TGFß/activin-dependent activation of Torso controls the timing of the metamorphic transition in the red flour beetle Tribolium castaneum

PLoS Genet. 2023 Nov 27;19(11):e1010897. doi: 10.1371/journal.pgen.1010897. eCollection 2023 Nov.

Abstract

Understanding the mechanisms governing body size attainment during animal development is of paramount importance in biology. In insects, a crucial phase in determining body size occurs at the larva-pupa transition, marking the end of the larval growth period. Central to this process is the attainment of the threshold size (TS), a critical developmental checkpoint that must be reached before the larva can undergo metamorphosis. However, the intricate molecular mechanisms by which the TS orchestrates this transition remain poor understood. In this study, we investigate the role of the interaction between the Torso and TGFß/activin signaling pathways in regulating metamorphic timing in the red flour beetle, Tribolium castaneum. Our results show that Torso signaling is required specifically during the last larval instar and that its activation is mediated not only by the prothoracicotropic hormone (Tc-Ptth) but also by Trunk (Tc-Trk), another ligand of the Tc-Torso receptor. Interestingly, we show that while Tc-Torso activation by Tc-Ptth determines the onset of metamorphosis, Tc-Trk promotes growth during the last larval stage. In addition, we found that the expression of Tc-torso correlates with the attainment of the TS and the decay of juvenile hormone (JH) levels, at the onset of the last larval instar. Notably, our data reveal that activation of TGFß/activin signaling pathway at the TS is responsible for repressing the JH synthesis and inducing Tc-torso expression, initiating metamorphosis. Altogether, these findings shed light on the pivotal involvement of the Ptth/Trunk/Torso and TGFß/activin signaling pathways as critical regulatory components orchestrating the TS-driven metamorphic initiation, offering valuable insights into the mechanisms underlying body size determination in insects.

MeSH terms

  • Animals
  • Gene Expression Regulation, Developmental
  • Insect Proteins* / genetics
  • Insect Proteins* / metabolism
  • Juvenile Hormones / genetics
  • Juvenile Hormones / metabolism
  • Larva / metabolism
  • Metamorphosis, Biological
  • Receptor Protein-Tyrosine Kinases* / metabolism
  • Tribolium* / growth & development
  • Tribolium* / metabolism

Substances

  • Insect Proteins
  • Juvenile Hormones
  • Receptor Protein-Tyrosine Kinases

Grants and funding

This project is supported by grants PGC2018-098427-B-I00 and PID2021-125661NB-I00 to D.M. and X.F-M. funded by MCIN/AEI/10.13039/501100011033 and by “ERDF A way of making Europe”. The project is supported also by grants 2017 SGR 1030 and 2021 SGR 00417 to D.M. and X.F-M funded by the Departament de Recerca i Universitats de la Generalitat de Catalunya. S.C. was a recipient of a Juan de la Cierva contract FJC2019-041549-I funded by MCIN/AEI /10.13039/501100011033. The funders play no role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript.