Separation of newly-synthesized RNA by organomercurial agarose affinity chromatography

J Biochem. 1977 May;81(5):1247-52.

Abstract

Mouse myeloma cells, MOPC-31C, were incubated in the presence of 2-thiouridine and newly-synthesized RNA which appeared to contain 2-thioUMP as a constituent was separated from preexisting RNA by affinity chromatography using organomercurial agarose as a support. Both pH and salt concentration greatly affected the specific adsorption of the newly-synthesized RNA on the column. Under optimal conditions the rate of adsorption of the newly-synthesized RNA on the column was proportional to the logarithmic concentration of 2-thiouridine in the culture medium. Furthermore, at a given concentration of 2-thiouridine in the medium, a shorter incubation period caused a reduction of the rate of RNA adsorption on the column. The molecular size distributions of both total RNA and the adsorbed fraction, synthesized during 30 min in the presence of 2-thiouridine, were similar to that of RNA synthesized in the absence of the drug.

MeSH terms

  • Cell Line
  • Chromatography, Affinity / methods
  • Hydrogen-Ion Concentration
  • Kinetics
  • Organomercury Compounds
  • Osmolar Concentration
  • RNA, Neoplasm* / biosynthesis
  • RNA, Neoplasm* / isolation & purification
  • Sodium Chloride
  • Thiouridine / metabolism

Substances

  • Organomercury Compounds
  • RNA, Neoplasm
  • Thiouridine
  • Sodium Chloride