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Papers In Press, published online ahead of print December 19, 2002
Pharmacology, University of Tennessee, Memphis, TN 38163
Corresponding Author: epark{at}utmem.edu
Carnitine palmitoyltransferase-I (CPT-I) catalyzes the rate-controlling step of fatty acid oxidation. CPT-I converts long-chain fatty acyl-CoAs to acyl-carnitines for translocation across the mitochondrial membrane. The mRNA levels and enzyme activity of the liver isoform, CPT-I
J. Biol. Chem, 10.1074/jbc.M211062200
Submitted on October 29, 2002
Revised on December 16, 2002
Accepted on December 19, 2002
A thyroid hormone response unit formed between the promoter and first intron of the carnitine palmitoyltransferase-Ia gene mediates the liver specific induction by thyroid hormone
, are greatly increased in the liver of hyperthyroid animals. Thyroid hormone (T3) stimulates CPT-I
transcription far more robustly in the liver than in non-hepatic tissues. We have shown that the thyroid hormone receptor (TR) binds to a thyroid hormone response element (TRE) located in the CPT-I
promoter. In addition, elements in the first intron participate in the T3 induction of CPT-I
gene expression, but the CPT-I
intron alone cannot confer a T3 response. We found that deletion of sequences in the first intron between +653 and +744 decreased the T3 induction of CPT-I
. Upstream stimulatory factor (USF) and CCAAT enhancer binding proteins (C/EBPs) bind to elements within this region, and these factors are required for the T3 response. The binding of TR and C/EBP to the CPT-I
gene in vivo was shown by the chromatin immunoprecipitation assay. We determined that TR can physically interact with USF-1, USF-2 and C/EBP
. Transgenic mice were created that carry CPT-I
-Luciferase transgenes with or without the first intron of the CPT-I
gene. In these mouse lines, the first intron is required for the T3 induction as well as high levels of hepatic expression. Our data indicate that the T3 stimulates CPT-I
gene expression in the liver through a T3 response unit consisting of the TRE in the promoter and additional factors, C/EBP and USF, bound in the first intron.
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