Isolation and characterization of an RNA ligase from HeLa cells

Proc Natl Acad Sci U S A. 1985 Feb;82(3):684-8. doi: 10.1073/pnas.82.3.684.

Abstract

An RNA ligase has been purified from HeLa cells, which catalyzes the intra- and intermolecular ligation of linear RNA substrates possessing 5'-hydroxyl and 2',3'-cyclic phosphate termini in the presence of ATP or dATP. In this reaction, the 2',3'-cyclic phosphate is incorporated into a 3'-5'-phosphodiester bond, in agreement with the findings of Filipowicz et al. [Filipowicz, W., Konarska, M., Gross, H. J. & Shatkin, A. J. (1983) Nucleic Acids Res. 11, 1405-1418]. The activity of the purified enzyme is dependent on the addition of ATP or dATP, a divalent cation (Mg2+), and 5'-hydroxyl, 2',3'-cyclic phosphate-terminated RNA substrates. No ligation occurs with the substrates OH(Up)10G(3')p or OH(Up)10G(2')p or with 5'-phosphate, 2',3'-cyclic phosphate-terminated oligoribonucleotides.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adenosine Triphosphate / metabolism
  • HeLa Cells / enzymology*
  • Humans
  • Kinetics
  • Magnesium / metabolism
  • Polynucleotide Ligases / isolation & purification*
  • RNA Ligase (ATP) / isolation & purification*
  • RNA Splicing
  • Substrate Specificity

Substances

  • Adenosine Triphosphate
  • Polynucleotide Ligases
  • RNA Ligase (ATP)
  • Magnesium