The Human Fatty Acid Synthase Gene and De Novo Lipogenesis Are Coordinately Regulated in Human Adipose Tissue
Despite its potential importance in obesity and related disorders, little is known about regulation of lipogenesis in human adipose tissue. To investigate this area at the molecular and mechanistic levels, we studied lipogenesis and the regulation of 1 of its core enzymes, fatty acid synthase (FAS),...
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Published in | The Journal of nutrition Vol. 134; no. 5; pp. 1032 - 1038 |
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Main Authors | , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Bethesda, MD
Elsevier Inc
01.05.2004
American Society for Nutritional Sciences |
Subjects | |
Online Access | Get full text |
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Abstract | Despite its potential importance in obesity and related disorders, little is known about regulation of lipogenesis in human adipose tissue. To investigate this area at the molecular and mechanistic levels, we studied lipogenesis and the regulation of 1 of its core enzymes, fatty acid synthase (FAS), in human adipose tissue in response to hormonal and nutritional manipulation. As a paradigm for lipogenic genes, we cloned the upstream region of the human FAS gene, compared its sequence to that of FAS orthologs from other species, and identified important regulatory elements that lie upstream of the FAS coding region. Lipogenesis, as assessed by glucose incorporation into lipids, was increased by insulin and more so by the combination of insulin and dexamethasone (Dex, a potent glucocorticoid analogue). In parallel, FAS expression, activity, and gene transcription rate were also significantly increased by these treatments. We also showed that linoleic acid, a representative PUFA, attenuated the actions of insulin and Dex on fatty acid and lipid synthesis as well as FAS activity and expression. Using reporter assays, we determined that the regions responsible for hormonal regulation of the FAS gene lie in the proximal portion of the gene's 5′-flanking region, within which we identified an insulin response element similar to the E-box sequence we identified previously in the rat FAS gene. In summary, we demonstrated that lipogenesis occurs in human adipose tissue and can be induced by insulin, further enhanced by glucocorticoids, and suppressed by PUFA in a hormone-dependent manner. |
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AbstractList | Despite its potential importance in obesity and related disorders, little is known about regulation of lipogenesis in human adipose tissue. To investigate this area at the molecular and mechanistic levels, we studied lipogenesis and the regulation of 1 of its core enzymes, fatty acid synthase (FAS), in human adipose tissue in response to hormonal and nutritional manipulation. As a paradigm for lipogenic genes, we cloned the upstream region of the human FAS gene, compared its sequence to that of FAS orthologs from other species, and identified important regulatory elements that lie upstream of the FAS coding region. Lipogenesis, as assessed by glucose incorporation into lipids, was increased by insulin and more so by the combination of insulin and dexamethasone (Dex, a potent glucocorticoid analogue). In parallel, FAS expression, activity, and gene transcription rate were also significantly increased by these treatments. We also showed that linoleic acid, a representative PUFA, attenuated the actions of insulin and Dex on fatty acid and lipid synthesis as well as FAS activity and expression. Using reporter assays, we determined that the regions responsible for hormonal regulation of the FAS gene lie in the proximal portion of the gene's 5′-flanking region, within which we identified an insulin response element similar to the E-box sequence we identified previously in the rat FAS gene. In summary, we demonstrated that lipogenesis occurs in human adipose tissue and can be induced by insulin, further enhanced by glucocorticoids, and suppressed by PUFA in a hormone-dependent manner. |
Author | Standridge, Melissa Jones Voy, Brynn Wortman, Patrick Leuze, Michael Quigley, Neil Saxton, Arnold M. Andersen, Brett Joshi, Rashika Wang, Yanxin Moustaid-Moussa, Naima Soltani-Bejnood, Morvarid Chun, Joseph Urs, Sumithra Taylor, James W. Dhar, Madhu Claycombe, Kate Heo, Young-Ran Kim, Suyeon |
Author_xml | – sequence: 1 givenname: Yanxin surname: Wang fullname: Wang, Yanxin – sequence: 2 givenname: Sumithra surname: Urs fullname: Urs, Sumithra – sequence: 3 givenname: Suyeon surname: Kim fullname: Kim, Suyeon – sequence: 4 givenname: Morvarid surname: Soltani-Bejnood fullname: Soltani-Bejnood, Morvarid – sequence: 5 givenname: Neil surname: Quigley fullname: Quigley, Neil – sequence: 6 givenname: Young-Ran surname: Heo fullname: Heo, Young-Ran – sequence: 7 givenname: Melissa surname: Standridge fullname: Standridge, Melissa – sequence: 8 givenname: Brett surname: Andersen fullname: Andersen, Brett – sequence: 9 givenname: Rashika surname: Joshi fullname: Joshi, Rashika – sequence: 10 givenname: Patrick surname: Wortman fullname: Wortman, Patrick – sequence: 11 givenname: Naima surname: Moustaid-Moussa fullname: Moustaid-Moussa, Naima email: moustaid@utk.edu – sequence: 12 givenname: Brynn surname: Jones Voy fullname: Jones Voy, Brynn organization: Life Sciences Division, Oak Ridge National Laboratory, Oak Ridge, TN – sequence: 13 givenname: Madhu surname: Dhar fullname: Dhar, Madhu organization: Life Sciences Division, Oak Ridge National Laboratory, Oak Ridge, TN – sequence: 14 givenname: James W. surname: Taylor fullname: Taylor, James W. organization: Division of Plastic Surgery, Department of Surgery, University of Tennessee Medical Center, Knoxville, TN – sequence: 15 givenname: Joseph surname: Chun fullname: Chun, Joseph organization: Division of Plastic Surgery, Department of Surgery, University of Tennessee Medical Center, Knoxville, TN – sequence: 16 givenname: Michael surname: Leuze fullname: Leuze, Michael organization: Computer Science and Mathematics Division, Oak Ridge National Laboratory, Oak Ridge, TN – sequence: 17 givenname: Kate surname: Claycombe fullname: Claycombe, Kate organization: Department of Food Science and Nutrition, Michigan State University, E. Lansing, MI – sequence: 18 givenname: Arnold M. surname: Saxton fullname: Saxton, Arnold M. organization: Department of Animal Science, University of Tennessee, Knoxville, TN |
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Keywords | dexamethasone gene transcription DNL SREBP insulin KRBA linoleic acid PIA IRS Ins sequence BSA LA Dex FIRE FAS Human Acyltransferases Pancreatic hormone Dexamethasone Adipose tissue Enzyme Transferases Polyunsaturated fatty acid Lipids Insulin Fatty-acid synthase Linoleic acid Regulation(control) n-6 fatty acid Gene Unsaturated fatty acid Lipogenesis |
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Snippet | Despite its potential importance in obesity and related disorders, little is known about regulation of lipogenesis in human adipose tissue. To investigate this... |
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SubjectTerms | Adipose Tissue - enzymology Adipose Tissue - metabolism Adult Base Sequence Biological and medical sciences Culture Techniques dexamethasone Dexamethasone - pharmacology Fatty Acid Synthases - genetics Fatty Acids - biosynthesis Feeding. Feeding behavior Female Fundamental and applied biological sciences. Psychology Gene Expression Gene Expression Regulation gene transcription Glucocorticoids - pharmacology Glucose - metabolism Humans insulin Insulin - pharmacology linoleic acid Lipids - biosynthesis Middle Aged Molecular Sequence Data Promoter Regions, Genetic - physiology sequence Vertebrates: anatomy and physiology, studies on body, several organs or systems |
Title | The Human Fatty Acid Synthase Gene and De Novo Lipogenesis Are Coordinately Regulated in Human Adipose Tissue |
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