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Cited by 194

The DOI matches its Crossref record; 2 of the 2 references it cites were found in a registry or an index.

Defects in glucuronate biosynthesis disrupt Wingless signaling in Drosophila

Open access
Haerry, Theodor E., Heslip, Tim R., Marsh, J. Lawrence, O’Connor, Michael B.·1997·Development

Abstract

In vitro experiments suggest that glycosaminoglycans (GAGs) and the proteins to which they are attached (proteoglycans) are important for modulating growth factor signaling. However, in vivo evidence to support this view has been lacking, in part because mutations that disrupt the production of GAG polymers and the core proteins have not been available. Here we describe the identification and characterization of Drosophila mutants in the suppenkasper (ska) gene. The ska gene encodes UDP-glucose dehydrogenase which produces glucuronic acid, an essential component for the synthesis of heparan and chondroitin sulfate. ska mutants fail to put heparan side chains on proteoglycans such as Syndecan. Surprisingly, mutant embryos produced by germ-line clones of this general metabolic gene exhibit embryonic cuticle phenotypes strikingly similar to those that result from loss-of-function mutations in genes of the Wingless (Wg) signaling pathway. Zygotic loss of ska leads to reduced growth of imaginal discs and pattern defects similar to wg mutants. In addition, genetic interactions of ska with wg and dishevelled mutants are observed. These data demonstrate the importance of proteoglycans and GAGs in Wg signaling in vivo and suggest that Wnt-like growth factors may be particularly sensitive to perturbations of GAG biosynthesis.

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Crossref · 10.1242/dev.124.16.3055

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Metadata

Authors
Haerry, T. E., Heslip, T. R., Marsh, J. L., & O’Connor, M. B.
Venue
Development
Published
1997-08-15
Volume
124
Issue
16
Pages
3055-3064
ISSN
  • 0950-1991 (ISSN-L)
  • 1477-9129
OpenAlex
W2169483492
Cited by
194
References
2
FWCI
7.37
Type
journal article
Language
en
Open access
green

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