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mRNA and circRNA mislocalization to synapses are key features of Alzheimer's disease.
Smukowski, Samuel N; Danyko, Cassidy; Somberg, Jenna; Kaufman, Eli J; Course, Meredith M; Postupna, Nadia; Barker-Haliski, Melissa; Keene, C Dirk; Valdmanis, Paul N.
Afiliación
  • Smukowski SN; Division of Medical Genetics, Department of Medicine, University of Washington, Seattle, WA, United States of America.
  • Danyko C; Department of Genome Sciences, University of Washington, Seattle, Washington, United States of America.
  • Somberg J; Division of Medical Genetics, Department of Medicine, University of Washington, Seattle, WA, United States of America.
  • Kaufman EJ; Fred Hutch Cancer Center, Basic Sciences Division, University of Washington, Seattle, Washington, United States of America.
  • Course MM; Division of Medical Genetics, Department of Medicine, University of Washington, Seattle, WA, United States of America.
  • Postupna N; Department of Laboratory Medicine and Pathology, University of Washington School of Medicine, Seattle, Washington, United States of America.
  • Barker-Haliski M; Division of Medical Genetics, Department of Medicine, University of Washington, Seattle, WA, United States of America.
  • Keene CD; Division of Medical Genetics, Department of Medicine, University of Washington, Seattle, WA, United States of America.
  • Valdmanis PN; Department of Molecular Biology, Colorado College, Colorado Springs, Colorado, United States of America.
PLoS Genet ; 20(7): e1011359, 2024 Jul.
Article en En | MEDLINE | ID: mdl-39074152
ABSTRACT
Proper transport of RNAs to synapses is essential for localized translation of proteins in response to synaptic signals and synaptic plasticity. Alzheimer's disease (AD) is a neurodegenerative disease characterized by accumulation of amyloid aggregates and hyperphosphorylated tau neurofibrillary tangles followed by widespread synapse loss. To understand whether RNA synaptic localization is impacted in AD, we performed RNA sequencing on synaptosomes and brain homogenates from AD patients and cognitively healthy controls. This resulted in the discovery of hundreds of mislocalized mRNAs in AD among frontal and temporal brain regions. Similar observations were found in an APPswe/PSEN1dE9 mouse model. Furthermore, major differences were observed among circular RNAs (circRNAs) localized to synapses in AD including two overlapping isoforms of circGSK3ß, one upregulated, and one downregulated. Expression of these distinct isoforms affected tau phosphorylation in neuronal cells substantiating the importance of circRNAs in the brain and pointing to a new class of therapeutic targets.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Sinapsis / ARN Mensajero / Proteínas tau / Enfermedad de Alzheimer / ARN Circular Límite: Aged / Animals / Female / Humans / Male Idioma: En Revista: PLoS Genet Asunto de la revista: GENETICA Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Sinapsis / ARN Mensajero / Proteínas tau / Enfermedad de Alzheimer / ARN Circular Límite: Aged / Animals / Female / Humans / Male Idioma: En Revista: PLoS Genet Asunto de la revista: GENETICA Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos