Intracellular translation of circular RNA

Abstract

A circular mRNA molecule possessing features resembling native mammalian mRNA demonstrates improved translation, while retaining the properties of an extremely long half-life inside cells. This circular mRNA is functional inside mammalian cells, being able to compete against native cellular mRNAs for the eukaryotic translation initiation machinery. The invention possesses additional RNA elements compared to a previous invention containing only an IRES element for successful in vitro or in vivo translation.

Description

PRIOR RELATED APPLICATIONS[0001]This application is a continuation of U.S. Ser. No. 14 / 890,799, now U.S. Pat. No. 9,822,378, filed on Nov. 12, 2015, which is a National Phase under 35 U.S.C. § 371 of International Application PCT / US2014 / 37795, filed May 13, 2014, which claims priority to U.S. Provisional Application 61 / 823,709, filed May 15, 2013. Each application is expressly incorporated in its entirety by reference herein for all purposes.FEDERALLY SPONSORED RESEARCH STATEMENT[0002]Not applicable.FIELD OF THE DISCLOSURE[0003]The disclosure generally relates to a biologic product comprising a circular RNA that is capable of translation inside a eukaryotic cell. The invention describes novel combinations of RNA elements that facilitate the enhanced translation and expression of encoded polypeptides, and provides vectors for making circular mRNA, as well as various applications using the circular mRNA and / or vector.BACKGROUND OF THE DISCLOSURE[0004]“Gene therapy” is the use of DNA a...

AI Technical Summary

Benefits of technology

[0025]One embodiment of the invention consists of a circular RNA molecule with modified RNA nucleotides. The possible modified ribonucleotide bases include 5-methylcytidine and pseudouridine. These nucleotides provide additional stability and resistance to immune activation.

[0057]In some embodiments the vector may also contain integration sequences, allowing for integration into a host genome, and such may be particularly preferred for cell based bioreactors because of increased stability.

Problems solved by technology

However, there are considerable technical difficulties to overcome before mRNA can be successfully used in various therapeutic methods.

This recognition leads to interferons being secreted, and if mRNA is attempted for repeated transfection, then ultimately cell death occurs via apoptosis.

Another difficulty has been the production of a complete and active mRNA via in vitro transcription.

In some cases, a 5′ cap is omitted and an IRES sequence utilized, but this is much more inefficient and reduces the half-life of the linear RNA molecule with no protection of the 5′ terminus of RNA.

Perhaps the biggest impediment, however, is the difficulty in handling mRNA.

RNA has two adjacent pendant hydroxyls on the pentose ring of the terminal nucleotide, making it very susceptible to nucleophilic attack by bases or by ever-present RNAses in water and on most surfaces.

RNAse-free reagents are used for the production of mRNA and its resultant storage, but even with such techniques, the extreme sensitivity to degradation presents considerably difficulty in implementing any RNA based technique.

Yet another impediment is the short half-life of mRNA once inside the cell.

However, circular RNA was originally thought to be unable to bind to eukaryotic ribosomes.

There was no data presented for the ability of a circular mRNA to translate in vivo inside a eukaryotic cell, and results in prokaryotes were disappointing.

However, this patent fails to describe the necessity of other regulatory elements in the circular RNA molecule for in vivo translation.

Indeed, there is no data demonstrating successful intracellular translation of circular mRNA in the patent or publication literature.

Furthermore, there were almost no follow-up reports in the literature demonstrating the utility of circular mRNA, in vitro or in vivo.

However, these patents fail to provide evidence of actual in vivo translation of the circular mRNA molecule.

Therefore, although possibly recognizing the potential of using circular mRNA for in vivo expression in eukaryotes, such applications were not in fact enabled.

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