Trypanosoma cruzi Fibrillarins: Two paralogous proteins with non-identical signals for nuclear transport

Biochem Biophys Res Commun. 2023 Nov 19:682:274-280. doi: 10.1016/j.bbrc.2023.10.025. Epub 2023 Oct 7.

Abstract

Trypanosoma cruzi is a parasitic protozoa causative of Chagas disease. As part of our interest in studying the basic biology of this microorganism, this work reports our observations related to the characterization of motifs and structural domains present in two fibrillarin isoforms (TcFib1 and TcFib2) that were found to be necessary for the nuclear targeting of these nucleolar proteins. Previous characterization of these proteins indicated that they share 68.67% of identical amino acids and are both expressed as nucleolar proteins in T. cruzi epimastigotes. Using an approach based on the transfection of recombinant genes encoding fluorescent fibrillarin-EGFP fusion proteins, this study found evidence for the presence of 4 motifs or protein domains that help target these proteins to the nucleus: The GAR domain and carboxyl terminus in both TcFibs, as well as two lysines and a computationally predicted cNLS in TcFib1. As a distinctive feature, the GAR domain of TcFib2 proved to be essential for the nuclear localization of this protein paralog. Such a difference between TcFib1 and Tcfib2 nuclear localization signals can be explained as the presence of two partially related nuclear import pathways for the two fibrillarin homologues in this organism.

Keywords: Nucleolus; Nucleus; Protozoa; Trypanosomatid.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Active Transport, Cell Nucleus
  • Cell Nucleolus / metabolism
  • Chagas Disease*
  • Chromosomal Proteins, Non-Histone / metabolism
  • Humans
  • Nuclear Localization Signals / genetics
  • Nuclear Localization Signals / metabolism
  • Nuclear Proteins / genetics
  • Nuclear Proteins / metabolism
  • Trypanosoma cruzi* / genetics
  • Trypanosoma cruzi* / metabolism

Substances

  • fibrillarin
  • Chromosomal Proteins, Non-Histone
  • Nuclear Localization Signals
  • Nuclear Proteins