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PMID: 11395778 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

A freely diffusible form of Sonic hedgehog mediates long-range signalling.

Nature ·Vol. 411 ·No. 6838 ·2001-06-07 ·Pages 716-20

Zeng X, Goetz JA, Suber LM, Scott WJ, Schreiner CM, Robbins DJ

Abstract

The secreted protein Sonic hedgehog (Shh) exerts many of its patterning effects through a combination of short- and long-range signalling. Three distinct mechanisms, which are not necessarily mutually exclusive, have been proposed to account for the long-range effects of Shh: simple diffusion of Shh, a relay mechanism in which Shh activates secondary signals, and direct delivery of Shh through cytoplasmic extensions, termed cytonemes. Although there is much data (using soluble recombinant Shh (ShhN)) to support the simple diffusion model of long-range Shh signalling, there has been little evidence to date for a native form of Shh that is freely diffusible and not membrane-associated. Here we provide evidence for a freely diffusible form of Shh (s-ShhNp) that is cholesterol modified, multimeric and biologically potent. We further demonstrate that the availability of s-ShhNp is regulated by two functional antagonists of the Shh pathway, Patched (Ptc) and Hedgehog-interacting protein (Hip). Finally, we show a gradient of s-ShhNp across the anterior-posterior axis of the chick limb, demonstrating the physiological relevance of s-ShhNp.

MeSH Terms
Animals Carrier Proteins/metabolism Cell Line Chick Embryo Cholesterol/metabolism Gene Expression Regulation Genes, Reporter Hedgehog Proteins Limb Buds Membrane Glycoproteins/metabolism Membrane Proteins/metabolism Patched Receptors Proteins/metabolism Receptors, Cell Surface Signal Transduction Solubility Trans-Activators Transfection
Chemicals
Carrier Proteins Hedgehog Proteins Membrane Glycoproteins Membrane Proteins Patched Receptors Proteins Receptors, Cell Surface Trans-Activators Cholesterol
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Zeng X
Department of Molecular Genetics, Biochemistry and Microbiology, University of Cincinnati College of Medicine, 231 Albert Sabin Way, Cincinnati, Ohio 45267, USA.
Goetz J A
Suber L M
Scott W J
Schreiner C M
Robbins D J
Article Info
Journal
Nature
Abbr.
Nature
ISSN
0028-0836
Published
2001-06-07
Pages
716-20
Language
English
Region
England
NLM ID
0410462
Subset
IM
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