Hecw controls oogenesis and neuronal homeostasis by promoting the liquid state of ribonucleoprotein particles

Nat Commun. 2021 Sep 16;12(1):5488. doi: 10.1038/s41467-021-25809-8.

Abstract

Specialised ribonucleoprotein (RNP) granules are a hallmark of polarized cells, like neurons and germ cells. Among their main functions is the spatial and temporal modulation of the activity of specific mRNA transcripts that allow specification of primary embryonic axes. While RNPs composition and role are well established, their regulation is poorly defined. Here, we demonstrate that Hecw, a newly identified Drosophila ubiquitin ligase, is a key modulator of RNPs in oogenesis and neurons. Hecw depletion leads to the formation of enlarged granules that transition from a liquid to a gel-like state. Loss of Hecw activity results in defective oogenesis, premature aging and climbing defects associated with neuronal loss. At the molecular level, reduced ubiquitination of the Fmrp impairs its translational repressor activity, resulting in altered Orb expression in nurse cells and Profilin in neurons.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cytoplasmic Granules / metabolism
  • Drosophila Proteins / genetics*
  • Drosophila Proteins / metabolism
  • Drosophila melanogaster / cytology
  • Drosophila melanogaster / genetics*
  • Drosophila melanogaster / growth & development
  • Drosophila melanogaster / metabolism
  • Embryo, Nonmammalian
  • Fragile X Mental Retardation Protein / genetics
  • Fragile X Mental Retardation Protein / metabolism
  • Gene Expression Regulation, Developmental*
  • Homeostasis / genetics
  • Longevity / genetics
  • Neurogenesis / genetics*
  • Neurons / cytology
  • Neurons / metabolism
  • Oocytes / cytology
  • Oocytes / metabolism
  • Oogenesis / genetics*
  • Phase Transition
  • Profilins / genetics
  • Profilins / metabolism
  • Protein Biosynthesis
  • Protein Processing, Post-Translational
  • RNA-Binding Proteins / genetics
  • RNA-Binding Proteins / metabolism
  • Ribonucleoproteins / genetics*
  • Ribonucleoproteins / metabolism
  • Ubiquitin-Protein Ligases / genetics*
  • Ubiquitin-Protein Ligases / metabolism
  • Ubiquitination

Substances

  • Drosophila Proteins
  • Profilins
  • RNA-Binding Proteins
  • Ribonucleoproteins
  • orb protein, Drosophila
  • Fragile X Mental Retardation Protein
  • Ubiquitin-Protein Ligases