Loss of TDP-43 function drives cryptic circular RNAs in neurodegenerative diseases

Authors

Zhu, C., Zhao, Z., Song, B., Chen, Y.-M., Xiao, Y., Zhang, Z., Ye, Y., Xu, N., Zhang, R., Huang, Y., Troncoso, J. C., He, C., Sun, S.

Abstract

TAR DNA-binding protein 43 (TDP-43) is a key pathological hallmark of amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) and a critical regulator of RNA splicing. While loss of TDP-43 induces aberrant splicing in linear transcripts, its impact on circular RNA (circRNA) biogenesis remains unexplored. Here, we show that TDP-43 depletion in human neurons induces widespread circRNA changes, especially upregulation of a distinct class of cryptic circRNAs that arise specifically upon loss of TDP-43. Some of these cryptic circRNAs incorporate cryptic exons derived from intronic sequences. Notably, these cryptic circRNAs exhibit greater stability than their corresponding linear RNA isoforms and accumulate progressively in neurons. Moreover, cryptic circRNAs are elevated in postmortem brain tissues from ALS, FTD and Alzheimer's disease (AD) patients. These findings reveal a previously unrecognized role for TDP-43 in repressing cryptic circRNA formation and establish these circRNAs as stable molecular signatures of TDP-43 dysfunction.

Preprint server: bioRxiv
The authors list and abstract were imported from bioRxiv on 21 Sep 2026.

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