Skip to Main content Skip to Navigation
Journal articles

RNA editing alterations define manifestation of prion diseases

Abstract : Prion diseases are fatal neurodegenerative disorders caused by misfolding of the normal prion protein into an infectious cellular pathogen. Clinically characterized by rapidly progressive dementia and accounting for 85% of human prion disease cases, sporadic Creutzfeldt-Jakob disease (sCJD) is the prevalent human prion disease. Although sCJD neuropathological hallmarks are well-known, associated molecular alterations are elusive due to rapid progression and absence of preclinical stages. To investigate transcriptome alterations during disease progression, we utilized tg340-PRNP129MM mice infected with postmortem material from sCJD patients of the most susceptible genotype (MM1 subtype), a sCJD model that faithfully recapitulates the molecular and pathological alterations of the human disease. Here we report that transcriptomic analyses from brain cortex in the context of disease progression, reveal epitranscriptomic alterations (specifically altered RNA edited pathway profiles, eg., ER stress, lysosome) that are characteristic and possibly protective mainly for preclinical and clinical disease stages. Our results implicate regulatory epitranscriptomic mechanisms in prion disease neuropathogenesis, whereby RNA-editing targets in a humanized sCJD mouse model were confirmed in pathological human autopsy material.
Document type :
Journal articles
Complete list of metadata

https://hal.inrae.fr/hal-03199348
Contributor : Christopher Lallemant <>
Submitted on : Saturday, April 24, 2021 - 5:44:00 PM
Last modification on : Friday, July 9, 2021 - 10:08:02 AM

File

pnas-09-2019.pdf
Files produced by the author(s)

Licence


Distributed under a Creative Commons Attribution - NonCommercial - NoDerivatives 4.0 International License

Identifiers

Collections

Citation

Eirini Kanata, Franc Llorens, Dimitra Dafou, Athanasios Dimitriadis, Katrin Thüne, et al.. RNA editing alterations define manifestation of prion diseases. Proceedings of the National Academy of Sciences of the United States of America , National Academy of Sciences, 2019, 116 (39), pp.19727-19735. ⟨10.1073/pnas.1803521116⟩. ⟨hal-03199348⟩

Share

Metrics

Record views

65

Files downloads

92