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Science 11 October 1996: Vol. 274. no. 5285, pp. 255 - 259 DOI: 10.1126/science.274.5285.255
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Reports
Cholesterol Modification of Hedgehog Signaling Proteins in Animal
Development
Jeffery A. Porter,
Keith E. Young,
Philip
A. Beachy
*
Hedgehog (Hh) proteins comprise a family of secreted signaling
molecules essential for patterning a variety of structures in animal
embryogenesis. During biosynthesis, Hh undergoes an autocleavage
reaction, mediated by its carboxyl-terminal domain, that produces a
lipid-modified amino-terminal fragment responsible for all known Hh
signaling activity. Here it is reported that cholesterol is the
lipophilic moiety covalently attached to the amino-terminal signaling
domain during autoprocessing and that the carboxyl-terminal domain acts
as an intramolecular cholesterol transferase. This use of cholesterol
to modify embryonic signaling proteins may account for some of the
effects of perturbed cholesterol biosynthesis on animal development.
Howard Hughes Medical Institute, Department of Molecular Biology
and Genetics, Johns Hopkins School of Medicine, Baltimore, MD 21205, USA.
*
To whom correspondence should be addressed.
Read the Full Text
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- Association of Multiple Developmental Defects and Embryonic Lethality with Loss of Microsomal NADPH-Cytochrome P450 Oxidoreductase.
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- Distinct roles of Central missing and Dispatched in sending the Hedgehog signal.
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Development
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- Apoptosis-induced release of mature sterol regulatory element-binding proteins activates sterol-responsive genes.
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J. Lipid Res.
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- Hedgehog Signaling: A Tale of Two Lipids.
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Science
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- Regulation of Mitochondrial Carbamoyl-phosphate Synthetase 1 Activity by Active Site Fatty Acylation.
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- Fat Hedgehogs, Slower or Richer?.
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Sci. STKE
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- Inborn errors of metabolism: A cause of abnormal brain development.
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Neurology
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- The hedgehog pathway and basal cell carcinomas.
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Hum. Mol. Genet.
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- A Caveolin Dominant Negative Mutant Associates with Lipid Bodies and Induces Intracellular Cholesterol Imbalance.
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- Cholesterol sulfate stimulates involucrin transcription in keratinocytes by increasing Fra-1, Fra-2, and Jun D.
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