Key result
Interaction between poly-A binding protein and cap-binding complex promotes translation initiation via circular mRNA conformation.
This review highlights the paradigm shift in understanding mRNA translation initiation, emphasizing the role of PABP in forming circular mRNAs.
May inform circular mRNA therapeutic design; leaves open prospective validation before clinical use.
In recent years, our thinking of how the initiation of protein synthesis occurs has changed dramatically. Initiation was thought to involve only events occurring at or near the 5′-cap structure, which serves as the binding site for the cap-binding complex, a group of translation initiation factors (eIFs) that facilitate the binding of the 40 S ribosomal subunit to an mRNA. Because the poly(A)-binding protein (PABP) binds the poly(A) tail present at the 3′-terminus of an mRNA, it was long thought to play no role in translation initiation. In this review, I present evidence from my laboratory that has contributed to the paradigm shift in how we think of mRNAs during translation. The depiction of mRNAs as straight molecules in which the poly(A) tail is far from events occurring at the 5′-end has now been replaced by the concept of a circular mRNA where the interaction between PABP and the cap-binding complex bridges the termini of an mRNA and promotes translation initiation. The research from my laboratory supports the new paradigm that translation of most mRNAs requires a functional and physical interaction between the termini of an mRNA.
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Daniel Gallie (2014) conducted a review in mRNA translation. The interaction between the poly(A)-binding protein and the cap-binding complex bridges the termini of an mRNA, promoting translation initiation through a circular mRNA conformation.
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