Abstract

RNA 5′-modifications are known to extend the functional spectrum of ribonucleotides. In recent years, numerous non-canonical 5′-modifications, including adenosine-containing cofactors from the group of B vitamins, have been confirmed in all kingdoms of life. The structural component of thiamine adenosine triphosphate (thiamine-ATP), a vitamin B1 derivative found to accumulate in Escherichia coli and other organisms in response to metabolic stress conditions, suggests an analogous function as a 5′-modification of RNA. Here, we report the synthesis of thiamine adenosine dinucleotides and the preparation of pure 5′-thiamine-capped RNAs based on phosphorimidazolide chemistry. Furthermore, we present the incorporation of thiamine-ATP and thiamine adenosine diphosphate (thiamine-ADP) as 5′-caps of RNA by T7 RNA polymerase. Transcripts containing the thiamine modification were modified specifically with biotin via a combination of thiazole ring opening, nucleophilic substitution and copper-catalyzed azide-alkyne cycloaddition. The highlighted methods provide easy access to 5′-thiamine RNA, which may be applied in the development of thiamine-specific RNA capture protocols as well as the discovery and confirmation of 5′-thiamine-capped RNAs in various organisms.

Highlights

  • Ribonucleic acid (RNA) obtains remarkable structural and functional versatility through the combination of the four canonical ribonucleosides adenosine (A), guanosine (G), cytidine (C) and uridine (U)

  • The approaches we have demonstrated allow for the in vitro preparation of 50 -thiamine RNA, approaches demonstrated allow for of thespecific in vitro preparation of 5′-thiamine

  • Adenosine-containing thiamine derivatives have been successfully synthesized by imidazolide-based activation of phosphate groups of the respective thiamine or adenosine species

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Summary

Introduction

Ribonucleic acid (RNA) obtains remarkable structural and functional versatility through the combination of the four canonical ribonucleosides adenosine (A), guanosine (G), cytidine (C) and uridine (U). Numerous additional modifications occur internally as well as terminally, at the 30 - and 50 -end, and fine-tune the functional spectrum of RNA. Such modifications can, e.g., increase the stability of RNA against degradation processes, extend the catalytic activity of ribozymes, promote RNA interactions with other molecules or assume various regulatory roles within the cellular environment [1,2,3,4,5,6]. A post-transcriptional modification of messenger RNA (mRNA) with a 7-methylguanosine (m7G) cap takes place [7,8]. The m7G cap and similar structures provide increased stability of mRNA against

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