The Integrator complex desensitizes cellular response to TGF-β/BMP signaling

Cell Rep. 2023 Jan 31;42(1):112007. doi: 10.1016/j.celrep.2023.112007. Epub 2023 Jan 14.

Abstract

Maintenance of stem cells requires the concerted actions of niche-derived signals and stem cell-intrinsic factors. Although Decapentaplegic (Dpp), a Drosophila bone morphogenetic protein (BMP) molecule, can act as a long-range morphogen, its function is spatially limited to the germline stem cell niche in the germarium. We show here that Integrator, a complex known to be involved in RNA polymerase II (RNAPII)-mediated transcriptional regulation in the nucleus, promotes germline differentiation by restricting niche-derived Dpp/BMP activity in the cytoplasm. Further results show that Integrator works in various developmental contexts to desensitize the cellular response to Dpp/BMP signaling during Drosophila development. Mechanistically, our results show that Integrator forms a multi-subunit complex with the type I receptor Thickveins (Tkv) and other Dpp/BMP signaling components and acts in a negative feedback loop to promote Tkv turnover independent of its transcriptional activity. Similarly, human Integrator subunits bind transforming growth factor β (TGF-β)/BMP signaling components and antagonize their activity, suggesting a conserved role of Integrator across metazoans.

Keywords: CP: Cell biology; CP: Stem cell research; Dpp/BMP signaling; Drosophila; E3 ubiquitin ligase; I-Smad; Integrator; Smurf; TGF-β/BMP signaling; germline stem cells; stem cell niche; stem cells.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bone Morphogenetic Proteins / metabolism
  • Cell Differentiation / physiology
  • Drosophila / metabolism
  • Drosophila Proteins* / genetics
  • Drosophila Proteins* / metabolism
  • Humans
  • Protein Serine-Threonine Kinases / metabolism
  • Receptors, Cell Surface / metabolism
  • Signal Transduction / physiology
  • Transforming Growth Factor beta* / metabolism

Substances

  • Transforming Growth Factor beta
  • Drosophila Proteins
  • Bone Morphogenetic Proteins
  • dpp protein, Drosophila
  • tkv protein, Drosophila
  • Receptors, Cell Surface
  • Protein Serine-Threonine Kinases