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Circular RNA Encoded Amyloid Beta peptides—A Novel Putative Player in Alzheimer’s Disease

Alzheimer’s disease (AD) is an age-related detrimental dementia. Amyloid beta peptides (Aβ) play a crucial role in the pathology of AD. In familial AD, Aβ are generated from the full-length amyloid beta precursor protein (APP) via dysregulated proteolytic processing; however, in the case of sporadic...

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Autores principales: Mo, Dingding, Li, Xinping, Raabe, Carsten A., Rozhdestvensky, Timofey S., Skryabin, Boris V., Brosius, Juergen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7650678/
https://www.ncbi.nlm.nih.gov/pubmed/33003364
http://dx.doi.org/10.3390/cells9102196
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author Mo, Dingding
Li, Xinping
Raabe, Carsten A.
Rozhdestvensky, Timofey S.
Skryabin, Boris V.
Brosius, Juergen
author_facet Mo, Dingding
Li, Xinping
Raabe, Carsten A.
Rozhdestvensky, Timofey S.
Skryabin, Boris V.
Brosius, Juergen
author_sort Mo, Dingding
collection PubMed
description Alzheimer’s disease (AD) is an age-related detrimental dementia. Amyloid beta peptides (Aβ) play a crucial role in the pathology of AD. In familial AD, Aβ are generated from the full-length amyloid beta precursor protein (APP) via dysregulated proteolytic processing; however, in the case of sporadic AD, the mechanism of Aβ biogenesis remains elusive. circRNAs are a class of transcripts preferentially expressed in brain. We identified a circRNA harboring the Aβ-coding region of the APP gene termed circAβ-a. This circular RNA was detected in the brains of AD patients and non-dementia controls. With the aid of our recently established approach for analysis of circRNA functions, we demonstrated that circAβ-a is efficiently translated into a novel Aβ-containing Aβ175 polypeptide (19.2 KDa) in both cultured cells and human brain. Furthermore, Aβ175 was shown to be processed into Aβ peptides—a hallmark of AD. In summary, our analysis revealed an alternative pathway of Aβ biogenesis. Consequently, circAβ-a and its corresponding translation product could potentially represent novel therapeutic targets for AD treatment. Importantly, our data point to yet another evolutionary route for potentially increasing proteome complexity by generating additional polypeptide variants using back-splicing of primary transcripts that yield circular RNA templates.
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spelling pubmed-76506782020-11-10 Circular RNA Encoded Amyloid Beta peptides—A Novel Putative Player in Alzheimer’s Disease Mo, Dingding Li, Xinping Raabe, Carsten A. Rozhdestvensky, Timofey S. Skryabin, Boris V. Brosius, Juergen Cells Article Alzheimer’s disease (AD) is an age-related detrimental dementia. Amyloid beta peptides (Aβ) play a crucial role in the pathology of AD. In familial AD, Aβ are generated from the full-length amyloid beta precursor protein (APP) via dysregulated proteolytic processing; however, in the case of sporadic AD, the mechanism of Aβ biogenesis remains elusive. circRNAs are a class of transcripts preferentially expressed in brain. We identified a circRNA harboring the Aβ-coding region of the APP gene termed circAβ-a. This circular RNA was detected in the brains of AD patients and non-dementia controls. With the aid of our recently established approach for analysis of circRNA functions, we demonstrated that circAβ-a is efficiently translated into a novel Aβ-containing Aβ175 polypeptide (19.2 KDa) in both cultured cells and human brain. Furthermore, Aβ175 was shown to be processed into Aβ peptides—a hallmark of AD. In summary, our analysis revealed an alternative pathway of Aβ biogenesis. Consequently, circAβ-a and its corresponding translation product could potentially represent novel therapeutic targets for AD treatment. Importantly, our data point to yet another evolutionary route for potentially increasing proteome complexity by generating additional polypeptide variants using back-splicing of primary transcripts that yield circular RNA templates. MDPI 2020-09-29 /pmc/articles/PMC7650678/ /pubmed/33003364 http://dx.doi.org/10.3390/cells9102196 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Mo, Dingding
Li, Xinping
Raabe, Carsten A.
Rozhdestvensky, Timofey S.
Skryabin, Boris V.
Brosius, Juergen
Circular RNA Encoded Amyloid Beta peptides—A Novel Putative Player in Alzheimer’s Disease
title Circular RNA Encoded Amyloid Beta peptides—A Novel Putative Player in Alzheimer’s Disease
title_full Circular RNA Encoded Amyloid Beta peptides—A Novel Putative Player in Alzheimer’s Disease
title_fullStr Circular RNA Encoded Amyloid Beta peptides—A Novel Putative Player in Alzheimer’s Disease
title_full_unstemmed Circular RNA Encoded Amyloid Beta peptides—A Novel Putative Player in Alzheimer’s Disease
title_short Circular RNA Encoded Amyloid Beta peptides—A Novel Putative Player in Alzheimer’s Disease
title_sort circular rna encoded amyloid beta peptides—a novel putative player in alzheimer’s disease
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7650678/
https://www.ncbi.nlm.nih.gov/pubmed/33003364
http://dx.doi.org/10.3390/cells9102196
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