Formation of mRNP granules in Toxoplasma gondii during the lytic cycle

Mol Biochem Parasitol. 2021 Mar:242:111349. doi: 10.1016/j.molbiopara.2020.111349. Epub 2020 Dec 28.

Abstract

Two poly(A) binding proteins (PABPs) of Toxoplasma gondii, were identified and characterized. They were named TgPABPC and TgPABPN as they were found to localize in the cytoplasm and nucleus respectively. TgPABPC, which colocalizes with mRNA granules, is therefore used as a cellular marker of mRNP granules. We detected that the formation of mRNP granules was independent of polymerized microtubules, and that the granules were distributed stochastically within the cytosol. Formation of mRNP granules was found to occur prior to parasite egress when a Ca2+ ionophore is used to induce egress. It was also found that maturation of mRNP granules could be described as a two-phase process. First, prior to host cell lysis, mRNP granules were formed rapidly within the cytosol. Second, the mRNP granule load was reduced within 10 min post egress. To investigate the link between translational state and mRNP granule formation, treatments with salubrinal, nutrient deprivation, and pH stress were used. While salubrinal induced granule formation in tachyzoites, nutrient starvation and pH stress showed no induction effect on mRNP granule formation. Interestingly, salubrinal treatment in bradyzoites did not induce RNP granule formation, thus suggesting that mRNP granule formation is not a ubiquitous response or directly related to translational repression. Instead, mRNP granule formation is likely a response to the rapid increase in non-translating RNA brought on by sudden changes in translational state.

Keywords: Invasion; Poly(A) binding protein; RNP granule; Stress; Toxoplasma gondii.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Calcium Ionophores / pharmacology
  • Cell Line
  • Cell Nucleus / metabolism
  • Cell Nucleus / ultrastructure
  • Cinnamates / pharmacology
  • Cytoplasmic Granules / metabolism*
  • Cytoplasmic Granules / ultrastructure
  • Fibroblasts / drug effects
  • Fibroblasts / parasitology
  • Fibroblasts / ultrastructure
  • Gene Expression Regulation
  • Humans
  • Hydrogen-Ion Concentration
  • Life Cycle Stages / genetics*
  • Microtubules / metabolism
  • Microtubules / ultrastructure
  • Poly(A)-Binding Proteins / genetics*
  • Poly(A)-Binding Proteins / metabolism
  • Protein Biosynthesis
  • Protein Isoforms / genetics
  • Protein Isoforms / metabolism
  • Protozoan Proteins / genetics*
  • Protozoan Proteins / metabolism
  • RNA, Protozoan / genetics
  • RNA, Protozoan / metabolism
  • Ribonucleoproteins / genetics*
  • Ribonucleoproteins / metabolism
  • Sequence Alignment
  • Sequence Homology, Amino Acid
  • Thiourea / analogs & derivatives
  • Thiourea / pharmacology
  • Toxoplasma / drug effects
  • Toxoplasma / genetics*
  • Toxoplasma / growth & development
  • Toxoplasma / ultrastructure

Substances

  • Calcium Ionophores
  • Cinnamates
  • Poly(A)-Binding Proteins
  • Protein Isoforms
  • Protozoan Proteins
  • RNA, Protozoan
  • Ribonucleoproteins
  • messenger ribonucleoprotein
  • salubrinal
  • Thiourea