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Characterization of cis-acting elements in the rat ATP citrate-lyase gene promoter
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  • Published: 01 March 2002

Characterization of cis-acting elements in the rat ATP citrate-lyase gene promoter

  • Young-An Moon1,
  • Sahng-Wook Park &
  • Kyung-Sup Kim 

Experimental & Molecular Medicine volume 34, pages 60–68 (2002)Cite this article

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Abstract

The cis-acting element in the promoter of the rat ATP-citrate lyase (ACL) and transcription factors which interact with these elements were determined. Six Sp1 binding sites and CAAT box exist in the region from transcription start site to -419 bp which showed the highest promoter activity in ACL promoter previously. In the region from -612 to -419, C/EBP binding site and other protein binding sites were also detected. Chloramphenicol acetyltransferase assay of ACL promoter suggested that multiple Sp1 sites might be involved in the ACL transcription. Gel mobility shift assay with antibodies against Sp1 and Sp3 revealed that DNA binding efficiency of Sp1 is increased in the liver of rats re-fed low fat/high carbohydrate diet after fasting. These results suggest that Sp1 is one of the most important transcription factors for ACL promoter to produce basal and induced transcription by low fat/high carbohydrate diet.

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Authors and Affiliations

  1. Department of Biochemistry & Molecular Biology, Institute of Genetic Science, Yonsei University College of Medicine, Seoul, Korea

    Young-An Moon

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  1. Young-An Moon
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  2. Sahng-Wook Park
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  3. Kyung-Sup Kim
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This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

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Moon, YA., Park, SW. & Kim, KS. Characterization of cis-acting elements in the rat ATP citrate-lyase gene promoter. Exp Mol Med 34, 60–68 (2002). https://doi.org/10.1038/emm.2002.9

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  • Published: 01 March 2002

  • Issue date: 01 March 2002

  • DOI: https://doi.org/10.1038/emm.2002.9

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Experimental & Molecular Medicine (Exp Mol Med)

ISSN 2092-6413 (online)

ISSN 1226-3613 (print)

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