Gene expression of peroxisomal β-oxidation enzymes in rat brain

Molecular Brain Research

Volumn 74, Issue 1-2, 1999, Pages 217-220

  Knoll, Anja ^a   Sargueil, Françoise ^a   Salles, Jérôme ^a   Cassagne, Claude ^a,b   Garbay, Bertrand ^a  

^a University Victor Segalen   (France)

^b UNIVERSITÉ DE BORDEAUX   (France)

Author keywords

Brain; Development; Myelination; Peroxisomes; Very long chain fatty acids; Oxidation

Indexed keywords

3 HYDROXYACYL COENZYME A DEHYDROGENASE; ACETYL COENZYME A ACETYLTRANSFERASE; ACYL COENZYME A OXIDASE;

ANIMAL TISSUE; BRAIN; ENZYME ACTIVITY; FATTY ACID OXIDATION; GENE EXPRESSION; NONHUMAN; NORTHERN BLOTTING; PEROXISOME; POSTNATAL DEVELOPMENT; PRIORITY JOURNAL; RAT; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; SHORT SURVEY;

EID: 0033398191     PISSN: 0169328X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0169-328X(99)00252-1     Document Type: Article

References (19)

1. Antonenkov V.D., Van Veldhoven P.P., Waelkens E., Mannaerts G.P. Substrate specificities of 3-oxoacyl-CoA thiolase A and sterol carrier protein 2/3-oxoacyl-CoA thiolase purified from normal rat liver peroxisomes. J. Biol. Chem. 272:1997;26023-26031.
2. Bodnar A.G., Rachubinski R.A. Cloning and sequence determination of cDNA encoding a second rat liver peroxisomal 3-ketoacyl-CoA thiolase. Gene. 91:1990;193-199.
3. Chirgwin J.M., Przybyla A.E., Mc Donald R.J., Rutter W.J. Isolation of biologically active ribonucleic acid from sources enriched in ribonucleases. Biochemistry. 18:1979;5294-5299.
4. Dieuaide-Noubhani M., Asselberghs S., Mannaerts G.P., Van Veldhoven P.P. Evidence that multifunctional protein 2, and not multifunctional protein 1, is involved in the peroxisomal β-oxidation of pristanic acid. Biochem. J. 325:1997;367-373.
5. Miyazawa S., Hayashi H., Hijikata M., Ishii N., Furuta S., Kagamiyama H., Osumi T., Hashimoto T. Complete nucleotide sequence of cDNA and predicted amino acid sequence of rat acyl-CoA oxidase. J. Biol. Chem. 262:1987;8131-8137.
6. Ossendorp B.C., Wirtz K.W.A. The non-specific lipid-transfer protein (sterol carrier protein 2) and its relationship to peroxisomes. Biochimie. 75:1993;193-200.
7. Osumi T., Ishii N., Hijikata M., Kamijo K., Ozasa H., Furuta S., Miyazawa S., Kondo K., Inoue K., Kagamiyama H., Hashimoto T. Molecular cloning and nucleotide sequence of the cDNA for rat peroxisomal enoyl-CoA: hydratase-3-hydroxyacyl-CoA dehydrogenase bifunctional enzyme. J. Biol. Chem. 260:1985;8905-8910.
8. Osumi T., Ishii N., Miyazawa S., Hashimoto T. Isolation and structural characterization of the rat acyl-CoA oxidase gene. J. Biol. Chem. 262:1987;8138-8143.
9. Polous A. Very long chain fatty acids in higher animals - a review. Lipids. 30:1995;1-14.
10. Qin Y.M., Poutanen M.H., Helander H.M., Kvist A.P., Siivari K.M., Schmitz W., Conzelmann E., Hellman U., Hiltunen J.K. Peroxisomal multifunctional enzyme of β-oxidation metabolizing D-3-hydroxyacyl-CoA esters in rat liver: molecular cloning, expression and characterization. Biochim. J. 321:1997;21-28.
11. Reddy J.K., Mannaerts G.P. Peroxisomal lipid metabolism. Annu. Rev. Nutr. 14:1994;343-370.
12. Seedorf U., Assmann G. Cloning, expression, and nucleotide sequence of rat liver sterol carrier protein 2 cDNAs. J. Biol. Chem. 266:1991;630-636.
13. Seedorf U., Raabe M., Ellinghaus F., Kannenberg F., Fobker M., Engel T., Denis S., Wouters F., Wirtz K.W.A., Wanders R.J.A., Maeda N., Assmann G. Defective peroxisomal catabolism of branched fatty acyl-CoA in mice lacking the sterol carrier protein-2/sterol carrier protein-x gene function. Genes Dev. 12:1998;1189-1201.
14. Suzuki Y., Shimozawa N., Yajima S., Tomatsu S., Kondo N., Nakada Y., Akaboshi S., Lai M., Tanabe Y., Hashimoto T., Wanders R.J.A., Schutgens R.B.H., Moser H.W., Orii T. Novel subtype of peroxisomal acyl-CoA oxidase deficiency and bifunctional enzyme deficiency with detectable enzyme protein: identification by means of complementation analysis. Am. J. Hum. Genet. 54:1994;36-43.
15. Ushida T., Yamashita S. Molecular cloning, characterization, and expression in Escherichia coli of a cDNA encoding mammalian choline kinase. J. Biol. Chem. 269:1992;25795-25808.
16. Van Grunsven E.G., Van Berkel E., Mooijer P.A., Watkins P.A., Moser H.W., Suzuki Y., Jiang L.L., Hashimoto T., Hoefler G., Adamski J., Wanders R.J.A. Peroxisomal bifunctional protein deficiency revisited: resolution of its true enzymatic and molecular basis. Am. J. Hum. Genet. 64:1999;99-107.
17. Van Veldhoven P.P., Vanhove G., Asselberghs S., Eyssen H.J., Mannaerts G.P. Substrate specificities of rat liver peroxisomal acyl-CoA oxidase: Palmitoyl-CoA oxidase (inducible acyl-CoA oxidase), Pristanoyl-CoA oxidase (non-inducible acyl-CoA oxidase), and Trihydroxycoprostanoyl-CoA oxidase. J. Biol. Chem. 267:1992;20065-20074.
18. Vanhooren J.C.T., Fransen M., de Béthune B., Baumgart E., Baes M., Torrekens S., Van Leuven F., Mannaerts G.P., Van Veldhoven P.P. Rat pristanoyl-CoA oxidase cDNA cloning and recognition of its C-terminal (SQL) by the peroxisomal-targeting signal 1 receptor. Eur. J. Biochem. 239:1996;302-309.
19. Wanders R.J.A., Heymans H.S.A., Schutgens R.B.H., Barth P.G., Van den Bosch H., Tager J.M. Peroxisomal disorders in neurology. J. Neurosci. Res. 88:1988;1-39.