Evidence for the Nucleo-Apical Shuttling of a Beta-Catenin Like Plasmodium falciparum Armadillo Repeat Containing Protein

PLoS One. 2016 Feb 1;11(2):e0148446. doi: 10.1371/journal.pone.0148446. eCollection 2016.

Abstract

Eukaryotic Armadillo (ARM) repeat proteins are multifaceted with prominent roles in cell-cell adhesion, cytoskeletal regulation and intracellular signaling among many others. One such ARM repeat containing protein, ARM Repeats Only (ARO), has recently been demonstrated in both Toxoplasma (TgARO) and Plasmodium (PfARO) parasites to be targeted to the rhoptries during the late asexual stages. TgARO has been implicated to play an important role in rhoptry positioning i.e. directing the rhoptry towards the apical end of the parasite. Here, we report for the first time that PfARO exhibits a DNA binding property and a dynamic sub-cellular localization between the nucleus (early schizont) and rhoptry (late schizont) during the different stages of the asexual blood-stage life cycle. PfARO possesses a putative nuclear export signal (NES) and the nucleo-apical shuttling was sensitive to Leptomycin B (LMB) suggesting that the nuclear export was mediated by CRM1. Importantly, PfARO specifically bound an A-T rich DNA sequence of the P. falciparum Gyrase A (PfgyrA) gene, suggesting that the DNA binding specificity of PfARO is likely due to the AT-richness of the probe. This is a novel functional characteristic that has not been reported previously for any P. falciparum ARM containing protein and suggests a putative role for PfARO in gene regulation. This study describes for the first time a conserved P. falciparum ARM repeat protein with a high degree of functional versatility.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antibodies, Protozoan / metabolism
  • Antibody Specificity / drug effects
  • Armadillo Domain Proteins / chemistry
  • Armadillo Domain Proteins / metabolism*
  • Biomarkers / metabolism
  • Cell Nucleus / drug effects
  • Cell Nucleus / metabolism*
  • Conserved Sequence
  • DNA / metabolism
  • Erythrocytes / drug effects
  • Erythrocytes / parasitology
  • Fatty Acids, Unsaturated / pharmacology
  • Fluorescent Antibody Technique
  • Humans
  • Life Cycle Stages / drug effects
  • Mass Spectrometry
  • Parasites / drug effects
  • Parasites / metabolism
  • Plasmodium falciparum / drug effects
  • Plasmodium falciparum / immunology
  • Plasmodium falciparum / metabolism*
  • Protein Binding / drug effects
  • Protein Transport / drug effects
  • Protozoan Proteins / chemistry
  • Protozoan Proteins / metabolism*
  • Recombinant Proteins / metabolism
  • Solubility
  • beta Catenin / metabolism*

Substances

  • Antibodies, Protozoan
  • Armadillo Domain Proteins
  • Biomarkers
  • Fatty Acids, Unsaturated
  • Protozoan Proteins
  • Recombinant Proteins
  • beta Catenin
  • DNA
  • leptomycin B

Grants and funding

This work was supported by the following grants of the Department of Biotechnology, Ministry of Science and Technology, Government of India: Program Support Grant to D.G. and V.S.C.; Ramalingaswami fellowship contingency grant to D.G.; as well as the UPEII grant from Jawaharlal Nehru University (JNU) to D.G. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.