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Molecular cloning and expression of cDNA for human RNase H.

We have cloned, expressed, and purified to electrophoretic homogeneity a human RNase H. The enzyme has a molecular weight of 32 kDa, is Mg2+ dependent, and is inhibited by Mn2+ and N-ethylmaleimide. Its molecular weight and cleavage characteristics are consistent with type 2 human RNase H. The human RNase H we have cloned is highly homologous to Escherichia coli RNase HI (33.6% amino acid identity) and to other RNase H enzymes homologous to E. coli RNase HI. The enzyme is encoded by a single gene that is at least 10 kb in length and is expressed ubiquitously in human cells and tissues.[1]

References

  1. Molecular cloning and expression of cDNA for human RNase H. Wu, H., Lima, W.F., Crooke, S.T. Antisense Nucleic Acid Drug Dev. (1998) [Pubmed]
 
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