Literature DB >> 9271077

Evidence for the existence of a pristanoyl-CoA oxidase gene in man.

J C Vanhooren1, P Marynen, G P Mannaerts, P P Van Veldhoven.   

Abstract

In the rat, 2-methyl branched fatty acids and the bile acid intermediates di- and tri-hydroxycoprostanic acids are desaturated by pristanoyl-CoA oxidase and trihydroxycoprostanoyl-CoA oxidase respectively. In the human, these compounds are oxidized by a single enzyme, branched-chain acyl-CoA oxidase, which according to its amino acid sequence is the human homologue of rat trihydroxycoprostanoyl-CoA oxidase. Pristanoyl-CoA oxidase is apparently absent from human tissues as indicated by immunoblot analysis [Van Veldhoven, Van Rompuy, Fransen, de Béthune and Mannaerts (1994) Eur. J. Biochem. 222, 795-801] and Northern-blot analysis [Vanhooren, Fransen, de Béthune, Baumgart, Baes, Torrekens, Van Leuven, Mannaerts and Van Veldhoven (1996) Eur. J. Biochem. 239, 302-309] of human tissues. In this paper we present evidence, however, that at least the gene for pristanoyl-CoA oxidase is present in the human. A human liver cDNA encoding a protein of 700 amino acids, showing 75% amino acid identity with rat pristanoyl-CoA oxidase and harbouring a peroxisomal C-terminal-targeting signal (SKL), was isolated. Bacterial expression of the cDNA resulted in a fusion protein that was cross-reactive with antibodies directed against rat pristanoyl-CoA oxidase and the C-terminal SKL sequence. Screening of a genomic library with the isolated cDNA as a probe resulted in a genomic clone in which four introns were localized. By means of fluorescence in situ hybridization the gene for human pristanoyl-CoA oxidase was mapped at chromosome position 4p15.3. We conclude that a gene for pristanoyl-CoA oxidase is present in the human genome. The gene appears to be expressed to such a low extent in liver that its mRNA cannot be detected by routine Northern-blot analysis and that its product remains undetected by standard immunoblotting or by enzyme activity measurements. We speculate that the gene may be expressed under special (e.g. certain developmental stages) conditions or in certain specialized tissues not examined thus far.

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Year:  1997        PMID: 9271077      PMCID: PMC1218600          DOI: 10.1042/bj3250593

Source DB:  PubMed          Journal:  Biochem J        ISSN: 0264-6021            Impact factor:   3.857


  25 in total

1.  Separate peroxisomal oxidases for fatty acyl-CoAs and trihydroxycoprostanoyl-CoA in human liver.

Authors:  M Casteels; L Schepers; P P Van Veldhoven; H J Eyssen; G P Mannaerts
Journal:  J Lipid Res       Date:  1990-10       Impact factor: 5.922

2.  Large-scale purification and further characterization of rat pristanoyl-CoA oxidase.

Authors:  P P Van Veldhoven; P Van Rompuy; M Fransen; B De Béthune; G P Mannaerts
Journal:  Eur J Biochem       Date:  1994-06-15

3.  Rat pristanoyl-CoA oxidase. cDNA cloning and recognition of its C-terminal (SQL) by the peroxisomal-targeting signal 1 receptor.

Authors:  J C Vanhooren; M Fransen; B de Béthune; E Baumgart; M Baes; S Torrekens; F Van Leuven; G P Mannaerts; P P Van Veldhoven
Journal:  Eur J Biochem       Date:  1996-07-15

4.  Identification and purification of a peroxisomal branched chain fatty acyl-CoA oxidase.

Authors:  P P Van Veldhoven; G Vanhove; F Vanhoutte; G Dacremont; G Parmentier; H J Eyssen; G P Mannaerts
Journal:  J Biol Chem       Date:  1991-12-25       Impact factor: 5.157

5.  Purification and further characterization of peroxisomal trihydroxycoprostanoyl-CoA oxidase from rat liver.

Authors:  P P Van Veldhoven; P Van Rompuy; J C Vanhooren; G P Mannaerts
Journal:  Biochem J       Date:  1994-11-15       Impact factor: 3.857

6.  Isolation of the human peroxisomal acyl-CoA oxidase gene: organization, promoter analysis, and chromosomal localization.

Authors:  U Varanasi; R Chu; S Chu; R Espinosa; M M LeBeau; J K Reddy
Journal:  Proc Natl Acad Sci U S A       Date:  1994-04-12       Impact factor: 11.205

7.  Large deletion of the peroxisomal acyl-CoA oxidase gene in pseudoneonatal adrenoleukodystrophy.

Authors:  B Fournier; J M Saudubray; B Benichou; S Lyonnet; A Munnich; H Clevers; B T Poll-The
Journal:  J Clin Invest       Date:  1994-08       Impact factor: 14.808

8.  The CoA esters of 2-methyl-branched chain fatty acids and of the bile acid intermediates di- and trihydroxycoprostanic acids are oxidized by one single peroxisomal branched chain acyl-CoA oxidase in human liver and kidney.

Authors:  G F Vanhove; P P Van Veldhoven; M Fransen; S Denis; H J Eyssen; R J Wanders; G P Mannaerts
Journal:  J Biol Chem       Date:  1993-05-15       Impact factor: 5.157

9.  Molecular cloning and functional expression of a human peroxisomal acyl-coenzyme A oxidase.

Authors:  T Aoyama; K Tsushima; M Souri; T Kamijo; Y Suzuki; N Shimozawa; T Orii; T Hashimoto
Journal:  Biochem Biophys Res Commun       Date:  1994-02-15       Impact factor: 3.575

10.  Assignment of the human glypican gene (GPC1) to 2q35-q37 by fluorescence in situ hybridization.

Authors:  J R Vermeesch; G Mertens; G David; P Marynen
Journal:  Genomics       Date:  1995-01-01       Impact factor: 5.736

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  3 in total

Review 1.  Peroxisomal beta-oxidation enzymes.

Authors:  T Hashimoto
Journal:  Neurochem Res       Date:  1999-04       Impact factor: 3.996

2.  Acyl-coenzyme A oxidases 1 and 3 in brown trout (Salmo trutta f. fario): Can peroxisomal fatty acid β-oxidation be regulated by estrogen signaling?

Authors:  Tânia Vieira Madureira; L Filipe C Castro; Eduardo Rocha
Journal:  Fish Physiol Biochem       Date:  2015-10-27       Impact factor: 2.794

3.  Genome sequencing identifies a homozygous inversion disrupting QDPR as a cause for dihydropteridine reductase deficiency.

Authors:  Hardo Lilleväli; Sander Pajusalu; Monica H Wojcik; Julia Goodrich; Ryan L Collins; Ülle Murumets; Pille Tammur; Nenad Blau; Kersti Lilleväli; Katrin Õunap
Journal:  Mol Genet Genomic Med       Date:  2020-02-05       Impact factor: 2.183

  3 in total

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