A dynamic interplay between chitin synthase and the proteins Expansion/Rebuf reveals that chitin polymerisation and translocation are uncoupled in Drosophila

PLoS Biol. 2023 Jan 23;21(1):e3001978. doi: 10.1371/journal.pbio.3001978. eCollection 2023 Jan.

Abstract

Chitin is a highly abundant polymer in nature and a principal component of apical extracellular matrices in insects. In addition, chitin has proved to be an excellent biomaterial with multiple applications. In spite of its importance, the molecular mechanisms of chitin biosynthesis and chitin structural diversity are not fully elucidated yet. To investigate these issues, we use Drosophila as a model. We previously showed that chitin deposition in ectodermal tissues requires the concomitant activities of the chitin synthase enzyme Kkv and the functionally interchangeable proteins Exp and Reb. Exp/Reb are conserved proteins, but their mechanism of activity during chitin deposition has not been elucidated yet. Here, we carry out a cellular and molecular analysis of chitin deposition, and we show that chitin polymerisation and chitin translocation to the extracellular space are uncoupled. We find that Kkv activity in chitin translocation, but not in polymerisation, requires the activity of Exp/Reb, and in particular of its conserved Nα-MH2 domain. The activity of Kkv in chitin polymerisation and translocation correlate with Kkv subcellular localisation, and in absence of Kkv-mediated extracellular chitin deposition, chitin accumulates intracellularly as membrane-less punctae. Unexpectedly, we find that although Kkv and Exp/Reb display largely complementary patterns at the apical domain, Exp/Reb activity nonetheless regulates the topological distribution of Kkv at the apical membrane. We propose a model in which Exp/Reb regulate the organisation of Kkv complexes at the apical membrane, which, in turn, regulates the function of Kkv in extracellular chitin translocation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Chitin Synthase / genetics
  • Chitin Synthase / metabolism
  • Chitin* / chemistry
  • Chitin* / metabolism
  • Drosophila Proteins* / genetics
  • Drosophila Proteins* / metabolism
  • Drosophila* / metabolism
  • Mutation
  • Smad Proteins* / metabolism

Substances

  • Chitin
  • Chitin Synthase
  • Drosophila Proteins
  • kkv protein, Drosophila
  • exp protein, Drosophila
  • Smad Proteins

Grants and funding

This work was supported by the Spanish Ministerio de Ciencia e Innovación (FPI Fellowship BES-2016-076723 to EDG and BFU-2015-68098-P and PGC2018-098449-B-I00 grants to ML). PG is a researcher in Prof. Jordi Casanova's lab funded by Spanish Ministerio de Ciencia e Innovación (PGC2018-094254-B-100 grant) and the CERCA Program of the Catalan Government. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.