Advertisement
J. Lipid Res.
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowRequest Permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Moon, Y. S.
Right arrow Articles by Sul, H. S.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Moon, Y. S.
Right arrow Articles by Sul, H. S.
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati  
What's this?

Journal of Lipid Research, Vol. 43, 691-698, May 2002
Copyright © 2002 by Lipid Research, Inc.

Suppression of fatty acid synthase promoter by polyunsaturated fatty acids

Yang Soo Moon1, Maria-Jesus Latasa, Michael J. Griffin and Hei Sook Sul2

Department of Nutritional Sciences, University of California, Berkeley, CA 94720

2 To whom correspondence should be addressed. e-mail: hsul{at}nature.berkeley.edu

Dietary polyunsaturated fat is known to suppress expression of fatty acid synthase (FAS), a central enzyme in de novo lipogenesis. The sterol regulatory element-binding protein (SREBP) has recently been shown to be involved in this suppression. We previously reported that the first 2.1 kb of the FAS promoter are sufficient for transcriptional induction by a high carbohydrate diet as well as suppression by polyunsaturated fat in transgenic mice. Here, we first examined the DNA sequences responsible for SREBP-mediated suppression of FAS promoter activity by polyunsaturated fatty acids (PUFA) in vivo. Feeding polyunsaturated fat prevented both the low-level activation of the -278 FAS promoter which contains the -150 sterol response element (SRE), as well as the maximal activation of the longer -444 FAS promoter. We observed that ectopic expression of the activated form of SREBP in liver prevented PUFA-mediated suppression of both the endogenous FAS and FAS promoter-reporter transgene expression. We also found that the promoter region required for PUFA suppression in vivo is located between -278 to -131, where SREBP functions. Using HepG2 cells, we further examined the specific FAS promoter elements required for PUFA suppression. We found that the -150 SRE, as well as the –65 E-Box, contribute to PUFA suppression of the FAS promoter, at least in vitro.—Moon, Y. S., M-J. Latasa, M. J. Griffin, and H. S. Sul. Suppression of fatty acid synthase promoter by polyunsaturated fatty acids. J. Lipid Res. 2002. 43: 691–698.

Abbreviations: CAT, chloraphenicol acetyltransferase; FAS, fatty acid synthase; PEPCK, phosphoenolpyruvate carboxykinase; SREBP, sterol regulatory element binding protein; USF, upstream stimulatory factor

Supplementary key words SREBP • transgenic mice • -150 SRE • -65 E-box • HepG2


Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati    What's this?


This article has been cited by other articles:


Home page
Am. J. Physiol. Endocrinol. Metab.Home page
A. Radenne, M. Akpa, C. Martel, S. Sawadogo, D. Mauvoisin, and C. Mounier
Hepatic regulation of fatty acid synthase by insulin and T3: evidence for T3 genomic and nongenomic actions
Am J Physiol Endocrinol Metab, October 1, 2008; 295(4): E884 - E894.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
K. E. Matsukuma, L. Wang, M. K. Bennett, and T. F. Osborne
A Key Role for Orphan Nuclear Receptor Liver Receptor Homologue-1 in Activation of Fatty Acid Synthase Promoter by Liver X Receptor
J. Biol. Chem., July 13, 2007; 282(28): 20164 - 20171.
[Abstract] [Full Text] [PDF]


Home page
J. Nutr.Home page
E. S. Shin, H. H. Lee, S. Y. Cho, H. W. Park, S. J. Lee, and T. R. Lee
Genistein Downregulates SREBP-1 Regulated Gene Expression by Inhibiting Site-1 Protease Expression in HepG2 Cells
J. Nutr., May 1, 2007; 137(5): 1127 - 1131.
[Abstract] [Full Text] [PDF]


Home page
J. Nutr.Home page
Y. Wang, B. Jones Voy, S. Urs, S. Kim, M. Soltani-Bejnood, N. Quigley, Y.-R. Heo, M. Standridge, B. Andersen, M. Dhar, et al.
The Human Fatty Acid Synthase Gene and De Novo Lipogenesis Are Coordinately Regulated in Human Adipose Tissue
J. Nutr., May 1, 2004; 134(5): 1032 - 1038.
[Abstract] [Full Text] [PDF]


Home page
J. Lipid Res.Home page
A. Vecchini, V. Ceccarelli, F. Susta, P. Caligiana, P. Orvietani, L. Binaglia, G. Nocentini, C. Riccardi, G. Calviello, P. Palozza, et al.
Dietary {alpha}-linolenic acid reduces COX-2 expression and induces apoptosis of hepatoma cells
J. Lipid Res., February 1, 2004; 45(2): 308 - 316.
[Abstract] [Full Text] [PDF]


Home page
Mol. Cell. Biol.Home page
M.-J. Latasa, M. J. Griffin, Y. S. Moon, C. Kang, and H. S. Sul
Occupancy and Function of the -150 Sterol Regulatory Element and -65 E-Box in Nutritional Regulation of the Fatty Acid Synthase Gene in Living Animals
Mol. Cell. Biol., August 15, 2003; 23(16): 5896 - 5907.
[Abstract] [Full Text] [PDF]


Home page
J. Lipid Res.Home page
Y. Zhang, L. Yin, and F. B. Hillgartner
SREBP-1 integrates the actions of thyroid hormone, insulin, cAMP, and medium-chain fatty acids on ACC{alpha} transcription in hepatocytes
J. Lipid Res., February 1, 2003; 44(2): 356 - 368.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 All ASBMB Journals   Journal of Biological Chemistry 
 Molecular and Cellular Proteomics   ASBMB Today 
Copyright © 2002 by the American Society for Biochemistry and Molecular Biology.
Advertisement
spacer
Advertisement
Advertisement