Asymmetric inheritance of cytoophidia could contribute to determine cell fate and plasticity: The onset of alternative differentiation patterns in daughter cells may rely on the acquisition of either CTPS or IMPDH cytoophidia: The onset of alternative differentiation patterns in daughter cells may rely on the acquisition of either CTPS or IMPDH cytoophidia

Bioessays. 2022 Dec;44(12):e2200128. doi: 10.1002/bies.202200128. Epub 2022 Oct 9.

Abstract

Two enzymes involved in the synthesis of pyrimidine and purine nucleotides, CTP synthase (CTPS) and IMP dehydrogenase (IMPDH), can assemble into a single or very few large filaments called rods and rings (RR) or cytoophidia. Most recently, asymmetric cytoplasmic distribution of organelles during cell division has been described as a decisive event in hematopoietic stem cell fate. We propose that cytoophidia, which could be considered as membrane-less organelles, may also be distributed asymmetrically during mammalian cell division as previously described for Schizosaccharomyces pombe. Furthermore, because each type of nucleotide intervenes in distinct processes (e.g., membrane synthesis, glycosylation, and G protein-signaling), alterations in the rate of synthesis of specific nucleotide types could influence cell differentiation in multiple ways. Therefore, we hypothesize that whether a daughter cell inherits or not CTPS or IMPDH filaments determines its fate and that this asymmetric inheritance, together with the dynamic nature of these structures enables plasticity in a cell population.

Keywords: CTPS; IMPDH; asymmetric division; cytoophidia; differentiation; plasticity; ribonucleotides.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Carbon-Nitrogen Ligases* / genetics
  • Carbon-Nitrogen Ligases* / metabolism
  • Cell Differentiation
  • IMP Dehydrogenase / metabolism
  • Mammals / metabolism
  • Nucleotides / metabolism
  • Schizosaccharomyces* / genetics

Substances

  • CTP synthetase
  • IMP Dehydrogenase
  • Carbon-Nitrogen Ligases
  • Nucleotides