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The cell-surface proteoglycan Dally regulates Wingless signalling in Drosophila

  • Manabu Tsuda
  • , Keisuke Kamimura
  • , Hiroshi Nakato
  • , Michael Archer
  • , William Staatz
  • , Bethany Fox
  • , Melanie Humphrey
  • , Sara Olson
  • , Tracy Futch
  • , Vesna Kaluza
  • , Esther Siegfried
  • , Lynn Stam
  • , Scott B. Selleck

Research output: Contribution to journalArticlepeer-review

Abstract

Wingless (Wg) is a member of the Wnt family of growth factors, secreted proteins that control proliferation and differentiation during development. Studies in Drosophila have shown that responses to Wg require cell-surface heparan sulphate, a glycosaminoglycan component of proteoglycans. These findings suggest that a cell-surface proteoglycan is a component of a Wg/Wnt receptor complex. We demonstrate here that the protein encoded by the division abnormally delayed (dally) gene is a cell-surface, heparan-sulphate- modified proteoglycan, dally partial loss-of-function mutations compromise Wg-directed events, and disruption of dally function with RNA interference produces phenotypes comparable to those found with RNA interference of wg or frizzled (fz)/Dfz2 (ref. 7). Ectopic expression of Dally potentiates Wg signalling without altering levels of Wg and can rescue a wg partial loss- of-function mutant. We also show that dally, a regulator of Decapentaplegic (Dpp) signalling during post-embryonic development, has tissue-specific effects on Wg and Dpp signalling. Daily can therefore differentially influence signalling mediated by two growth factors, and may form a regulatory component of both Wg and Dpp receptor complexes.

Original languageEnglish (US)
Pages (from-to)276-280
Number of pages5
JournalNature
Volume400
Issue number6741
DOIs
StatePublished - Jul 15 1999

All Science Journal Classification (ASJC) codes

  • General

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