Sublethal RNA Oxidation as a Mechanism for Neurodegenerative Disease

Although cellular RNA is subjected to the same oxidative insults as DNA and other cellular macromolecules, oxidative damage to RNA has not been a major focus in investigations of the biological consequences of free radical damage. In fact, because it is largely single-stranded and its bases lack the...

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Main Authors: Mark A. Smith, George Perry, Atsushi Takeda, Paula I. Moreira, Raj K. Rolston, Akihiko Nunomura, Rudy J. Castellani
Format: Article
Language:English
Published: MDPI AG 2008-05-01
Series:International Journal of Molecular Sciences
Subjects:
RNA
Online Access:http://www.mdpi.com/1422-0067/9/5/789/
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spelling doaj-f976bbf6b9d44e79840f0e73cf0e1baf2020-11-25T02:43:10ZengMDPI AGInternational Journal of Molecular Sciences1422-00672008-05-0195789806Sublethal RNA Oxidation as a Mechanism for Neurodegenerative DiseaseMark A. SmithGeorge PerryAtsushi TakedaPaula I. MoreiraRaj K. RolstonAkihiko NunomuraRudy J. CastellaniAlthough cellular RNA is subjected to the same oxidative insults as DNA and other cellular macromolecules, oxidative damage to RNA has not been a major focus in investigations of the biological consequences of free radical damage. In fact, because it is largely single-stranded and its bases lack the protection of hydrogen bonding and binding by specific proteins, RNA may be more susceptible to oxidative insults than is DNA. Oxidative damage to protein-coding RNA or non-coding RNA will, in turn, potentially cause errors in proteins and/or dysregulation of gene expression. While less lethal than mutations in the genome, such sublethal insults to cells might be associated with underlying mechanisms of several chronic diseases, including neurodegenerative disease. Recently, oxidative RNA damage has been described in several neurodegenerative diseases including Alzheimer disease, Parkinson disease, dementia with Lewy bodies, and prion diseases. Of particular interest, oxidative RNA damage can be demonstrated in vulnerable neurons early in disease, suggesting that RNA oxidation may actively contribute to the onset of the disease. An increasing body of evidence suggests that, mechanistically speaking, the detrimental effects of oxidative RNA damage to protein synthesis are attenuated, at least in part, by the existence of protective mechanisms that prevent the incorporation of the damaged ribonucleotides into the translational machinery. Further investigations aimed at understanding the processing mechanisms related to oxidative RNA damage and its consequences may provide significant insights into the pathogenesis of neurodegenerative and other degenerative diseases and lead to better therapeutic strategies.http://www.mdpi.com/1422-0067/9/5/789/Alzheimer disease8-oxoguanosineneurodegenerationoxidative damageParkinson diseaseRNA
collection DOAJ
language English
format Article
sources DOAJ
author Mark A. Smith
George Perry
Atsushi Takeda
Paula I. Moreira
Raj K. Rolston
Akihiko Nunomura
Rudy J. Castellani
spellingShingle Mark A. Smith
George Perry
Atsushi Takeda
Paula I. Moreira
Raj K. Rolston
Akihiko Nunomura
Rudy J. Castellani
Sublethal RNA Oxidation as a Mechanism for Neurodegenerative Disease
International Journal of Molecular Sciences
Alzheimer disease
8-oxoguanosine
neurodegeneration
oxidative damage
Parkinson disease
RNA
author_facet Mark A. Smith
George Perry
Atsushi Takeda
Paula I. Moreira
Raj K. Rolston
Akihiko Nunomura
Rudy J. Castellani
author_sort Mark A. Smith
title Sublethal RNA Oxidation as a Mechanism for Neurodegenerative Disease
title_short Sublethal RNA Oxidation as a Mechanism for Neurodegenerative Disease
title_full Sublethal RNA Oxidation as a Mechanism for Neurodegenerative Disease
title_fullStr Sublethal RNA Oxidation as a Mechanism for Neurodegenerative Disease
title_full_unstemmed Sublethal RNA Oxidation as a Mechanism for Neurodegenerative Disease
title_sort sublethal rna oxidation as a mechanism for neurodegenerative disease
publisher MDPI AG
series International Journal of Molecular Sciences
issn 1422-0067
publishDate 2008-05-01
description Although cellular RNA is subjected to the same oxidative insults as DNA and other cellular macromolecules, oxidative damage to RNA has not been a major focus in investigations of the biological consequences of free radical damage. In fact, because it is largely single-stranded and its bases lack the protection of hydrogen bonding and binding by specific proteins, RNA may be more susceptible to oxidative insults than is DNA. Oxidative damage to protein-coding RNA or non-coding RNA will, in turn, potentially cause errors in proteins and/or dysregulation of gene expression. While less lethal than mutations in the genome, such sublethal insults to cells might be associated with underlying mechanisms of several chronic diseases, including neurodegenerative disease. Recently, oxidative RNA damage has been described in several neurodegenerative diseases including Alzheimer disease, Parkinson disease, dementia with Lewy bodies, and prion diseases. Of particular interest, oxidative RNA damage can be demonstrated in vulnerable neurons early in disease, suggesting that RNA oxidation may actively contribute to the onset of the disease. An increasing body of evidence suggests that, mechanistically speaking, the detrimental effects of oxidative RNA damage to protein synthesis are attenuated, at least in part, by the existence of protective mechanisms that prevent the incorporation of the damaged ribonucleotides into the translational machinery. Further investigations aimed at understanding the processing mechanisms related to oxidative RNA damage and its consequences may provide significant insights into the pathogenesis of neurodegenerative and other degenerative diseases and lead to better therapeutic strategies.
topic Alzheimer disease
8-oxoguanosine
neurodegeneration
oxidative damage
Parkinson disease
RNA
url http://www.mdpi.com/1422-0067/9/5/789/
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