Single molecule analysis of Trypanosoma brucei DNA replication dynamics

Nucleic Acids Res. 2015 Mar 11;43(5):2655-65. doi: 10.1093/nar/gku1389. Epub 2015 Feb 17.

Abstract

Eukaryotic genome duplication relies on origins of replication, distributed over multiple chromosomes, to initiate DNA replication. A recent genome-wide analysis of Trypanosoma brucei, the etiological agent of sleeping sickness, localized its replication origins to the boundaries of multigenic transcription units. To better understand genomic replication in this organism, we examined replication by single molecule analysis of replicated DNA. We determined the average speed of replication forks of procyclic and bloodstream form cells and we found that T. brucei DNA replication rate is similar to rates seen in other eukaryotes. We also analyzed the replication dynamics of a central region of chromosome 1 in procyclic forms. We present evidence for replication terminating within the central part of the chromosome and thus emanating from both sides, suggesting a previously unmapped origin toward the 5' extremity of chromosome 1. Also, termination is not at a fixed location in chromosome 1, but is rather variable. Importantly, we found a replication origin located near an ORC1/CDC6 binding site that is detected after replicative stress induced by hydroxyurea treatment, suggesting it may be a dormant origin activated in response to replicative stress. Collectively, our findings support the existence of more replication origins in T. brucei than previously appreciated.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Cycle Proteins / genetics
  • Cell Cycle Proteins / metabolism
  • Chromosomes / genetics
  • DNA Replication / drug effects
  • DNA Replication / genetics*
  • DNA, Protozoan / genetics*
  • Flow Cytometry
  • Genome, Protozoan / genetics
  • Hydroxyurea / pharmacology
  • Kinetics
  • Life Cycle Stages / genetics
  • Molecular Biology / methods*
  • Nucleic Acid Synthesis Inhibitors / pharmacology
  • Origin Recognition Complex / genetics
  • Origin Recognition Complex / metabolism
  • Polymerase Chain Reaction
  • Protozoan Proteins / genetics
  • Protozoan Proteins / metabolism
  • Replication Origin / genetics*
  • Time Factors
  • Trypanosoma brucei brucei / drug effects
  • Trypanosoma brucei brucei / genetics*
  • Trypanosoma brucei brucei / growth & development

Substances

  • Cell Cycle Proteins
  • DNA, Protozoan
  • Nucleic Acid Synthesis Inhibitors
  • Origin Recognition Complex
  • Protozoan Proteins
  • Hydroxyurea