Genomic organization and transcription units of the human acyl-CoA synthetase 3 gene.

Article Details

Citation

Minekura H, Kang MJ, Inagaki Y, Suzuki H, Sato H, Fujino T, Yamamoto TT

Genomic organization and transcription units of the human acyl-CoA synthetase 3 gene.

Gene. 2001 Oct 31;278(1-2):185-92.

PubMed ID
11707336 [ View in PubMed
]
Abstract

Acyl-CoA synthetases (ACSs) play an essential role in fatty acid metabolism. ACS3 is an arachidonate-preferring enzyme expressed in a wide range of human tissues including brain, heart, placenta, prostate, skeletal muscle, testis and thymus. As an initial step to understanding the transcriptional regulation of the human ACS3 gene, we analyzed the genomic organization and transcription units of the human ACS3 gene. Sequence analysis of genomic clones demonstrates that the human ACS3 gene spans at least 80.6 kb and contains 17 exons. The human ACS3 gene was mapped between the sequence-tagged site markers D2S360 and WI-21901. Sequence inspection of the 5'-flanking region revealed potential DNA elements including CCAAT, AP-1, Oct-1, GATAs, SRY, CdxA, Nkx-2.5, c-Myb, HSF2, NF-AT, AP-2, NF-Y, and p300. A minimal promoter region required for the expression of the human ACS3 gene in melanoma G361 cells was determined.

DrugBank Data that Cites this Article

Polypeptides
NameUniProt ID
Long-chain-fatty-acid--CoA ligase 3O95573Details