Circular RNA, the Key for Translation.
Int J Mol Sci
; 21(22)2020 Nov 14.
Article
en En
| MEDLINE
| ID: mdl-33202605
ABSTRACT
It was thought until the 1990s that the eukaryotic translation machinery was unable to translate a circular RNA. However internal ribosome entry sites (IRESs) and m6A-induced ribosome engagement sites (MIRESs) were discovered, promoting 5' end-independent translation initiation. Today a new family of so-called "noncoding" circular RNAs (circRNAs) has emerged, revealing the pivotal role of 5' end-independent translation. CircRNAs have a strong impact on translational control via their sponge function, and form a new mRNA family as they are translated into proteins with pathophysiological roles. While there is no more doubt about translation of covalently closed circRNA, the linearity of canonical mRNA is only theoretical it has been shown for more than thirty years that polysomes exhibit a circular form and mRNA functional circularization has been demonstrated in the 1990s by the interaction of initiation factor eIF4G with poly(A) binding protein. More recently, additional mechanisms of 3'-5' interaction have been reported, including m6A modification. Functional circularization enhances translation via ribosome recycling and acceleration of the translation initiation rate. This update of covalently and noncovalently closed circular mRNA translation landscape shows that RNA with circular shape might be the rule for translation with an important impact on disease development and biotechnological applications.
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Texto completo:
1
Banco de datos:
MEDLINE
Asunto principal:
Ribosomas
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Biosíntesis de Proteínas
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ARN Mensajero
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Sitios Internos de Entrada al Ribosoma
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ARN Circular
Límite:
Humans
Idioma:
En
Año:
2020
Tipo del documento:
Article