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Synthesis and biological activity of artificial mRNA prepared with novel phosphorylating reagents.


ABSTRACT: Though medicines that target mRNA are under active investigation, there has been little or no effort to develop mRNA itself as a medicine. Here, we report the synthesis of a 130-nt mRNA sequence encoding a 33-amino-acid peptide that includes the sequence of glucagon-like peptide-1, a peptide that stimulates glucose-dependent insulin secretion from the pancreas. The synthesis method used, which had previously been developed in our laboratory, was based on the use of 2-cyanoethoxymethyl as the 2'-hydroxy protecting group. We also developed novel, highly reactive phosphotriester pyrophosphorylating reagents to pyrophosphorylate the 5'-end of the 130-mer RNA in preparation for capping. We completed the synthesis of the artificial mRNA by the enzymatic addition of a 5'-cap and a 3'-poly(A) tail to the pyrophosphorylated 130-mer and showed that the resulting mRNA supported protein synthesis in a cell-free system and in whole cells. As far as we know, this is the first time that mRNA has been prepared from a chemically synthesized RNA sequence. As well as providing a research tool for the intracellular expression of peptides, the technology described here may be used for the production of mRNA for medical applications.

SUBMITTER: Nagata S 

PROVIDER: S-EPMC2995060 | biostudies-literature | 2010 Nov

REPOSITORIES: biostudies-literature

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Synthesis and biological activity of artificial mRNA prepared with novel phosphorylating reagents.

Nagata Seigo S   Hamasaki Tomohiro T   Uetake Koichi K   Masuda Hirofumi H   Takagaki Kazuchika K   Oka Natsuhisa N   Wada Takeshi T   Ohgi Tadaaki T   Yano Junichi J  

Nucleic acids research 20100726 21


Though medicines that target mRNA are under active investigation, there has been little or no effort to develop mRNA itself as a medicine. Here, we report the synthesis of a 130-nt mRNA sequence encoding a 33-amino-acid peptide that includes the sequence of glucagon-like peptide-1, a peptide that stimulates glucose-dependent insulin secretion from the pancreas. The synthesis method used, which had previously been developed in our laboratory, was based on the use of 2-cyanoethoxymethyl as the 2'-  ...[more]

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