Abstract

RNase H1 from Escherichia coli cleaves single strand RNA extending 3' from an RNA-DNA duplex. Substrates consisting of a 25-mer RNA annealed to complementary DNA ranging in length from 9-17 nucleotides were designed to create overhanging single strand RNA regions extending 5' and 3' from the RNA-DNA duplex. Digestion of single strand RNA was observed exclusively within the 3' overhang region and not the 5' overhang region. RNase H digestion of the 3' overhang region resulted in digestion products with 5'-phosphate and 3'-hydroxyl termini. The number of single strand RNA residues cleaved by RNase H is influenced by the sequence of the single strand RNA immediately adjacent to the RNA-DNA duplex and appears to be a function of the stacking properties of the RNA residues adjacent to the RNA-DNA duplex. RNase H digestion of the 3' overhang region was not observed for a substrate that contained a 2'-methoxy antisense strand. The introduction of 3 deoxynucleotides at the 5' terminus of the 2'-methoxy antisense oligonucleotide resulted in cleavage. These results offer additional insights into the binding directionality of RNase H with respect to the heteroduplex substrate.

Highlights

  • RNase H1 from Escherichia coli is perhaps the best characterized isotype of this family of enzymes

  • Kinetic analyses of substrates containing RNA duplexed with chimeric oligonucleotides composed of a mixture of deoxy- and 2Ј-modified nucleotides demonstrated that the rate of cleavage was a function of the length of the deoxy portion of the chimeric oligonucleotide, i.e. the cleavage rate decreased with a diminishing number of contiguous deoxynucleotides, and complete loss in activity was observed for chimeric oligonucleotides containing less than 4 contiguous deoxynucleotides [6, 7]

  • In this communication we report that E. coli RNase H1 can cleave single strand RNA extending 3Ј from an RNA-DNA duplex

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Summary

Introduction

RNase H1 from Escherichia coli is perhaps the best characterized isotype of this family of enzymes. The greatest number of single strand RNA cleavage sites was observed for the substrate containing the string of three purines within the single strand region immediately adjacent to the heteroduplex (substrate 6, Fig. 1).

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