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Protein-coding circular RNAs – mechanism, detection, and their role in cancer and neurodegenerative diseases.
- Source :
-
Biochemical & Biophysical Research Communications . Oct2023, Vol. 678, p68-77. 10p. - Publication Year :
- 2023
-
Abstract
- Circular RNAs (circRNAs) are a unique class of non-coding RNAs and were originally thought to have no protein-coding potential due to their lack of a 5′ cap and 3′ poly(A) tail. However, recent studies have challenged this notion and revealed that some circRNAs have protein-coding potential. They have emerged as a key area of interest in cancer and neurodegeneration research as recent studies have identified several circRNAs that can produce functional proteins with important roles in cancer progression. The protein-coding potential of circRNAs is determined by the presence of an open reading frame (ORF) within the circular structure that can encode a protein. In some cases, the ORF can be translated into a functional protein despite the lack of traditional mRNA features. While the protein-coding potential of most circRNAs remains unclear, several studies have identified specific circRNAs that can produce functional proteins. Understanding the protein-coding potential of circRNAs is important for unravelling their biological functions and potential roles in disease. Our review provides comprehensive coverage of recent advances in the field of circRNA protein-coding capacity and its impact on cancer and neurodegenerative diseases pathogenesis and progression. • Circular RNAs are functionally important component of the human transcriptome. • Protein-coding capacity of circular RNAs may impact regulation of gene expression. • Circular RNAs represent a potential target for molecular diagnosis of cancer and neurodegenerative diseases. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 0006291X
- Volume :
- 678
- Database :
- Academic Search Index
- Journal :
- Biochemical & Biophysical Research Communications
- Publication Type :
- Academic Journal
- Accession number :
- 171920199
- Full Text :
- https://doi.org/10.1016/j.bbrc.2023.08.037