Obese gene expression: reduction by fasting and stimulation by insulin and glucose in lean mice, and persistent elevation in acquired (diet-induced) and genetic (yellow agouti) obesity

Mutations in the obese (ob) gene lead to obesity. This gene has been recently cloned, but the factors regulating its expression have not been elucidated. To address the regulation of the ob gene with regard to body weight and nutritional factors, Northern blot analysis was used to assess ob mRNA in...

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Veröffentlicht in:Proceedings of the National Academy of Sciences - PNAS 1996-04, Vol.93 (8), p.3434-3438
Hauptverfasser: Mizuno, T.M, Bergen, H, Funabashi, T, Kleopoulos, S.P, Zhong, Y.G, Bauman, W.A, Mobbs, C.V
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container_issue 8
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container_title Proceedings of the National Academy of Sciences - PNAS
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creator Mizuno, T.M
Bergen, H
Funabashi, T
Kleopoulos, S.P
Zhong, Y.G
Bauman, W.A
Mobbs, C.V
description Mutations in the obese (ob) gene lead to obesity. This gene has been recently cloned, but the factors regulating its expression have not been elucidated. To address the regulation of the ob gene with regard to body weight and nutritional factors, Northern blot analysis was used to assess ob mRNA in adipose tissue from mice [lean, obese due to diet, or genetically (yellow agouti) obese] under different nutritional conditions. ob mRNA was elevated in both forms of obesity, compared to lean controls, correlated with elevations in plasma insulin and body weight, but not plasma glucose. In lean C57BL/6J mice, but not in mice with diet-induced obesity, ob mRNA decreased after a 48-hr fast. Similarly, in lean C57BL/6J controls, but not in obese yellow mice, i.p. glucose injection significantly increased ob mRNA. For up to 30 min after glucose injection, ob mRNA in lean mice significantly correlated with plasma glucose, but not with plasma insulin. In a separate study with only lean mice, ob mRNA was inhibited >90% by fasting, and elevated approximately 2-fold 30 min after i.p. injection of either glucose or insulin. These results suggest that in lean animals glucose and insulin enhance ob gene expression. In contrast to our results in lean mice, in obese animals ob mRNA is elevated and relatively insensitive to nutritional state, possibly due to chronic exposure to elevated plasma insulin and/or glucose.
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This gene has been recently cloned, but the factors regulating its expression have not been elucidated. To address the regulation of the ob gene with regard to body weight and nutritional factors, Northern blot analysis was used to assess ob mRNA in adipose tissue from mice [lean, obese due to diet, or genetically (yellow agouti) obese] under different nutritional conditions. ob mRNA was elevated in both forms of obesity, compared to lean controls, correlated with elevations in plasma insulin and body weight, but not plasma glucose. In lean C57BL/6J mice, but not in mice with diet-induced obesity, ob mRNA decreased after a 48-hr fast. Similarly, in lean C57BL/6J controls, but not in obese yellow mice, i.p. glucose injection significantly increased ob mRNA. For up to 30 min after glucose injection, ob mRNA in lean mice significantly correlated with plasma glucose, but not with plasma insulin. In a separate study with only lean mice, ob mRNA was inhibited &gt;90% by fasting, and elevated approximately 2-fold 30 min after i.p. injection of either glucose or insulin. These results suggest that in lean animals glucose and insulin enhance ob gene expression. In contrast to our results in lean mice, in obese animals ob mRNA is elevated and relatively insensitive to nutritional state, possibly due to chronic exposure to elevated plasma insulin and/or glucose.</description><identifier>ISSN: 0027-8424</identifier><identifier>EISSN: 1091-6490</identifier><identifier>DOI: 10.1073/pnas.93.8.3434</identifier><identifier>PMID: 8622953</identifier><language>eng</language><publisher>United States: National Academy of Sciences of the United States of America</publisher><subject>adipose tissue ; Adipose tissues ; agouti gene ; animal models ; Animals ; Base Sequence ; blood glucose ; Body weight ; Diet ; DNA Primers - genetics ; Fasting ; Gene expression ; Gene Expression - drug effects ; Genes ; genetic obesity ; genetic regulation ; glucose ; Glucose - pharmacology ; High energy diets ; hormonal regulation ; hormones ; Insulin ; Insulin - pharmacology ; intraperitoneal injection ; leptin ; Male ; Messenger RNA ; Mice ; Mice, Inbred C57BL ; Mice, Inbred CBA ; Mice, Obese ; Molecular Sequence Data ; mutants ; Mutation ; nutrition ; nutritional status ; ob gene ; Obesity ; Obesity - etiology ; Obesity - genetics ; overfeeding ; polypeptides ; RNA ; RNA, Messenger - genetics ; RNA, Messenger - metabolism ; Rodents ; structural genes ; yellow agouti mice</subject><ispartof>Proceedings of the National Academy of Sciences - PNAS, 1996-04, Vol.93 (8), p.3434-3438</ispartof><rights>Copyright 1996 National Academy of Sciences</rights><rights>Copyright National Academy of Sciences Apr 16, 1996</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c603t-905f0f133085149c38ca849a695ac047da80f30c3bce31bccd3dad6404823c123</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://www.pnas.org/content/93/8.cover.gif</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/38978$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/38978$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,314,723,776,780,799,881,27901,27902,53766,53768,57992,58225</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8622953$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mizuno, T.M</creatorcontrib><creatorcontrib>Bergen, H</creatorcontrib><creatorcontrib>Funabashi, T</creatorcontrib><creatorcontrib>Kleopoulos, S.P</creatorcontrib><creatorcontrib>Zhong, Y.G</creatorcontrib><creatorcontrib>Bauman, W.A</creatorcontrib><creatorcontrib>Mobbs, C.V</creatorcontrib><title>Obese gene expression: reduction by fasting and stimulation by insulin and glucose in lean mice, and persistent elevation in acquired (diet-induced) and genetic (yellow agouti) obesity</title><title>Proceedings of the National Academy of Sciences - PNAS</title><addtitle>Proc Natl Acad Sci U S A</addtitle><description>Mutations in the obese (ob) gene lead to obesity. This gene has been recently cloned, but the factors regulating its expression have not been elucidated. To address the regulation of the ob gene with regard to body weight and nutritional factors, Northern blot analysis was used to assess ob mRNA in adipose tissue from mice [lean, obese due to diet, or genetically (yellow agouti) obese] under different nutritional conditions. ob mRNA was elevated in both forms of obesity, compared to lean controls, correlated with elevations in plasma insulin and body weight, but not plasma glucose. In lean C57BL/6J mice, but not in mice with diet-induced obesity, ob mRNA decreased after a 48-hr fast. Similarly, in lean C57BL/6J controls, but not in obese yellow mice, i.p. glucose injection significantly increased ob mRNA. For up to 30 min after glucose injection, ob mRNA in lean mice significantly correlated with plasma glucose, but not with plasma insulin. In a separate study with only lean mice, ob mRNA was inhibited &gt;90% by fasting, and elevated approximately 2-fold 30 min after i.p. injection of either glucose or insulin. These results suggest that in lean animals glucose and insulin enhance ob gene expression. 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This gene has been recently cloned, but the factors regulating its expression have not been elucidated. To address the regulation of the ob gene with regard to body weight and nutritional factors, Northern blot analysis was used to assess ob mRNA in adipose tissue from mice [lean, obese due to diet, or genetically (yellow agouti) obese] under different nutritional conditions. ob mRNA was elevated in both forms of obesity, compared to lean controls, correlated with elevations in plasma insulin and body weight, but not plasma glucose. In lean C57BL/6J mice, but not in mice with diet-induced obesity, ob mRNA decreased after a 48-hr fast. Similarly, in lean C57BL/6J controls, but not in obese yellow mice, i.p. glucose injection significantly increased ob mRNA. For up to 30 min after glucose injection, ob mRNA in lean mice significantly correlated with plasma glucose, but not with plasma insulin. In a separate study with only lean mice, ob mRNA was inhibited &gt;90% by fasting, and elevated approximately 2-fold 30 min after i.p. injection of either glucose or insulin. These results suggest that in lean animals glucose and insulin enhance ob gene expression. In contrast to our results in lean mice, in obese animals ob mRNA is elevated and relatively insensitive to nutritional state, possibly due to chronic exposure to elevated plasma insulin and/or glucose.</abstract><cop>United States</cop><pub>National Academy of Sciences of the United States of America</pub><pmid>8622953</pmid><doi>10.1073/pnas.93.8.3434</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record>
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source Jstor Complete Legacy; MEDLINE; PubMed Central; Alma/SFX Local Collection; Free Full-Text Journals in Chemistry
subjects adipose tissue
Adipose tissues
agouti gene
animal models
Animals
Base Sequence
blood glucose
Body weight
Diet
DNA Primers - genetics
Fasting
Gene expression
Gene Expression - drug effects
Genes
genetic obesity
genetic regulation
glucose
Glucose - pharmacology
High energy diets
hormonal regulation
hormones
Insulin
Insulin - pharmacology
intraperitoneal injection
leptin
Male
Messenger RNA
Mice
Mice, Inbred C57BL
Mice, Inbred CBA
Mice, Obese
Molecular Sequence Data
mutants
Mutation
nutrition
nutritional status
ob gene
Obesity
Obesity - etiology
Obesity - genetics
overfeeding
polypeptides
RNA
RNA, Messenger - genetics
RNA, Messenger - metabolism
Rodents
structural genes
yellow agouti mice
title Obese gene expression: reduction by fasting and stimulation by insulin and glucose in lean mice, and persistent elevation in acquired (diet-induced) and genetic (yellow agouti) obesity
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