PreprintCited by 16RNA regulation and diseaseRNA Research and SplicingRNA and protein synthesis mechanisms

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The Role of C-to-U RNA Editing in Human Biodiversity

Open access
Van Norden, Melissa, Falls, Zackary, Mandloi, Sapan, Segal, Brahm, Baysal, Bora, Samudrala, Ram, Elkin, Peter L.·2023·Communications Biology

Preprint — published as 10.1038/s42003-024-06239-w

Abstract

Intra-organism biodiversity is thought to arise from epigenetic modification of our constituent genes and post-translational modifications after mRNA is translated into proteins. We have found that post-transcriptional modification, also known as RNA editing, is also responsible for a significant amount of our biodiversity, substantively expanding this story. The APOBEC (apolipoprotein B mRNA editing catalytic polypeptide-like) family RNA editing enzymes APOBEC3A and APOBEC3G catalyze the deamination of cytosines to uracils (C>U) in specific stem-loop structures. 1,2 We used RNAsee (RNA site editing evaluation), a tool developed to predict the locations of APOBEC3A/G RNA editing sites, to determine whether known single nucleotide polymorphisms (SNPs) in DNA could be replicated in RNA via RNA editing. About 4.5% of non-synonymous SNPs which result in C>U changes in RNA, and about 5.4% of such SNPs labelled as pathogenic, were identified as probable sites for APOBEC3A/G editing. This suggests that the variant proteins created by these DNA mutations may also be created by transient RNA editing, with the potential to affect human health. Those SNPs identified as potential APOBEC3A/G-mediated RNA editing sites were disproportionately associated with cardiovascular diseases, digestive system diseases, and musculoskeletal diseases. Future work should focus on common sites of RNA editing, any variant proteins created by these RNA editing sites, and the effects of these variants on protein diversity and human health. Classically, our biodiversity is thought to come from our constitutive genetics, epigenetic phenomenon, transcriptional differences, and post-translational modification of proteins. Here, we have shown evidence that RNA editing, often stimulated by environmental factors, could account for a significant degree of the protein biodiversity leading to human disease. In an era where worries about our changing environment are ever increasing, from the warming of our climate to the emergence of new diseases to the infiltration of microplastics and pollutants into our bodies, understanding how environmentally sensitive mechanisms like RNA editing affect our own cells is essential.

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Metadata

Authors
Van Norden, M., Falls, Z., Mandloi, S., Segal, B., Baysal, B., Samudrala, R., & Elkin, P. L.
Affiliations
  • University at Buffalo, State University of New York (US)
  • Roswell Park Comprehensive Cancer Center (US)
  • University of Southern Denmark (DK)
Corresponding author
Elkin, Peter L.
Venue
Communications Biology
Publisher
openRxiv
Published
2023-07-31
Volume
7
Issue
1
Pages
529-529
ISSN
2399-3642 (ISSN-L)
OpenAlex
W4396637483
Cited by
16
References
1
Citations by year
2026: 7 · 2025: 8 · 2024: 1
FWCI
2.18
Type
journal article
Language
en
Open access
Licence
cc-by
Locations
  • Communications Biology (publishedVersion, cc-by)
  • bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion, cc-by)
  • Research Square (acceptedVersion, cc-by)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • University of Southern Denmark Research Portal (University of Southern Denmark) (publishedVersion, cc-by)
  • PubMed Central (submittedVersion, cc-by)
  • DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
Funders
  • U.S. Department of Health and Human Services (LMR1514213, LMT15012495, LMT1512495)
  • U.S. Department of Veterans Affairs (UL1TR001412)
  • National Institutes of Health (UL1TR001412)
  • National Institute of Standards and Technology (60NANB22D168)
  • University at Buffalo (UL1TR001412)
  • National Institute on Alcohol Abuse and Alcoholism (R21AA026954, R33AA0226954)
  • National Institute on Drug Abuse (K01DA056690)
  • U.S. National Library of Medicine (LMT15012495, LMR1514213, LMT1512495, T15LM012495, R25LM014213)
  • National Center for Advancing Translational Sciences
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA regulation and disease
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA Research and Splicing
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA and protein synthesis mechanisms
Keywords
APOBEC3A, APOBEC3G, C-to-U RNA editing, cytosine deamination, single nucleotide polymorphisms, post-transcriptional modification, disease association, human disease

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