Cited by 766RNA and protein synthesis mechanismsCircular RNAs in diseasesRNA Research and Splicing

Initiation of Protein Synthesis by the Eukaryotic Translational Apparatus on Circular RNAs

Chen, Chang-you, Sarnow, Peter·1995·Science

Abstract

The ribosome scanning model predicts that eukaryotic ribosomal 40 S subunits enter all messenger RNAs at their 5′ ends. Here, it is reported that eukaryotic ribosomes can initiate translation on circular RNAs, but only if the RNAs contain internal ribosome entry site elements. Long-repeating polypeptide chains were synthesized from RNA circles with continuous open reading frames. These results indicate that ribosomes can translate such RNA circles for multiple consecutive rounds and that the free 5′ end of a messenger RNA is not necessarily the entry point for 40 S subunits.

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Crossref · 10.1126/science.7536344

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  • Although circRNA was initially thought not to serve as a translational template, later reports contradicted this hypothesis.

    “Although it was initially thought not to serve as a translational template, later reports contradicted this hypothesis, triggering further research.48”

    From COVID-19 mRNA vaccines: Platforms and current developments (2022) · cites this paper as [48]

  • circRNA can be translated in eukaryotic cells and, due to its closed-ring structure, is significantly more resistant to exonuclease-mediated degradation compared with linear mRNA.

    “circRNA (also called endless RNA) can be translated in eukaryotic cells48 and, due to its closed-ring structure, is significantly more resistant to exonuclease-mediated degradation compared with linear mRNA.151”

    From COVID-19 mRNA vaccines: Platforms and current developments (2022) · cites this paper as [48]

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Authors
Chen, C.-Y., & Sarnow, P.
Affiliations
  • Molecular Biology Program, Department of Biochemistry, Biophysics and Genetics, Dyde Laboratory, University of Colorado Health Sciences Center, Denver, CO 80262, USA.
  • University of Colorado Health (US)
Venue
Science
Published
1995-04-21
Volume
268
Issue
5209
Pages
415-417
ISSN
  • 0036-8075 (ISSN-L)
  • 1095-9203
OpenAlex
W2094813328
Cited by
766
References
1
Citations by year
2026: 21 · 2025: 59 · 2024: 54 · 2023: 46 · 2022: 68 · 2021: 85 · 2020: 83 · 2019: 47 · 2018: 51 · 2017: 36 · 2016: 28 · 2015: 22 · 2014: 12 · 2013: 12 · 2012: 9
FWCI
5.09
Type
journal article
Language
en
Open access
closed
Locations
  • Science (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA and protein synthesis mechanisms
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Circular RNAs in diseases
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA Research and Splicing
Keywords
circular RNA, internal ribosome entry site, translation initiation, 80S ribosome, 40S ribosomal subunit, open reading frames, polypeptide synthesis
MeSH terms
RNA, Circular, Codon, Encephalomyocarditis virus, Peptide Chain Initiation, Translational, Ribosomes, RNA, RNA, Messenger, Templates, Genetic, Protein Biosynthesis, Open Reading Frames

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