NeuronMolecular BiologyPeer-reviewed journal article
Tau aggregates are RNA-protein assemblies that mis-localize multiple nuclear speckle components
Evan LesteriD, Felicia K. OoiiD, Nadine BakkariD, Jacob I. AyersiD, Amanda L. WoermaniD, Joshua WheeleriD, Robert P. BowseriD, George A. CarlsoniD, Stanley B. PrusineriD, Roy ParkeriD
Abstract
Tau aggregates contribute to neurodegenerative diseases including frontotemporal dementia and Alzheimers disease (AD). Although RNA promotes tau aggregation in vitro, whether tau aggregates in cells contain RNA is unknown. We demonstrate in cell culture and mouse brains that both cytosolic and nuclear tau aggregates contain RNA, with enrichment for snRNAs and snoRNAs. Nuclear tau aggregates colocalize with and alter the composition, dynamics, and organization of nuclear speckles, which are membraneless organelles involved in pre-mRNA splicing. Moreover, several nuclear speckle components, including SRRM2, mislocalize to cytosolic tau aggregates in cells, mouse brains, and patient brains with AD, frontotemporal dementia (FTD), and corticobasal degeneration (CBD). Consistent with these alterations we observe the presence of tau aggregates is sufficient to alter pre-mRNA splicing. This work identifies tau alteration of nuclear speckles as a feature of tau aggregation that may contribute to the pathology of tau aggregates.
- organism: mouse
- organism: human
- assay: proteomics
- assay: spatial transcriptomics
- research focus: cell type annotation
- research focus: differential expression
- research focus: gene regulatory network inference
- research focus: cell-cell communication
- approach: experimental assay
- Citations
- 218
- FWCI
- 21.97
- Field percentile
- top 1%
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