Efficient N-tailing of blunt DNA ends by Moloney murine leukemia virus reverse transcriptase

Sci Rep. 2017 Feb 2:7:41769. doi: 10.1038/srep41769.

Abstract

Moloney murine leukemia virus reverse transcriptase (MMLV-RT) is a widely used enzyme for cDNA synthesis. Here we show that MMLV-RT has a strong template-independent polymerase activity using blunt DNA ends as substrate that generates 3' overhangs of A, C, G, or T. Nucleotides were appended efficiently in the order A > G > T > C, and tail lengths varied from 4 to 5, 2 to 7, 2 to 4, and 2 to 3 for A, C, G, and T, respectively. The activity was so strong that nearly all our test DNA ends were appended with at least one A, C, G, or T. The N-tailing activity of MMLV-RT was enhanced in the presence of Mn2+, and the G-, C-, and T-tailing activities were further enhanced by dCMP, dGMP, and dAMP, respectively. This is the first report of an enzymatic activity that almost thoroughly appends two or more As, or one or more Cs, Gs, or Ts to the 3' end of double-stranded DNA, which would enable exhaustive analysis of DNA samples. The N-tailing activity of MMLV-RT is potentially useful in many biotechnological applications.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • DNA / genetics
  • DNA / metabolism*
  • DNA, Complementary / genetics
  • DNA, Complementary / metabolism
  • Enzyme Activation
  • Mice
  • Moloney murine leukemia virus / genetics
  • Moloney murine leukemia virus / physiology*
  • RNA-Directed DNA Polymerase / metabolism*
  • Reverse Transcription*
  • Templates, Genetic

Substances

  • DNA, Complementary
  • DNA
  • RNA-Directed DNA Polymerase