Source:http://linkedlifedata.com/resource/pubmed/id/15556637
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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
3
|
| pubmed:dateCreated |
2004-11-23
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| pubmed:abstractText |
The natural cofactor of phenylalanine hydroxylase (PAH), tetrahydrobiopterin (BH4), regulates the enzyme activity as well as being essential in catalysis. BH4-responsive PAH deficiency is a variant of hyperphenylalaninemia or phenylketonuria (PKU) caused by mutations in the human PAH gene that respond to oral BH4 loading by stimulating enzyme activity and therefore lowering serum phenylalanine. Here, we showed in a coupled transcription-translation in vitro assay that upon expression in the presence of BH4, wild-type PAH enzyme activity was enhanced. We then investigated the effect of BH4 on PAH activity in transgenic mice that had a complete or partial deficiency in the endogenous cofactor biosynthesis. The rate of hepatic PAH enzyme activity increased significantly with BH4 content without affecting gene expression or Pah-mRNA stability. These results indicate that BH4 has a chaperon-like effect on PAH synthesis and/or is a protecting cofactor against enzyme auto-inactivation and degradation also in vivo. Our findings thus contribute to the understanding of the regulation of PAH by its cofactor BH4 on an additional level and provide a molecular explanation for cofactor-responsive PKU.
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| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
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| pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/5,6,7,8-tetrahydrobiopterin,
http://linkedlifedata.com/resource/pubmed/chemical/Biopterin,
http://linkedlifedata.com/resource/pubmed/chemical/Phenylalanine,
http://linkedlifedata.com/resource/pubmed/chemical/Phenylalanine Hydroxylase,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger
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| pubmed:status |
MEDLINE
|
| pubmed:month |
Nov
|
| pubmed:issn |
0014-5793
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| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:day |
19
|
| pubmed:volume |
577
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
507-11
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| pubmed:dateRevised |
2006-11-15
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| pubmed:meshHeading |
pubmed-meshheading:15556637-Amino Acid Metabolism, Inborn Errors,
pubmed-meshheading:15556637-Animals,
pubmed-meshheading:15556637-Animals, Newborn,
pubmed-meshheading:15556637-Biopterin,
pubmed-meshheading:15556637-Blotting, Western,
pubmed-meshheading:15556637-Gene Deletion,
pubmed-meshheading:15556637-Gene Expression Regulation, Enzymologic,
pubmed-meshheading:15556637-Genes, Recessive,
pubmed-meshheading:15556637-Heterozygote,
pubmed-meshheading:15556637-Humans,
pubmed-meshheading:15556637-Kinetics,
pubmed-meshheading:15556637-Liver,
pubmed-meshheading:15556637-Mice,
pubmed-meshheading:15556637-Mice, Knockout,
pubmed-meshheading:15556637-Mice, Transgenic,
pubmed-meshheading:15556637-Phenylalanine,
pubmed-meshheading:15556637-Phenylalanine Hydroxylase,
pubmed-meshheading:15556637-Phenylketonurias,
pubmed-meshheading:15556637-Protein Biosynthesis,
pubmed-meshheading:15556637-RNA, Messenger,
pubmed-meshheading:15556637-Transcription, Genetic
|
| pubmed:year |
2004
|
| pubmed:articleTitle |
Tetrahydrobiopterin protects phenylalanine hydroxylase activity in vivo: implications for tetrahydrobiopterin-responsive hyperphenylalaninemia.
|
| pubmed:affiliation |
Division of Clinical Chemistry and Biochemistry, Department of Pediatrics, University of Zürich, Steinwiesstrasse 75, CH-8032 Zürich, Switzerland. beat.thony@kispi.unizh.ch
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| pubmed:publicationType |
Journal Article,
Comparative Study,
Research Support, Non-U.S. Gov't
|