSC-derived brain organoids

Jason L. Stein, M. Zylka, Meghana Yeturi, Trinity E Rust et al.
Scientific Reports
Virus-based gene therapy research
article

Compact Calm1 promoter enables AAV mediated neuron-targeted expression in human iPSC-derived brain organoids

Jason L. Stein, M. Zylka, Meghana Yeturi, Trinity E Rust, Ina Klockner
article en

Abstract

Compact neuron-specific promoters enable targeted gene expression in the brain, especially when using size-limited adeno-associated virus (AAV) vectors. The human synapsin 1 gene promoter (hSyn) promoter is widely used, but the recently described Calm1 promoter (120 bp long) offers a smaller alternative with demonstrated excitatory and inhibitory neuron-specificity in animal models. Here, we compared the commonly used hSyn promoter and the compact Calm1 promoter in human iPSC-derived brain organoids using AAV reporter constructs. Our study evaluating reporter gene expression and immunohistology showed comparable performance in human neurons. Our findings suggest that the compact Calm1 promoter could be used for future central nervous system-targeted human gene therapies.

Scientific ReportsVol. 15(1)
University of North Carolina at Chapel Hill (US), University of North Carolina Health Care (US)
Good health and well-being
Openalex Percentile: Top 25%
Virus-based gene therapy research
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