Abstract

DNA topology plays essential roles in several fundamental biological processes, such as DNA replication, recombination, and transcription. Typically agarose gel electrophoresis is employed to study DNA topology. Since gel electrophoresis is time-consuming and labor intensive, it is desirable to develop other methods, such as fluorescence-based methods, for such studies. In this paper we report the synthesis of a type of unique fluorescence-labeled DNA molecules that can be used to study DNA topology and topoisomerases by fluorescence resonance energy transfer (FRET). Specifically, we inserted an 82 nt. synthetic DNA oligomer FL905 carrying a 42 nt. AT sequence with fluorescein and dabcyl labels into a gapped DNA molecule to generate relaxed and supercoiled pAB1_FL905. Since the fluorescence intensity of pAB1_FL905 is dependent on its supercoiling status, pAB1_FL905 is a powerful tool to study DNA topology and topoisomerases by FRET. pAB1_FL905 can also be developed into rapid and efficient high-throughput screening assays to identify inhibitors that target various DNA topoisomerases.

Highlights

  • DNA supercoiling is a fundamental property of chromosomal DNA and plays critical roles in many essential DNA transactions, such as transcription, DNA replication, and recombination[1,2]

  • We describe a method to produce a type of fluorescently labeled circular DNA molecules with high yields to study DNA topology and topoisomerases by fluorescence resonance energy transfer (FRET)

  • As demonstrated previously[7,8,9], (-) supercoiling induces localized DNA conformation transitions, such as cruciform formation of inverted repeat sequences. These topology-dependent, structural isomerizations could be used to gauge the superhelicity of the DNA molecules

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Summary

Introduction

DNA supercoiling is a fundamental property of chromosomal DNA and plays critical roles in many essential DNA transactions, such as transcription, DNA replication, and recombination[1,2]. We describe a method to produce a type of fluorescently labeled circular DNA molecules with high yields to study DNA topology and topoisomerases by fluorescence resonance energy transfer (FRET). Similar to pAB1_FL905, the fluorescence intensity of rx pAB1_FL919, pAB1_FL920, and pAB1_ FL924 is significantly higher than that of the sc DNA molecules (Figures S4 and S5).

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