Discovery of a mutation-containing circRNA in polyglutamine disease through systematic analysis of RNAs with CAG repeats

CAG repeat tracts occur in both non-coding and translated RNAs, have tended to lengthen throughout evolution, and are thought to enhance neuronal function. We identified over 600 human RNAs (including mRNAs, lncRNAs, and circRNAs) with at least 10 CAG repeats, originating from 58 genomic loci, which vary, e.g. in the rate of CAG length polymorphism. Several circRNAs originate from the ATXN7 locus, where CAG expansion causes spinocerebellar ataxia type 7 (SCA7). For selected circATXN7(3,4).1 (circ1), we demonstrated its cytoplasmic localization, as well as its presence in 40S, monosome and polysome fractions. We showed that circ1 is expressed in human fibroblasts, blood and cerebellum, and, importantly, we identified a mutation-containing circRNA with potential implications in SCA7.

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Journal
RNA Biology
Published
2026-06-24
DOI
https://doi.org/10.1080/15476286.2026.2684791
Primary Topic
Genetic Neurodegenerative Diseases
Type
article
Field-Weighted Citation Impact
0.00

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Discovery of a mutation-containing circRNA in polyglutamine disease through systematic analysis of RNAs with CAG repeats

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Discovery of a mutation-containing circRNA in polyglutamine disease through systematic analysis of RNAs with CAG repeats

Tomasz M. Witkos, Jarosław Sławek, Agata Ciołak, Julien Philippe, Luke C. Bartelt, Jarosław Dulski, Magdalena Jazurek, Paweł M. Świtoński, Emilia Kozłowska, Albert R. La Spada, Edyta Kościańska, M. Woźna, Agnieszka Fiszer, Weronika Pawlik
article en

Abstract

CAG repeat tracts occur in both non-coding and translated RNAs, have tended to lengthen throughout evolution, and are thought to enhance neuronal function. We identified over 600 human RNAs (including mRNAs, lncRNAs, and circRNAs) with at least 10 CAG repeats, originating from 58 genomic loci, which vary, e.g. in the rate of CAG length polymorphism. Several circRNAs originate from the ATXN7 locus, where CAG expansion causes spinocerebellar ataxia type 7 (SCA7). For selected circATXN7(3,4).1 (circ1), we demonstrated its cytoplasmic localization, as well as its presence in 40S, monosome and polysome fractions. We showed that circ1 is expressed in human fibroblasts, blood and cerebellum, and, importantly, we identified a mutation-containing circRNA with potential implications in SCA7.

RNA BiologyVol. 23(1)
University of California System (US), Duke Medical Center (US), Institute of Bioorganic Chemistry, Polish Academy of Sciences (PL), Gdańsk Medical University (PL)
National Ataxia Foundation, Narodowym Centrum Nauki, National Institutes of Health, European Regional Development Fund, National Institute on Aging
Openalex Percentile: Top 10%
Genetic Neurodegenerative Diseases
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