TRF1 inhibits telomere C-strand DNA synthesis in vitro

Biochemistry. 2001 Feb 27;40(8):2426-32. doi: 10.1021/bi001871o.

Abstract

Human TTAGGG repeat-binding factor 1 (TRF1) is involved in the regulation of telomere length in vivo, but the mechanism of regulation remains largely undefined. We have developed an in vitro system for assessing the effect of TRF1 on DNA synthesis using purified proteins and synthetic DNA substrates. Results reveal that TRF1, when bound to telomeric duplex DNA, inhibits DNA synthesis catalyzed by DNA polymerase alpha/primase (pol alpha). Inhibition required that TRF1 be bound to duplex telomeric DNA as no effect of TRF1 was observed on nontelomeric, random DNA substrates. Inhibition was shown to be dependent on TRF1 concentration and the length of the telomeric duplex region of the DNA substrate. When bound in cis to telomeric duplex DNA, TRF1 was also capable of inhibiting pol alpha-catalyzed DNA synthesis on nontelomeric DNA sequences from positions both upstream and downstream of the extending polymerase. Inhibition of DNA synthesis was shown to be specific for TRF1 but not necessarily for the DNA polymerase used in the extension reaction. In a series of control experiments, we assessed T7 DNA polymerase-catalyzed synthesis on a DNA template containing tandem gal4 operators. In these experiments, the addition of the purified Gal4-DNA binding domain (Gal4-DBD) protein has no effect on the ability of T7 polymerase to copy the DNA template. Interestingly, TRF1 inhibition was observed on telomeric DNA substrates using T7 DNA polymerase. These results suggest that TRF1, when bound to duplex telomeric DNA, serves to block extension by DNA polymerases. These results are discussed with respect to the role of TRF1 in telomere length regulation.

Publication types

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

MeSH terms

  • Animals
  • Base Sequence
  • Binding, Competitive / genetics
  • Catalysis
  • DNA / antagonists & inhibitors*
  • DNA / biosynthesis*
  • DNA / chemical synthesis
  • DNA / metabolism
  • DNA Polymerase I / metabolism
  • DNA Polymerase I / physiology
  • DNA Primase / metabolism
  • DNA Primers / metabolism
  • DNA Replication / genetics*
  • DNA-Binding Proteins / genetics*
  • DNA-Binding Proteins / metabolism
  • Molecular Sequence Data
  • Nucleic Acid Heteroduplexes / genetics
  • Nucleic Acid Heteroduplexes / metabolism
  • Protein Binding / genetics
  • Recombinant Fusion Proteins / metabolism
  • Recombinant Fusion Proteins / pharmacology*
  • Repetitive Sequences, Nucleic Acid
  • Spodoptera / genetics
  • Substrate Specificity / genetics
  • Telomere / genetics*
  • Telomeric Repeat Binding Protein 1

Substances

  • DNA Primers
  • DNA-Binding Proteins
  • Nucleic Acid Heteroduplexes
  • Recombinant Fusion Proteins
  • Telomeric Repeat Binding Protein 1
  • DNA
  • DNA Primase
  • DNA Polymerase I