Promyelocytic leukemia nuclear body-like structures can assemble in mouse oocytes

Biol Open. 2022 Jun 15;11(6):bio059130. doi: 10.1242/bio.059130. Epub 2022 Jun 6.

Abstract

Promyelocytic leukemia (PML) nuclear bodies (PML-NBs), a class of membrane-less cellular organelles, participate in various biological activities. PML-NBs are known as the core-shell-type nuclear body, harboring 'client' proteins in their core. Although multiple membrane-less organelles work in the oocyte nucleus, PML-NBs have been predicted to be absent from oocytes. Here, we show that some well-known PML clients (but not endogenous PML) co-localized with small ubiquitin-related modifier (SUMO) protein in the nucleolus and peri-centromeric heterochromatin of maturing oocytes. In oocytes devoid of PML-NBs, endogenous PML protein localized in the vicinity of chromatin. During and after meiotic resumption, PML co-localized with SUMO gathering around chromosomes. To examine the benefit of the PML-NB-free intranuclear milieu in oocytes, we deliberately assembled PML-NBs by microinjecting human PML-encoding plasmids into oocytes. Under conditions of limited SUMO availability, assembled PML-NBs tended to cluster. Upon proteotoxic stress, SUMO delocalized from peri-centromeric heterochromatin and co-localized with SC35 (a marker of nuclear speckles)-positive large compartments, which was disturbed by pre-assembled PML-NBs. These observations suggest that the PML-NB-free intranuclear environment helps reserve SUMO for emergent responses by redirecting the flux of SUMO otherwise needed to maintain PML-NB dynamics.

Keywords: Clients; Membrane-less organelle; Oocyte; PML-NBs; Proteotoxic stress; SUMO.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Heterochromatin* / genetics
  • Humans
  • Leukemia*
  • Mice
  • Nuclear Bodies
  • Oocytes / metabolism
  • Promyelocytic Leukemia Protein / genetics
  • Promyelocytic Leukemia Protein / metabolism
  • Small Ubiquitin-Related Modifier Proteins / metabolism

Substances

  • Heterochromatin
  • Promyelocytic Leukemia Protein
  • Small Ubiquitin-Related Modifier Proteins