Genomic DNA Sequence, Promoter Expression, and Chromosomal Mapping of Rat Muscle Carnitine Palmitoyltransferase I

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• 作者：Wang ; Dachun ; Harrison ; Wilbur ; Buja ; L. Maximilian ; Elder ; Frederick F. B. ; McMillin ; Jeanie B.
• 刊名：Genomics
• 出版年：1998
• 出版时间：March 15, 1998
• 年：1998
• 卷：48
• 期：3
• 页码：314-323
• 全文大小：633 K

文摘

Carnitine palmitoyltransferase I (CPT-I) is a key enzyme involved in the regulation of fatty acid oxidation. CPT-IA and CPT-IB are isoforms of carnitine palmitoyltransferase I, of which CPT-IA is expressed in liver, kidney, fibroblasts, and heart and CPT-IB is expressed in skeletal muscle, heart, brown and white adipocytes, and testes. Although the genomic DNA sequence of human CPT-IB is available, the transcription start site and upstream regulatory sequences are not known. For rat CPT-IB, only the cDNA sequence has been published. We have cloned the entire rat CPT-IB gene from a Lambda Fix II rat kidney genomic library. The genomic structure contains 19 exons, with the transcription start site for CPT-IB located in a short first exon, which is a 13-bp extension to the previously published cDNA 5′ sequence. The coding sequence is identical with the rat muscle cDNA. The rat CPT-IB gene contains 18 introns and 19 exons, the latter 18 exons showing 85 % homology to the human CPT-IB cDNA. CPT-IB maps to rat chromosome 7 at band q34. A putative promoter region was identified to within 391 bp of the transcription start site. The muscle specificity of the 5′ flanking region was verified by comparison of luciferase expression to that of β-galactosidase in cardiac myocytes and in HepG2 cells.