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 inThe Journal of nutrition Vol. 134; no. 5; pp. 1032 - 1038
Main Authors Wang, Yanxin, Urs, Sumithra, Kim, Suyeon, Soltani-Bejnood, Morvarid, Quigley, Neil, Heo, Young-Ran, Standridge, Melissa, Andersen, Brett, Joshi, Rashika, Wortman, Patrick, Moustaid-Moussa, Naima, Jones Voy, Brynn, Dhar, Madhu, Taylor, James W., Chun, Joseph, Leuze, Michael, Claycombe, Kate, Saxton, Arnold M.
Format Journal Article
LanguageEnglish
Published Bethesda, MD Elsevier Inc 01.05.2004
American Society for Nutritional Sciences
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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.
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
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  givenname: Sumithra
  surname: Urs
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  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
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  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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Issue 5
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
Language English
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PublicationTitle The Journal of nutrition
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American Society for Nutritional Sciences
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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
URI https://dx.doi.org/10.1093/jn/134.5.1032
https://www.ncbi.nlm.nih.gov/pubmed/15113941
https://search.proquest.com/docview/71873334
Volume 134
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