Abstract

The bright fluorescent cytosine analogue tCO stands out among fluorescent bases due to its virtually unquenched fluorescence emission in duplex DNA. However, like most reported base analogues, it has not been thoroughly characterized in RNA. We here report on the first synthesis and RNA-incorporation of tCO, and characterize its base-mimicking and fluorescence properties in RNA. As in DNA, we find a high quantum yield inside RNA duplexes (<ΦF> = 0.22) that is virtually unaffected by the neighbouring bases (ΦF = 0.20–0.25), resulting in an average brightness of 1900 M−1 cm−1. The average fluorescence lifetime in RNA duplexes is 4.3 ns and generally two lifetimes are required to fit the exponential decays. Fluorescence properties in ssRNA are defined by a small increase in average quantum yield (<ΦF > = 0.24) compared to dsRNA, with a broader distribution (ΦF = 0.17–0.34) and slightly shorter average lifetimes. Using circular dichroism, we find that the tCO-modified RNA duplexes form regular A-form helices and in UV-melting experiments the stability of the duplexes is only slightly higher than that of the corresponding natural RNA (<ΔTm> = + 2.3 °C). These properties make tCO a highly interesting fluorescent RNA base analogue for detailed FRET-based structural measurements, as a bright internal label in microscopy, and for fluorescence anisotropy measurements of RNA dynamics.

Highlights

  • IntroductionNon-perturbing fluorescent probe is employed, real-time information on the structure and intrinsic dynamics of nucleic acids may be obtained[12, 18], which could pave the way towards a deeper understanding of important cellular processes such as the genome editing CRISPR systems[19,20,21,22,23]

  • A-form helices and in UV-melting experiments the stability of the duplexes is only slightly higher than that of the corresponding natural RNA ( = + 2.3 °C)

  • The discovery two decades ago that short RNA sequences can up- or downregulate gene expression through the RNA interference (RNAi)[1] pathway sparked high hopes for gene silencing with antisense oligonucleotides (ASOs)[2, 3], but while RNAi reagents such as siRNA have provided a wealth of information on gene function[4], their utility in antisense therapy have so far been limited by stability and delivery challenges[2,3,4]

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Summary

Introduction

Non-perturbing fluorescent probe is employed, real-time information on the structure and intrinsic dynamics of nucleic acids may be obtained[12, 18], which could pave the way towards a deeper understanding of important cellular processes such as the genome editing CRISPR systems[19,20,21,22,23]. It may support the Street, Dundee, DD1 5EH, UK. Development of novel oligonucleotide-based therapeutics, such as ASOs, through visualisation of their intercellular transport and subcellular localisation[2]

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