論文

査読有り
1999年7月

The cell-surface proteoglycan Dally regulates Wingless signalling in Drosophila

NATURE
  • M Tsuda
  • K Kamimura
  • H Nakato
  • M Archer
  • W Staatz
  • B Fox
  • M Humphrey
  • S Olson
  • T Futch
  • Kaluza, V
  • E Siegfried
  • L Stam
  • SB Selleck
  • 全て表示

400
6741
開始ページ
276
終了ページ
280
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1038/22336
出版者・発行元
MACMILLAN MAGAZINES LTD

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(1-4). 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(5,6). dally partial loss-of-function mutations compromise Wg-directed events, and disruption of daily function with RNA interference produces phenotypes comparable to those found with RNA interference of wg or frizzled (fz)/Dfz2 (ref. 7). Ectopic expression of Daily 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 (DFP) 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.

リンク情報
DOI
https://doi.org/10.1038/22336
CiNii Articles
http://ci.nii.ac.jp/naid/80011201652
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/10421371
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000081503800047&DestApp=WOS_CPL
ID情報
  • DOI : 10.1038/22336
  • ISSN : 0028-0836
  • CiNii Articles ID : 80011201652
  • PubMed ID : 10421371
  • Web of Science ID : WOS:000081503800047

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