TY - JOUR
T1 - Peroxisomes contain a specific phytanoyl-CoA/pristanoyl-CoA thioesterase acting as a novel auxiliary enzyme in α- and β-oxidation of methyl-branched fatty acids in mouse
AU - Westin, Maria A.K.
AU - Hunt, Mary C.
AU - Alexson, Stefan E.H.
PY - 2007/9/14
Y1 - 2007/9/14
N2 - Phytanic acid and pristanic acid are derived from phytol, which enter the body via the diet. Phytanic acid contains a methyl group in position three and, therefore, cannot undergo β-oxidation directly but instead must first undergo α-oxidation to pristanic acid, which then enters β-oxidation. Both these pathways occur in peroxisomes, and in this study we have identified a novel peroxisomal acyl-CoA thioesterase named ACOT6, which we show is specifically involved in phytanic acid and pristanic acid metabolism. Sequence analysis of ACOT6 revealed a putative peroxisomal targeting signal at the C-terminal end, and cellular localization experiments verified it as a peroxisomal enzyme. Subcellular fractionation experiments showed that peroxisomes contain by far the highest phytanoyl-CoA/pristanoyl-CoA thioesterase activity in the cell, which could be almost completely immunoprecipitated using an ACOT6 antibody. Acot6 mRNA was mainly expressed in white adipose tissue and was co-expressed in tissues with Acox3 (the pristanoyl-CoA oxidase). Furthermore, Acot6 was identified as a target gene of the peroxisome proliferator-activated receptor α (PPARα) and is up-regulated in mouse liver in a PPARα-dependent manner.
AB - Phytanic acid and pristanic acid are derived from phytol, which enter the body via the diet. Phytanic acid contains a methyl group in position three and, therefore, cannot undergo β-oxidation directly but instead must first undergo α-oxidation to pristanic acid, which then enters β-oxidation. Both these pathways occur in peroxisomes, and in this study we have identified a novel peroxisomal acyl-CoA thioesterase named ACOT6, which we show is specifically involved in phytanic acid and pristanic acid metabolism. Sequence analysis of ACOT6 revealed a putative peroxisomal targeting signal at the C-terminal end, and cellular localization experiments verified it as a peroxisomal enzyme. Subcellular fractionation experiments showed that peroxisomes contain by far the highest phytanoyl-CoA/pristanoyl-CoA thioesterase activity in the cell, which could be almost completely immunoprecipitated using an ACOT6 antibody. Acot6 mRNA was mainly expressed in white adipose tissue and was co-expressed in tissues with Acox3 (the pristanoyl-CoA oxidase). Furthermore, Acot6 was identified as a target gene of the peroxisome proliferator-activated receptor α (PPARα) and is up-regulated in mouse liver in a PPARα-dependent manner.
UR - http://www.scopus.com/inward/record.url?scp=34848817129&partnerID=8YFLogxK
U2 - 10.1074/jbc.M703718200
DO - 10.1074/jbc.M703718200
M3 - Article
C2 - 17613526
AN - SCOPUS:34848817129
SN - 0021-9258
VL - 282
SP - 26707
EP - 26716
JO - Journal of Biological Chemistry
JF - Journal of Biological Chemistry
IS - 37
ER -