This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
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 arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Fajas, L.
Right arrow Articles by Auwerx, J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Fajas, L.
Right arrow Articles by Auwerx, J.

 Previous Article  |  Next Article 

Molecular and Cellular Biology, August 1999, p. 5495-5503, Vol. 19, No. 8
0270-7306/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.

Regulation of Peroxisome Proliferator-Activated Receptor gamma  Expression by Adipocyte Differentiation and Determination Factor 1/Sterol Regulatory Element Binding Protein 1: Implications for Adipocyte Differentiation and Metabolism

Lluis Fajas,1,dagger Kristina Schoonjans,1 Laurent Gelman,1 Jae B. Kim,2 Jamila Najib,1 Genevieve Martin,1 Jean-Charles Fruchart,1 Michael Briggs,3,Dagger Bruce M. Spiegelman,2 and Johan Auwerx1,*

LBRE, U 325 INSERM, Institut Pasteur, F-59019 Lille, France1; Dana-Farber Cancer Institute, Harvard Medical School, Boston, Massachusetts 021152; and Ligand Pharmaceuticals, San Diego, California 921213

Received 28 October 1998/Returned for modification 3 December 1998/Accepted 12 May 1999


    ABSTRACT
Top
Abstract
Introduction
Materials and Methods
Results
Discussion
References

Peroxisome proliferator-activated receptor gamma  (PPARgamma ) is a nuclear receptor implicated in adipocyte differentiation and insulin sensitivity. We investigated whether PPARgamma expression is dependent on the activity of adipocyte differentiation and determination factor 1/sterol regulatory element binding protein 1 (ADD-1/SREBP-1), another transcription factor associated with both adipocyte differentiation and cholesterol homeostasis. Ectopic expression of ADD-1/SREBP-1 in 3T3-L1 and HepG2 cells induced endogenous PPARgamma mRNA levels. The related transcription factor SREBP-2 likewise induced PPARgamma expression. In addition, cholesterol depletion, a condition known to result in proteolytic activation of transcription factors of the SREBP family, induced PPARgamma expression and improved PPRE-driven transcription. The effect of the SREBPs on PPARgamma expression was mediated through the PPARgamma 1 and -3 promoters. Both promoters contain a consensus E-box motif that mediates the regulation of the PPARgamma gene by ADD-1/SREBP-1 and SREBP-2. These results suggest that PPARgamma expression can be controlled by the SREBP family of transcription factors and demonstrate new interactions between transcription factors that can regulate different pathways of lipid metabolism.


    INTRODUCTION
Top
Abstract
Introduction
Materials and Methods
Results
Discussion
References

Several transcription factors orchestrate the adipocyte differentiation process (reviewed in references 9, 13, and 43). These include the nuclear receptor peroxisome proliferator-activated receptor gamma  (PPARgamma ) (46, 47), the family of CCAAT enhancer binding proteins (C/EBP) (8, 15, 16, 53-55), and the basic helix-loop-helix leucine zipper transcription factor adipocyte differentiation and determination factor 1 (ADD-1) (21, 48), which was independently cloned as the sterol regulatory element binding protein 1 (SREBP-1), based on its role in cholesterol homeostasis (56). Current data suggest that C/EBPbeta and -delta induce the expression of PPARgamma (33, 54), which then triggers the adipogenic program. Terminal differentiation appears to require the concerted action of PPARgamma , C/EBPalpha , and ADD-1/SREBP-1 (21, 48). Several arguments support the important role of PPARgamma in adipocyte differentiation. First, ectopic expression of PPARgamma is sufficient to induce adipocyte conversion of fibroblasts (46, 47). In addition, PPARgamma together with C/EBPalpha can induce transdifferentiation of myoblasts into adipocytes (19). Second, the description of functional peroxisome proliferator-responsive elements (PPREs) in the regulatory sequences of several of the genes which are induced during adipocyte differentiation, such as the genes coding for adipocyte fatty acid binding protein aP2 (46), phosphoenolpyruvate carboxykinase (45), acyl coenzyme A (CoA) synthetase (36, 37), and lipoprotein lipase (35), is consistent with the crucial role attributed to PPARgamma in lipid metabolism. Finally, prostaglandin J2 derivatives, certain nonsteroidal anti-inflammatory drugs, and antidiabetic thiazolidinediones, which have been identified as natural and synthetic PPARgamma ligands, respectively (5, 14, 23-25, 51), all induce or enhance adipocyte differentiation (2, 3, 7, 14, 23, 24, 29, 47).

The identification of thiazolidinediones as PPARgamma ligands together with the central role which adipose tissue plays in the pathogenesis of important metabolic disorders, such as obesity and non-insulin-dependent diabetes mellitus, has generated a major drive to understand the regulation of PPARgamma gene expression. Since ADD-1/SREBP-1 and PPARgamma both are important during adipocyte differentiation, we analyzed PPARgamma expression in cells ectopically expressing ADD-1/SREBP-1. Increased levels of PPARgamma mRNA and protein were found under these conditions. SREBP-2 had similar effects on PPARgamma expression. It was furthermore shown that PPARgamma expression was influenced by cellular cholesterol levels in cells of both hepatic and adipocyte origin, an effect mediated by the SREBP family of transcription factors. The control of PPARgamma expression by the SREBP family of transcription factors is mediated through two sequence elements. First, there is a functional E-box in the PPARgamma 1 promoter. In addition, we also describe a functional E-box element located upstream of the exon A2 of the human PPARgamma gene, in the recently described PPARgamma 3 promoter (12). These observations suggest that regulatory interactions between the SREBPs and PPARgamma can coordinate cholesterol and fatty acid metabolism.


    MATERIALS AND METHODS
Top
Abstract
Introduction
Materials and Methods
Results
Discussion
References

Materials and oligonucleotides. The oligonucleotides used for various experiments in this report are listed in Table 1. BRL 49,653 and simvastatin were kind gifts of A. Nazdan of Ligand Pharmaceuticals and S. Wright from Merck Research Laboratories, respectively. All other chemicals, unless stated otherwise, were purchased from Sigma (St. Louis, Mo.).

                              
View this table:
[in this window]
[in a new window]
  		TABLE 1.   Oligonucleotides used in this study

Cell culture and retroviral infections. Standard cell culture conditions were used to maintain 3T3-L1 (obtained from American Type Culture Collection [ATCC]), HeLa (ATCC), RK-13 (ATCC), CCL-39 (a kind gift from Claude Sardet), and HepG2 cells (ATCC). BRL 49,653 and simvastatin were dissolved in dimethyl sulfoxide, and cholesterol and 25-hydroxycholesterol, linoleic acid, and linolenic acid were dissolved in ethanol. Prior to addition to cells, the fatty acids were complexed to bovine serum albumin (37). Control cells received vehicle only. Retroviral infection of 3T3-L1 cells was performed as described previously (21). Briefly, the BOSC23 cell line was transiently transfected with the recombinant retroviral vectors pBabe, ADD-1 403, and ADD-1 (21) by the calcium phosphate method. Viral supernatants were collected 48 h after transfection and titrated. 3T3-L1 cells were incubated with retrovirus for 5 h in the presence of 4 µg of Polybrene per ml. Cells were then subcultured (1:3) for 2 days after infection in medium containing puromycin (2 µg/ml) for selection. Differentiation of 3T3-L1 cells was performed as described previously (26).

RNA isolation and RNase protection assays. Total cellular RNA was prepared as described previously (32). Human and mouse PPARgamma (hPPARgamma and mPPARgamma , respectively) mRNA levels were determined by RNase protection assay with the templates previously described (12).

Western blot analysis of PPARgamma . Protein extraction, sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE), and electrotransfer were performed as described previously (11). The membranes were blocked overnight in blocking buffer (20 mM Tris, 100 mM NaCl, 1% Tween 20, 10% skim milk). Filters were first incubated for 4 h at 21°C with either a rabbit immunoglobulin G (IgG) anti-mPPARgamma (10 mg/ml) (11) or a rabbit IgG anti-mSREBP-1 antibody (Santa Cruz, Biotechnology, Calif.) and then for 1 h at 21°C with a goat anti-rabbit IgG (whole molecule) peroxidase conjugate diluted at 1/5,000. The complex was visualized with 4-chloro-1-naphthol as a reagent.

Analysis of promoter activity and transactivation assays. The PAC clone P-8856 (11), containing the full-length PPARgamma gene, was sequenced with the oligonucleotides LF-60 and LF-63 pointing upstream of exon A2. An 800-bp fragment of the PAC clone 8856 was isolated by PCR with the amplimers LF-60 (binding to the antisense strand in exon A2) and LF-68 (binding sense at position -800 of the PPARgamma 3 promoter). This PCR fragment was sequenced, inserted into the EcoRV site of pBluescript SK(+) (Stratagene, La Jolla, Calif.), and, after SpeI and KpnI restriction, subcloned into pGL3 (Promega, Madison, Wis.), creating the reporter vector pGL3gamma 3p800. For the construction of the reporter vector pGL3gamma 1p2000, the previously described pGL3gamma 1p3000 (11) was shortened by 1 kb at its 5' end by digestion with KpnI and PmlI. The reporter pGL3gamma 2p1000 was described previously (11). Site-directed mutagenesis of the E-box in the PPARgamma 3 promoter and the E-box in the PPARgamma 1 promoter was performed by splicing overlapping ends PCR (18), with the oligonucleotide pairs LF-106/LF-60 and LF-107/LF-68, to generate the plasmid pGL3gamma 3p800-E-boxmut, and the oligonucleotide pairs LF-145/LF-143 and LF-146/LF-144, to generate the plasmid pGL3gamma 1p2000-E-boxmut. This changed the three bases underlined in the sequence of the gamma 3 promoter 5'-ATTCATGTGACAT-3' to 5'-ATTCATGCATCAT-3' and the bases underlined in the sequence of the gamma 1 promoter 5'AGGATCACTTGAGCCC3' to 5'AGGATGCATTGAGCCC3'. The J3-TK-Luc (49) and ACO-TK-Luc (30) luciferase reporter vectors and the expression vectors encoding for ADD-1, a dominant-negative form of ADD-1, and SREBP-1a (48, 56) were described before. Transfections, luciferase, and beta -galactosidase assays were performed as described previously (37). To analyze the effect of cholesterol depletion in transfection experiments, the cells were divided into two pools after transfection. Half of the transfected cells were incubated with delipidated medium, whereas the other half of the cells were incubated with the same medium supplemented with a mixture of cholesterol (10 µM) and 25-hydroxycholesterol (1 µM).

Electrophoretic mobility shift assays (EMSAs) and oligonucleotide sequences. SREBP-1a protein was produced in a baculovirus system, and ADD-1 was produced by in vitro transcription. The quality of the proteins was verified by SDS-PAGE. Proteins were incubated for 15 min on ice in a total volume of 20 µl with 2.5 µg of poly(dI-dC), 1 µg of herring sperm DNA, and 1 ng of T4-polynucleotide kinase end-labelled double-stranded oligonucleotide corresponding either to the PPARgamma 1-E-box (LF-141) or the PPARgamma 3-E-box (LF-102) in binding buffer (10 mM Tris-HCl [pH 7.9], 40 mM KCl, 10% glycerol, 0.05% Nonidet P-40, 1 mM dithiothreitol). For competition experiments, increasing amounts of cold double-stranded oligonucleotides (10-, 50-, and 100-fold molar excess) corresponding to the PPARgamma 1-E-box, the PPARgamma 3-E-box, the consensus 3-hydroxy-3-methylglutaryl (HMG)-CoA synthase sterol response element (SRE) site (42), or the mutated PPARgamma 1-E-box (LF-143) and PPARgamma 3-E-box (LF-106) were included just before addition of labelled oligonucleotide. DNA-protein complexes were separated by electrophoresis on a 4% polyacrylamide gel in 0.25 × Tris-borate-EDTA buffer at 4°C (17).


    RESULTS
Top
Abstract
Introduction
Materials and Methods
Results
Discussion
References

Ectopic expression of ADD-1/SREBP-1 or SREBP-2 induces PPARgamma mRNA expression. In view of the adipogenic effects of ADD-1/SREBP-1, we investigated a potential role of ADD-1/SREBP-1 in the expression of the PPARgamma gene. For that purpose, HepG2 cells were electroporated with vectors expressing either SREBP-1a (56), ADD-1 (48), or SREBP-2 (20). RNA was extracted 48 h after transfection and analyzed by RNase protection assay for the presence of the PPARgamma 1 and PPARgamma 3 mRNAs. PPARgamma 1 mRNA levels were, as expected, the most abundant and were eight-, six-, and eightfold higher in the cells transfected with SREBP-1a, ADD-1, or SREBP-2, respectively (Fig. 1A, lanes 2 to 4). The same degree of induction was observed when the PPARgamma 3 mRNA levels were quantified. No induction of either PPARgamma 1 or -3 mRNAs was detected in cells transfected with an empty expression vector (Fig. 1A, lane 1). When a separate probe, designed to specifically detect PPARgamma 2 mRNA, was used in RNase protection assays, no changes in its mRNA levels were detected after transfection with either ADD-1/SREBP-1 or SREBP-2 (data not shown).


View larger version (49K):
[in this window]
[in a new window]
  		FIG. 1.   Increased expression of ADD-1, SREBP-1, or SREBP-2 induces PPARgamma mRNA expression. (A) RNase protection assay of total RNA from HepG2 cells transfected with either an empty vector (control [cont]; lane 1), an SREBP-1a expression vector (lane 2), an ADD-1 expression vector (lane 3), or an SREBP-2 expression vector (lane 4) or from human white adipose tissue (hWAT [as a positive control]; lane 5). Protected fragments corresponding to PPARgamma 1 and 3 mRNAs are indicated. Results were normalized with a 36B4 probe. Densitometric quantification of the results is shown. (B) RNase protection assay of total RNA from 3T3-L1 preadipocytes (lanes 3 to 5) or differentiated 3T3-L1 adipocytes (lanes 6 to 8) infected with an empty retroviral vector (lanes 3 and 6) or a retrovirus encoding ADD1-403 (lanes 4 and 7) or the full-length form of ADD-1 (lanes 5 and 8) as indicated. Lanes 1 and 2 show the undigested probes used to analyze PPARgamma and actin mRNA. An actin probe was used for normalization in this RNase protection assay. The fold induction of PPARgamma mRNA as determined by densitometric quantification of the results is shown in parentheses underneath the number of the lane.

To study the effects of ADD-1 on PPARgamma expression in more detail and in the context of adipocyte differentiation, 3T3-L1 cells were infected with either an empty retroviral vector, pBabe, or the same vector encoding full-length ADD-1 or the superactive ADD-1 403. Northern blot analysis showed that retroviral infection, by the virus encoding ADD-1, resulted in a twofold higher level of ADD-1 expression (data not shown). Infected cells were then cultured to confluence and consecutively treated with differentiation medium. Total RNA was isolated at confluence (preadipocytes) and at day 6 after confluence (adipocytes). The RNase protection assay indicated that the expression of PPARgamma mRNA was induced in both 3T3-L1 preadipocytes (threefold) and adipocytes (sevenfold) which ectopically express ADD-1 relative to cells which express the empty pBabe vector (Fig. 1B). Interestingly, a truncated form, ADD-1 403, equivalent to the proteolytically activated protein, which lacks the membrane-anchoring domain, was twofold more active in inducing PPARgamma expression in undifferentiated preadipocytes (Fig. 1B). These results suggest that the adipogenic effects of ADD-1/SREBP-1 previously demonstrated are at least in part due to an up-regulation of the PPARgamma gene expression.

PPARgamma protein expression is induced in cells grown under conditions which stimulate the activation of the SREBPs. In order to evaluate the possibility that PPARgamma was induced under more physiological conditions, associated with activation of the activation of SREBPs, we quantitated the relative expression of PPARgamma protein by Western blot analysis in undifferentiated 3T3-L1 cells (Fig. 2A) and HepG2 cells (Fig. 2B) grown in medium containing different cholesterol concentrations (50). In both cell lines, PPARgamma protein was induced at least ninefold upon cholesterol depletion during 24 h, a condition known to enhance the production of mature and active ADD-1/SREBP-1 (31, 50) (Fig. 2C). Interestingly, PPARgamma protein levels were decreased acutely by readdition of cholesterol (10 µM) and 25-hydroxycholesterol (1 µM) to the culture medium for 6 h (Fig. 2A and B, lane 3).


View larger version (29K):
[in this window]
[in a new window]
  		FIG. 2.   Cholesterol depletion induces PPARgamma expression. (A) Western blot analysis of nuclear extracts of 3T3-L1 preadipocytes with an anti-PPARgamma antibody. Preconfluent cells (lane 1) were incubated for 24 h (lane 2) in cholesterol-depleted medium. After 24 h of incubation in cholesterol-depleted medium, a mixture containing 10 µM cholesterol and 1 µM 25-OH-cholesterol was added to the medium for 6 additional h (24 + 6 chol) (lane 3). The fold induction of PPARgamma or SREBP as determined by densitometric quantification of the results is shown in parentheses underneath the number of the lane. (B) Similar Western blot experiments as described for panel A, but with HepG2 nuclear extracts instead of 3T3-L1 nuclear extracts. (C) Expression of SREBP-1 protein as detected after Western blot analysis of the 3T3-L1 nuclear extracts used in panel A. Western blotting was performed with an anti-SREBP-1 antiserum. (D) Western blot analysis of nuclear extracts of CCL-39 cells transfected with the constitutively active form of ADD-1, ADD-1 403. Cells were exposed to the same cholesterol depletion as specified for panel A.

In order to elucidate if the observed effects of cholesterol depletion on PPARgamma expression were mediated by ADD-1/SREBP-1, the same experiment was performed with the hamster lung cell line CCL-39 transfected with the constitutively active form of ADD-1, ADD-1 403. As expected, PPARgamma expression was induced sixfold in the cells transfected with ADD-1 403 (Fig. 2D, lane 2). No further changes in the expression of PPARgamma could be observed when cells were exposed to cholesterol-depleted medium (Fig. 2D, lane 3). As expected, in view of the cotransfection of ADD-1 403, no further reduction in PPARgamma levels was observed upon readdition of cholesterol to the medium. PPARgamma expression hence seems subject to a tight and fast control by alterations in intracellular cholesterol levels, and this effect is mediated by the SREBP family of transcription factors.

PPARgamma protein expression is induced in cells treated with HMG-CoA reductase inhibitors and is not affected by fatty acids. Treatment with HMG-CoA reductase inhibitors, which block the enzyme responsible for the rate-limiting step of cholesterol synthesis, provide another way to modify cellular cholesterol levels. Upon treatment with compounds such as compactin (mevastatin) or simvastatin, cells will become cholesterol depleted and the production of the active forms of ADD-1/SREBP-1 will increase (31, 40). Therefore, the expression of PPARgamma protein was evaluated in HepG2 cells before and after treatment with the potent HMG-CoA reductase inhibitor simvastatin. Treatment of the cells with simvastatin (5 × 10-7 M) for 6 h resulted in a robust and fast induction of PPARgamma protein levels (eightfold), which was sustained 12 h after addition (Fig. 3A), further supporting the notion that cellular cholesterol levels influence the expression of PPARgamma .


View larger version (37K):
[in this window]
[in a new window]
  		FIG. 3.   Inhibition of de novo cholesterol synthesis by statins induces PPARgamma expression. (A) Analysis of the PPARgamma protein by Western blotting of cell extracts from HepG2 cells incubated with medium supplemented with simvastatin (0.5 µM) for either 6 or 12 h. Fold induction of PPARgamma protein levels is shown in parentheses. (B) Quantification of PPARgamma protein levels in nuclear extracts from 3T3-L1 preadipocytes. Cells were lipid starved as in Fig. 2, and a mixture of linoleic acid (150 µM) and linolenic acid (150 µM) was added to the medium for a period of 12 h. An anti-PPARgamma specific antibody was used for Western blot analysis. Fold induction of PPARgamma protein levels is shown in parentheses.

Since polyunsaturated fatty acids have been reported to decrease the expression of promoters under the control of SREBP (44, 52), we analyzed whether the induction of PPARgamma protein expression upon cholesterol depletion was affected by the presence of fatty acids in the culture medium. As expected, when 3T3-L1 cells were incubated under lipid-free conditions, a significant induction of the levels of PPARgamma protein was observed (Fig. 3B, lane 2). Surprisingly, and in contrast to previous reports in the literature (44, 52), PPARgamma protein levels were not down-regulated when a mixture of linoleic and linolenic acids (150 µM each) was added to the lipid-depleted medium (Fig. 3B, lane 3).

Regulatory effect of ADD-1/SREBP-1 and SREBP-2 on the hPPARgamma 1 and -3 promoters. To investigate the possibility of a direct transcriptional effect of the SREBPs on PPARgamma expression, we analyzed the 5' upstream regulatory sequences of the human PPARgamma gene which we have previously determined (11). Therefore, we transfected CCL-39 cells with the pGL3gamma 1p2000, pGL3gamma 2p1000, and pGL3gamma 3p800 reporter plasmids (11), which contain, respectively 2 kb, 1 kb, and 800 bp of the human PPARgamma 1, -2, and -3 promoters. The activity of the pGL3gamma 1p2000 and pGL3gamma 3p800 reporter constructs was induced at least threefold when the ADD-1/SREBP-1 expression vector was cotransfected, suggesting that the increase in PPARgamma mRNA levels mentioned above was mediated by an effect on the proximal PPARgamma 1 and -3 promoters (Fig. 4A). Interestingly, whereas the activity of the pGL3gamma 1p2000 plasmid was significantly induced by ADD-1/SREBP-1, no such induction was observed with pGL3gamma 1p3000, which contains an additional 1,000 bp at it's 5' end, which suggests the presence of an inhibitory element in this region (data not shown). The activities of the PPARgamma 1 and -3 promoters were induced to a similar extent (at least threefold) when an expression vector for SREBP-2 was cotransfected instead of ADD-1/SREBP-1 or when cells were exposed to cholesterol-depleted medium (Fig. 4A). Consistent with our mRNA data, no effect of either cotransfection of ADD-1/SREBP-1 or SREBP-2 or cholesterol depletion could be observed on PPARgamma 2 promoter activity.


View larger version (28K):
[in this window]
[in a new window]
  		FIG. 4.   ADD-1/SREBP-1 and SREBP-2 transactivate the PPARgamma 1 and -3 promoters. (A) ADD-1/SREBP-1 and SREBP-2 transactivate the PPARgamma 1 and -3 promoters, but not the PPARgamma 2 promoter. Relative luciferase activity as determined after transfection of CCL-39 cells with the reporter constructs pGL3gamma 1p2000, pGL3gamma 2p1000, and pGL3gamma 3p800. Cells were either cotransfected with an empty expression vector (control) and exposed to medium containing cholesterol (10 µM) and 25-hydroxycholesterol (1 µM), cotransfected with an empty expression vector and maintained in cholesterol-depleted medium (Chol depletion), or cotransfected with an expression plasmid for SREBP-1 (SREBP-1) or SREBP-2 (SREBP-2) in medium containing cholesterol (10 µm) and 25-hydroxycholesterol (1 µM). Results are expressed as fold induction and represent the mean ± standard deviation of three independent experiments. Statistically significant differences by Student's t test (P < 0.05) are indicated. (B) A scheme of the genomic structure of the 5' end of the human PPARgamma gene and of the approximate location of the response elements. Exons 1 to 6 are shared by all three subtypes. PPARgamma 1 contains in addition the untranslated exons A1 and A2; PPARgamma 2 contains exon B, which is translated; and PPARgamma 3 contains only the untranslated exon A2. The respective hPPARgamma promoters are indicated by arrows. The approximate locations of the E-boxes are indicated.

ADD-1/SREBP-1 controls the hPPARgamma expression through E-box motifs in the gamma 1 and gamma 3 promoters. In order to investigate whether the induction of PPARgamma 1 and -3 expression was the consequence of direct binding of the SREBPs to the PPARgamma 1 and -3 promoters, a detailed computer-assisted sequence homology analysis was performed. Potential binding sites for the SREBP transcription factor family, corresponding to putative E-box motifs, were detected in both the PPARgamma 1 and PPARgamma 3 promoters (see Fig. 4B for the scheme). In order to demonstrate direct binding of ADD-1/SREBP-1 to the putative PPARgamma 1-E-box (at position -1535 from the transcription initiation site 5' of the exon A1) and the PPARgamma 3-E-box (at position -341 from the transcription initiation site 5' of the A2 exon), we used double-stranded oligonucleotides corresponding to the PPARgamma 1-E-box (LF-141) and PPARgamma 3-E-box (LF-102) as probes in EMSAs. Baculovirus-produced and partially purified SREBP-1a, a different splice variant of the ADD-1/SREBP-1 gene, is capable of binding to both sites. Competition gel shift assays using increasing amounts of cold double-stranded oligonucleotides containing either the sites mentioned above (PPARgamma 1-E-box [Fig. 5A] or PPARgamma 3-E-box [Fig. 5C]), the consensus SRE of the HMG-CoA synthase gene (42), or the mutated PPARgamma 1-E-boxmut (from AGGATCACTTGAGCCC to AGGATGCATTGAGCCC) and PPARgamma 3-E-boxmut (from ATTCATGTGACAT to ATTCATGCATCAT), were performed next in order to demonstrate the specificity of the binding (Fig. 5A and C). Binding of SREBP-1a to the PPARgamma 1-E-box is competed by both the cold PPARgamma 1-E-box (Fig. 5A, lanes 2 to 3) and by the consensus SRE oligonucleotides (Fig. 5A, lanes 5 and 6), whereas the mutated PPARgamma 1-E-boxmut oligonucleotide was unable to compete with the PPARgamma 1-E-box for binding of SREBP-1a (Fig. 5A, lanes 8 and 9). Similarly, cold PPARgamma 3-E-box and the consensus SRE oligonucleotides were able to compete for the binding of SREBP-1a to the PPARgamma 3-E-box probe (Fig. 5C, lanes 2 to 4 and 5 to 7), whereas the mutated PPARgamma 3-E-boxmut was not (Fig. 5C, lanes 8 to 10). Similar EMSA results were obtained when SREBP-2 was used (data not shown).


View larger version (49K):
[in this window]
[in a new window]
  		FIG. 5.   Binding of ADD-1/SREBP-1 to the PPARgamma 1 and -3 promoters. (A) EMSA with a partially purified baculovirus-produced SREBP-1a protein, a different splice variant of ADD-1, and a labelled double-stranded oligonucleotide representing the PPARgamma 1-E-box. Competition experiments were performed with cold oligonucleotides representing either the PPARgamma 1-E-box (gamma 1-E-box; LF-141), the consensus HMG-CoA synthase SRE site (SREcons) (42), or the mutated PPARgamma 1-E-box (gamma 1-E-boxmut; LF-143) at either 10-, 50-, or 100-fold molar excess. (B) Sequence of the wild-type and mutated PPARgamma 1-E-box. The consensus E-box is indicated in bold characters. The three bases which are mutated are indicated underneath the original bases. (C) EMSA performed under exactly the same conditions as described for panel A with the PPARgamma 3-E-box (LF-102) as a labelled double-stranded oligonucleotide and the mutated PPARgamma 3-E-box (gamma 3 E-boxmut; LF-106) as a competitor instead of the PPARgamma 1-E-box and gamma 1-E-boxmut, respectively. (D) Sequence of the wild-type and mutated PPARgamma 3 E-boxes. The consensus E-box is underlined, whereas a potential SRE is indicated in boldface. The three bases mutated are indicated underneath the original bases.

To unequivocally demonstrate that it is through binding to the PPARgamma 1-E-box and PPARgamma 3-E-box that ADD-1/SREBP-1 and SREBP-2 stimulate the activity of the hPPARgamma 1 and -3 promoters, we substituted, respectively, three bases in the PPARgamma 1-E-box (Fig. 5B) and in the PPARgamma 3-E-box (Fig. 5D) in the context of the native PPARgamma 1 and -3 promoters to generate the pGL3gamma 1p2000-E-boxmut and pGL3gamma 3p800-E-boxmut reporter plasmids. In contrast to the wild-type reporter vectors (Fig. 6A), cotransfected ADD-1/SREBP-1 or SREBP-2 was unable to stimulate the activity of the mutated pGL3gamma 1p2000-E-boxmut and pGL3gamma 3p800-E-boxmut reporter vectors in the CCL-39 lung-derived cell line (Fig. 6B).


View larger version (32K):
[in this window]
[in a new window]
  		FIG. 6.   The PPARgamma 1-E-box and the PPARgamma 3-E-box mediate the induction of the PPARgamma gene by ADD-1/SREBP-1 and SREBP-2. Relative luciferase activity as determined after transfection of CCL39 cells with the reporter constructs pGL3gamma 1p2000, pGL3gamma 1p2000-E-boxmut, pGL3gamma 3p800, and pGL3gamma 3p800-E-boxmut. Cells were cotransfected with either an empty expression vector (control) or an expression plasmid for SREBP-1 or SREBP-2. Values are the mean ± standard deviation of three independent experiments. Statistically significant differences (P < 0.05) by Student's t test are indicated by asterisks.

PPARgamma activity is stimulated by activation of ADD-1/SREBP-1. Next we assessed whether the changes in endogenous PPARgamma expression mentioned above, induced by modulating the cholesterol concentration in the medium, were associated with altered expression of a PPRE-driven reporter gene. We transfected the J3-TK-Luc luciferase reporter gene, which contains three copies of the PPRE of the apolipoprotein A-II gene J site (49), into rabbit kidney-derived RK-13 cells and maintained half of the cells in cholesterol-depleted medium, whereas the other half were grown in the same medium supplemented with a mixture of cholesterol and 25-hydroxycholesterol. Under both conditions, increasing amounts of the synthetic PPARgamma ligand BRL 49,653 were added to the medium, resulting in a dose-dependent activation of promoter activity by BRL 49,653 (Fig. 7A). Under conditions of cholesterol depletion, the reporter gene was, however, activated to a significantly higher level. In fact, the BRL 49,653 dose-response curve was shifted proportionally, keeping the slope constant and suggesting that the observed effect of cholesterol depletion was the result of increased expression of the PPARgamma protein. Similar results were obtained when 3T3-L1 (Fig. 7B) and ob-1771 preadipocyte cells were used (data not shown). Consistent with the effect of synthetic PPARgamma agonists, addition of the fatty acid linolenic acid (C18:3 at 400 µM) to the medium resulted in a roughly similar fold of induction of the PPRE-driven reporter gene in cholesterol-depleted or cholesterol-containing medium (Fig. 7C). In order to exclude the possibility that the observed effect was specific for the apolipoprotein A-II PPRE, we performed a cotransfection experiment with a different luciferase reporter driven by a single copy of the PPRE from the acyl CoA oxidase (ACO) gene (ACO-TK-Luc [30]). Also, the activity of the ACO-TK-Luc reporter was significantly induced by cholesterol depletion (Fig. 7D).


View larger version (24K):
[in this window]
[in a new window]
  		FIG. 7.   Transactivation of PPARgamma is enhanced under conditions of cholesterol depletion. (A and B) Promoter activity of the PPRE-driven luciferase reporter vector J3-TK-Luc after addition of different doses of BRL 49,653 in cells maintained in medium with (dashed squares) or without added cholesterol (10 µM) and 25-hydroxycholesterol (1 µM) (open squares). The results in RK-13 cells (A) and in 3T3-L1 preadipocytes (B) are shown. The results represent the mean ± standard deviation of three independent experiments. Differences between the two conditions were statistically significant. RLU, relative light units. (C) Activity of the J3-TK-Luc reporter gene is stimulated by linolenic acid (C18:3 [400 µM]) in RK-13 cells. Cells were transfected with J3-TK-Luc reporter constructs and maintained for an additional 16 h in medium with (open bars; upper part of the graph) or without added cholesterol (10 µM) and 25-hydroxycholesterol (1 µM) (hatched bars; lower part of the panel). Cells grown under these basal conditions (control cells [C]) were compared with cells treated with BRL 49653 (1 µM [BRL]) or linolenic acid (400 µM [FA]). The results represent the mean ± standard deviation of three independent experiments. The asterisks are indicative of significant differences between the stimulated cells and controls by Student's t test (P < 0.05). (D) Activity of both the J3-TK-Luc and ACO-TK-Luc reporter genes is stimulated by cholesterol depletion in undifferentiated 3T3-L1 cells. Cells were transfected with J3-TK-Luc or ACO-TK-Luc reporter constructs and incubated under the same conditions than in panel C. The results represent the mean ± standard deviation of three independent experiments. The asterisks are indicative of significant differences by Student's t test (P < 0.05).


    DISCUSSION
Top
Abstract
Introduction
Materials and Methods
Results
Discussion
References

PPARgamma has been identified as one of the key factors controlling adipocyte differentiation (6, 13). Full differentiation of preadipocytes into adipocytes is regulated by a complex interplay of the C/EBP family, the PPARgamma proteins, and ADD-1/SREBP-1 (13). Although it has been reported that C/EBPalpha , ADD-1/SREBP-1, and PPARgamma by themselves can promote adipocyte differentiation, an orchestrated action of all these factors is most likely required to trigger adipocyte differentiation effectively. We demonstrated here that ADD-1/SREBP-1 and SREBP-2 directly control the expression of the human PPARgamma gene at a transcriptional level.

ADD-1/SREBP-1 and SREBP-2 have a dual specificity in DNA binding and have been shown to be capable of interacting both with E-box sequences and SREs (21). EMSAs and cotransfection assays demonstrated that the ADD-1/SREBP-1 family of transcription factors can stimulate the expression of the PPARgamma 1 promoter and the expression of the recently cloned PPARgamma 3 promoter through binding to E-box motives which are present in both promoters. Previously it has been shown that ectopically expressed ADD-1/SREBP-1 can increase the number of fibroblasts undergoing adipocyte differentiation (reference 21 and unpublished data). Our data suggest that one of the mechanisms by which ADD-1/SREBP-1 might exert its adipogenic action is through the induction of PPARgamma expression, which in its turn will induce the expression of downstream adipocyte target genes (Fig. 7). This hence suggests that the ADD-1/SREBP-1 family might function as proximal regulatory factors relative to PPARgamma in the induction of adipocyte differentiation. Furthermore, the induction of PPARgamma expression and consequent stimulation of lipogenesis could contribute to the massive cholesterol and fatty acid accumulation seen in the livers of animals overexpressing the mature form of SREBP-1a (38) and the more moderate fatty acid accumulation observed in animals overexpressing SREBP-1c (39). Interestingly, the observation that transgenic mice overexpressing SREBP-1c, under the control of the adipose tissue-specific aP2 promoter, are lipodystrophic (41) appears at odds with the general proadipogenic effect of ADD-1/SREBP-1 (21, 38, 39) and suggests that SREBP-1c under certain conditions could negatively influence adipogenesis. The differences between this last study (41) and previous work (21, 38, 39), as well as our present data, are most likely explained by differential effects SREBP-1c might have at different steps during the development of adipose tissue (11a).

In addition to the transcriptional induction of PPARgamma , ADD-1/SREBP-1 induces the expression of several important genes involved in lipogenesis in the adipocyte, such as fatty acid synthase (4, 21, 38), acetyl CoA carboxylase (27, 38), glycerol-3-phosphate acyltransferase (10), and the lipoprotein lipase gene (21, 33a, 38). These ADD-1/SREBP-1 target genes control important steps in fatty acid metabolism, which may lead to the production of natural fatty acid-derived PPAR ligands and activators, suggesting a second more indirect pathway by which ADD-1/SREBP-1 regulates adipocyte differentiation (i.e., by controlling the production of natural activators of PPARgamma ) (22) (Fig. 8). Besides this important regulatory effect of cholesterol and the ADD-1/SREBP-1 family of transcription factors on fatty acid metabolism, fatty acids were recently also reported to inhibit the maturation of ADD-1/SREBP-1 and decrease the expression of promoters driven by sterol regulatory elements (44, 52). Interestingly, we did not observe an effect of unsaturated fatty acids on the induction of PPARgamma expression by cholesterol depletion (Fig. 3B). Furthermore, fatty acids were like thiazolidinediones capable of further inducing expression of a PPRE-driven reporter gene to a similar level in medium with or without sterols (Fig. 7C). All of this suggests that in the case of PPARgamma , the inhibitory effects of fatty acids might be insufficient to overcome the potent stimulatory effects of cholesterol depletion on PPARgamma expression or, alternatively, that the addition of fatty acids might have an independent and direct stimulatory effect on PPARgamma expression. In addition, the absence of PPARgamma expression in medium with cholesterol (Fig. 2A and B, lanes 1 and 3) would obscure any further inhibitory effect fatty acids might have on this regulation.


View larger version (6K):
[in this window]
[in a new window]
  		FIG. 8.   Scheme summarizing the different links between ADD-1/SREBP activation and PPARgamma activity. The present report provides evidence that PPARgamma expression is induced by ADD-1/SREBP, whereas the role of ADD-1/SREBP in inducing PPARgamma ligands was described before (22).

Interestingly, the implications of the control of PPARgamma expression by the ADD-1/SREBP-1 family of transcription factors and cholesterol may extend beyond the control of adipogenesis and affect total body lipid and glucose metabolism. First, in view of the important insulin sensitization which accompanies PPARgamma activation in vivo, the regulation of PPARgamma expression and activity by changes in cellular cholesterol concentration suggests that cholesterol homeostasis could have an impact on whole-body glucose homeostasis. Further in vivo studies exploring this issue are definitely needed. Second, the regulation of the expression of PPARgamma , a nuclear receptor that is activated by fatty acid metabolites, by the cholesterol-regulated transcription factors of the ADD-1/SREBP-1 family, links transcriptional control by these two important classes of lipids. Changes in intracellular cholesterol levels will, via modulation of ADD-1/SREBP-1 and/or SREBP-2 activity (31, 40, 50), profoundly affect fatty acid and triglyceride metabolism, which is controlled by PPARgamma activity. One interesting example of such an interrelationship between cholesterol and fatty acid metabolism, is the observation that powerful HMG-CoA reductase inhibitors, such as simvastatin (28) or atorvastatin (1), not only reduce circulating cholesterol but also reduce triglyceride levels. Whereas the reduction in cholesterol levels could be explained by their inhibitory effect on the key enzyme controlling cholesterol biosynthesis, HMG-CoA reductase, no explanation is available for their beneficial effect on triglyceride levels. Cholesterol depletion induced by these agents, however, leads to proteolytic activation of the ADD-1/SREBP family (31, 40). If this causes an induction in PPARgamma levels, as shown here, the increased PPARgamma transcriptional activity would be expected to induce the expression of several genes involved in triglyceride clearance (for review, see reference 34). Hence, this mode of interaction between transcription factors controlling different lipid pathways may provide an explanation for both the somewhat unexpected triglyceride-lowering effects that have been observed when these cholesterol-lowering agents have been used in this therapeutic context and for the pronounced beneficial effects of the statins in patients with diabetic hyperlipidemia. This new knowledge could provide a basis for development of agents which have a broader or more specific ability to regulate different aspects of lipid metabolism.


    ACKNOWLEDGMENTS

The technical help of D. Cayet and C. Haby and the support of and/or discussion with A. Negro-Villar, R. Heyman, M. Leibowitz, D. Moller, S. Wright, and D. De Chaffoy are kindly acknowledged. We acknowledge the gift of materials from Samuel Wright and Alex Nadzan.

This work was supported by grants from INSERM, Région Nord-Pas-de-Calais, Institut Pasteur, Université de Lille II, ARC (no. 6403), and Ligand pharmaceuticals. J.A. is a research director with the CNRS, and K.S. is a research assistant with INSERM. L.F. was supported by the Janssen Research Foundation.


    FOOTNOTES

* Corresponding author. Mailing address: LBRE, U 325 INSERM, Département d'Athérosclérose, Institut Pasteur, 1 Rue Calmette, F-59019 Lille, France. Phone: (33)-320-87 77 88. Fax: (33)-320-87 73 60. E-mail: Johan.Auwerx{at}pasteur-lille.fr.

dagger Present address: Institut de Génétique Moleculaire de Montpellier, F-34000 Montpellier, France.

Dagger Present address: Cardiovascular Pharmacology, SmithKline Beecham Pharmaceuticals, King of Prussia, PA 19406.


    REFERENCES
Top
Abstract
Introduction
Materials and Methods
Results
Discussion
References

1. Alaupovic, P., T. Heinonen, L. Shurzinske, and D. M. Black. 1997. Effect of a new HMG-CoA reductase inhibitor, atorvastatin, on lipids, apolipoproteins and lipoprotein particles in patients with elevated serum cholesterol and triglyceride levels. Atherosclerosis 133:123-133[Medline].
2. Amri, E.-Z., B. Bertrand, G. Ailhaud, and P. Grimaldi. 1991. Regulation of adipose cell differentiation. I. Fatty acids are inducers of the aP2 gene expression. J. Lipid Res. 32:1449-1456[Abstract].
3. Aubert, J., G. Ailhaud, and R. Negrel. 1996. Evidence for a novel regulatory pathway activated by (carba)prostacyclin in preadipose and adipose cells. FEBS Lett. 397:117-121[Medline].
4. Bennet, M. K., J. M. Lopez, H. B. Sanchez, and T. F. Osborne. 1995. Sterol regulation of fatty acid synthase promoter:coordinate feedback regulation of two major lipid pathways. J. Biol. Chem. 270:25578-25583[Abstract/Free Full Text].
5. Berger, J., P. Bailey, C. Biswas, C. A. Cullinan, T. W. Doebber, N. S. Hayes, R. Saperstein, R. G. Smith, and M. D. Leibowitz. 1996. Thiazolidinediones produce a conformational change in peroxisomal proliferator-activated receptor-gamma : binding and activation correlate with antidiabetic actions in db/db mice. Endocrinology 137:4189-4195[Abstract].
6. Brun, R. P., J. B. Kim, E. Hu, and B. M. Spiegelman. 1997. Peroxisome proliferator-activated receptor gamma and the control of adipogenesis. Curr. Opin. Lipidol. 8:212-218[Medline].
7. Chawla, A., and M. A. Lazar. 1994. Peroxisome proliferator and retinoid signaling pathways co-regulate preadipocyte phenotype and survival. Proc. Natl. Acad. Sci. USA 91:1786-1790[Abstract/Free Full Text].
8. Christy, R. J., V. W. Yang, J. M. Ntambi, D. E. Geiman, W. H. Landschulz, A. D. Friedman, Y. Nakabeppu, T. J. Kelly, and M. D. Lane. 1989. Differentiation-induced gene expression in 3T3-L1 preadipocytes: CCAAT/enhancer binding protein interacts with and activates the promoters of two adipocyte-specific genes. Genes Dev. 3:1323-1335[Abstract/Free Full Text].
9. Cornelius, P., O. A. MacDougald, and M. D. Lane. 1994. Regulation of adipocyte development. Annu. Rev. Nutr. 14:99-129[Medline].
10. Ericsson, J., S. M. Jackson, J. B. Kim, B. M. Spiegelman, and P. A. Edwards. 1997. Identification of glycerol-3-phosphate acyltransferase as an adipocyte determination and differentiation factor 1- and sterol regulatory element-binding protein-responsive gene. J. Biol. Chem. 272:7298-7305[Abstract/Free Full Text].
11. Fajas, L., D. Auboeuf, E. Raspe, K. Schoonjans, A. M. Lefebvre, R. Saladin, J. Najib, M. Laville, J. C. Fruchart, S. Deeb, A. Vidal-Puig, J. Flier, M. R. Briggs, B. Staels, H. Vidal, and J. Auwerx. 1997. Organization, promoter analysis and expression of the human PPARgamma gene. J. Biol. Chem. 272:18779-18789[Abstract/Free Full Text].
11a. Fajas, L., and J. Auwerx. Unpublished results.
12. Fajas, L., J. C. Fruchart, and J. Auwerx. 1998. PPARgamma 3 mRNA: a distinct PPARgamma mRNA subtype transcribed from an independent promoter. FEBS Lett. 438:55-60[Medline].
13. Fajas, L., J. C. Fruchart, and J. Auwerx. 1998. Transcriptional control of adipogenesis. Curr. Opin. Cell Biol. 10:165-173[Medline].
14. Forman, B. M., P. Tontonoz, J. Chen, R. P. Brun, B. M. Spiegelman, and R. M. Evans. 1995. 15-Deoxy-Delta 12,14 prostaglandin J2 is a ligand for the adipocyte determination factor PPARgamma . Cell 83:803-812[Medline].
15. Freytag, S. O., and T. J. Geddes. 1992. Reciprocal regulation of adipogenesis by Myc and C/EBPalpha . Science 256:379-382[Abstract/Free Full Text].
16. Freytag, S. O., D. L. Paielli, and J. D. Gilbert. 1994. Ectopic expression of the CCAAT/enhancer-binding protein alpha  promotes the adipogenic program in a variety of mouse fibroblastic cells. Genes Dev. 8:1654-1663[Abstract/Free Full Text].
17. Fried, M. G., and D. M. Crothers. 1983. CAP and RNA polymerase interactions with the lac promoter: binding stoichiometry and long range effects. Nucleic Acids Res. 11:141-158[Abstract/Free Full Text].
18. Ho, S. N., H. D. Hunt, N. M. Horton, J. K. Pullen, and L. R. Pease. 1989. Side directed mutagenesis by overlap extension using the polymerase chain reaction. Gene 77:51-59[Medline].
19. Hu, E., P. Tontonoz, and B. M. Spiegelman. 1995. Transdifferentiation of myoblasts by the adipogenic transcription factors PPARgamma and C/EBPalpha . Proc. Natl. Acad. Sci. USA 92:9856-9860[Abstract/Free Full Text].
20. Hua, X., C. Yokoyama, J. Wu, M. R. Briggs, M. S. Brown, J. L. Goldstein, and X. Wang. 1993. SREBP-2, a second basic-helix-loop-helix leucine zipper protein that stimulates transcription by binding to a sterol regulatory element. Proc. Natl. Acad. Sci. USA 90:11603-11607[Abstract/Free Full Text].
21. Kim, J. B., and B. M. Spiegelman. 1996. ADD1/SREBP1 promotes adipocyte differentiation and gene expression linked to fatty acid metabolism. Genes Dev. 10:1096-1107[Abstract/Free Full Text].
22. Kim, J. B., H. M. Wright, M. Wright, and B. M. Spiegelman. 1998. ADD1/SREBP1 activates PPARgamma through the production of endogenous ligand. Proc. Natl. Acad. Sci. USA 95:4333-4337[Abstract/Free Full Text].
23. Kliewer, S. A., J. M. Lenhard, T. M. Willson, I. Patel, D. C. Morris, and J. M. Lehman. 1995. A prostaglandin J2 metabolite binds peroxisome proliferator-activated receptor gamma  and promotes adipocyte differentiation. Cell 83:813-819[Medline].
24. Lehmann, J. M., J. M. Lenhard, B. B. Oliver, G. M. Ringold, and S. A. Kliewer. 1997. Peroxisome proliferator-activated receptors alpha  and gamma  are activated by indomethacin and other non-steroidal anti-inflammatory drugs. J. Biol. Chem. 272:3406-3410[Abstract/Free Full Text].
25. Lehmann, J. M., L. B. Moore, T. A. Smith-Oliver, W. O. Wilkison, T. M. Willson, and S. A. Kliewer. 1995. An antidiabetic thiazolidinedione is a high affinity ligand for peroxisome proliferator-activated receptor gamma  (PPARgamma ). J. Biol. Chem. 270:12953-12956[Abstract/Free Full Text].
26. Lin, F. T., and M. D. Lane. 1992. Antisense CCAAT/enhancer binding protein RNA suppresses coordinate gene expression and triglyceride accumulation during differentiation of 3T3-L1 adipocytes. Genes Dev. 6:533-544[Abstract/Free Full Text].
27. Lopez, J. M., M. K. Bennett, H. B. Sanchez, J. M. Rosenfeld, and T. F. Osborne. 1996. Sterol regulation of acetyl coenzyme A carboxylase: a mechanism for coordinate control of cellular lipid. Proc. Natl. Acad. Sci. USA 93:1049-1053[Abstract/Free Full Text].
28. Mol, M. J. T. M., D. W. Erkelens, J. A. Gevers Leuven, J. A. Schouten, and A. F. H. Stalenhoef. 1986. Effects of synvinolin (MK-733) on plasma lipids in familial hypercholesterolemia. In Lancet:936-939.
29. Negrel, R., D. Gaillard, and G. Ailhaud. 1989. Prostacyclin as a potent effector of adipose-cell differentiation. Biochem. J. 257:399-405[Medline].
30. Osumi, T., J. K. Wen, and T. Hashimoto. 1991. Two cis-acting regulatory elements in the peroxisome proliferator-responsive element enhancer region of rat acyl-CoA oxidase gene. Biochem. Biophys. Res. Commun. 175:866-871[Medline].
31. Sakai, J., E. A. Duncan, R. B. Rawson, X. Hua, M. S. Brown, and J. L. Goldstein. 1996. Sterol-regulated release of SREBP-2 from cell membranes requires two sequential cleavages, one within a transmembrane segment. Cell 85:1037-1046[Medline].
32. Saladin, R., P. De Vos, M. Guerre-Millo, A. Leturque, J. Girard, B. Staels, and J. Auwerx. 1995. Transient increase in obese gene expression after food intake and insulin administration. Nature 377:527-529[Medline].
33. Saladin, R., L. Fajas, S. Dana, Y. D. Halvorsen, J. Auwerx, and M. Briggs. 1999. Differential regulation of peroxisome proliferator activated receptor gamma 1 (PPARgamma 1) and PPARgamma 2 mRNA expression in early stages of adipogenesis. Cell Growth Differ. 10:43-48[Abstract/Free Full Text].
33a. Schoonjans, K. Unpublished data.
34. Schoonjans, K., G. Martin, B. Staels, and J. Auwerx. 1997. Peroxisome proliferator-activated receptors, orphans with ligands and functions. Curr. Opin. Lipidol. 8:159-166[Medline].
35. Schoonjans, K., J. Peinado-Onsurbe, A. M. Lefebvre, R. Heyman, M. Briggs, S. Deeb, B. Staels, and J. Auwerx. 1996. PPARalpha and PPARgamma activators direct a tissue-specific transcriptional response via a PPRE in the lipoprotein lipase gene. EMBO J. 15:5336-5348[Medline].
36. Schoonjans, K., B. Staels, P. Grimaldi, and J. Auwerx. 1993. Acyl-CoA synthetase mRNA expression is controlled by fibric-acid derivatives, feeding and liver proliferation. Eur. J. Biochem. 216:615-622[Medline].
37. Schoonjans, K., M. Watanabe, H. Suzuki, A. Mahfoudi, G. Krey, W. Wahli, P. Grimaldi, B. Staels, T. Yamamoto, and J. Auwerx. 1995. Induction of the acyl-coenzyme A synthetase gene by fibrates and fatty acids is mediated by a peroxisome proliferator response element in the C promoter. J. Biol. Chem. 270:19269-19276[Abstract/Free Full Text].
38. Shimano, H., J. D. Horton, R. E. Hammer, I. Shimomura, M. S. Brown, and J. L. Goldstein. 1996. Overproduction of cholesterol and fatty acids causes massive liver enlargement in transgenic mice expressing truncated SREBP-1a. J. Clin. Investig. 98:1575-1584[Medline].
39. Shimano, H., J. D. Horton, I. Shimomura, R. E. Hammer, M. S. Brown, and J. L. Goldstein. 1997. Isoform 1c of sterol regulatory element binding protein is less active than isoform 1a in livers of transgenic mice and in cultured cells. J. Clin. Investig. 99:846-854[Medline].
40. Shimomura, I., Y. Bashmakov, H. Shimano, J. D. Horton, J. L. Goldstein, and M. S. Brown. 1997. Cholesterol feeding reduces nuclear forms of sterol regulatory element binding proteins in hamster liver. Proc. Natl. Acad. Sci. USA 94:12345-12359.
41. Shimomura, I., R. E. Hammer, J. A. Richardson, S. Ikemoto, Y. Bashmakov, J. L. Goldstein, and M. S. Brown. 1998. Insulin resistance and diabetes mellitus in transgenic mice expressing nuclear SREBP-1c in adipose tissue: a model for congenital generalized lipodystrophy. Genes Dev. 12:3182-3194[Abstract/Free Full Text].
42. Smith, J. R., T. F. Osborne, M. S. Brown, J. L. Goldstein, and G. Gil. 1988. Multiple sterol regulatory elements in the promoter for hamster 3-hydroxy-3-methylglutaryl coenzyme A synthase. J. Biol. Chem. 263:18480-18487[Abstract/Free Full Text].
43. Spiegelman, B. M., and J. S. Flier. 1996. Adipogenesis and obesity: rounding out the big picture. Cell 87:377-389[Medline].
44. Thewke, D. P., S. R. Panini, and M. Sinensky. 1998. Oleate potentiates oxysterol inhibition of transcription from sterol regulatory element-1-regulated promoters and maturation of sterol regulatory element-binding proteins. J. Cell. Biochem. 273:21402-21407.
45. Tontonoz, P., E. Hu, J. Devine, E. G. Beale, and B. M. Spiegelman. 1995. PPARgamma 2 regulates adipose expression of the phosphoenolpyruvate carboxykinase gene. Mol. Cell. Biol. 15:351-357[Abstract].
46. Tontonoz, P., E. Hu, R. A. Graves, A. I. Budavari, and B. M. Spiegelman. 1994. mPPARgamma 2: tissue-specific regulator of an adipocyte enhancer. Genes Dev. 8:1224-1234[Abstract/Free Full Text].
47. Tontonoz, P., E. Hu, and B. M. Spiegelman. 1994. Stimulation of adipogenesis in fibroblasts by PPARgamma 2, a lipid-activated transcription factor. Cell 79:1147-1156[Medline].
48. Tontonoz, P., J. B. Kim, R. A. Graves, and B. M. Spiegelman. 1993. ADD1: a novel helix-loop-helix transcription factor associated with adipocyte determination and differentiation. Mol. Cell. Biol. 13:4753-4759[Abstract/Free Full Text].
49. Vu-Dac, N., K. Schoonjans, V. Kosykh, J. Dallongeville, J.-C. Fruchart, B. Staels, and J. Auwerx. 1995. Fibrates increase human apolipoprotein A-II expression through activation of the peroxisome proliferator-activated receptor. J. Clin. Investig. 96:741-750.
50. Wang, X., R. Sato, M. S. Brown, X. Hua, and J. L. Goldstein. 1994. SREBP-1, a membrane-bound transcription factor released by sterol-regulated proteolysis. Cell 77:53-62[Medline].
51. Willson, T. M., J. E. Cobb, D. J. Cowan, R. W. Wiethe, I. D. Correa, S. R. Prakash, K. D. Beck, L. B. Moore, S. A. Kliewer, and J. M. Lehmann. 1996. The structure activity relationship between peroxisome proliferator activated receptor gamma  agonism and the antihyperglycemic activity of thiazolidinediones. J. Med. Chem. 39:665-668[Medline].
52. Worgall, T. S., S. L. Sturley, T. Seo, T. F. Osborne, and R. J. Deckelbaum. 1998. Polyunsaturated fatty acids decrease expression of promoters with sterol regulatory elements by decreasing levels of mature sterol regulatory element-binding protein. J. Biol. Chem. 273:25537-25540[Abstract/Free Full Text].
53. Wu, Z., N. L. R. Bucher, and S. R. Farmer. 1996. Induction of peroxisome proliferator-activated receptor gamma  during the conversion of 3T3 fibroblasts into adipocytes is mediated by C/EBPbeta , C/EBPdelta , and glucocorticoids. Mol. Cell. Biol. 16:4128-4136[Abstract].
54. Wu, Z., Y. Xie, N. L. R. Bucher, and S. R. Farmer. 1995. Conditional ectopic expression of C/EBPbeta in NIH-3T3 cells induces PPARgamma and stimulates adipogenesis. Genes Dev. 9:2350-2363[Abstract/Free Full Text].
55. Yeh, W. C., Z. Cao, M. Classon, and S. McKnight. 1995. Cascade regulation of terminal adipocyte differentiation by three members of the C/EBP family of leucine zipper proteins. Genes Dev. 9:168-181[Abstract/Free Full Text].
56. Yokoyama, C., X. Wang, M. R. Briggs, A. Admon, J. Wu, X. Hua, J. L. Goldstein, and M. S. Brown. 1993. SREBP-1, a basic helix-loop-helix-leucine zipper protein that controls transcription of the LDL receptor gene. Cell 75:187-197[Medline].

Molecular and Cellular Biology, August 1999, p. 5495-5503, Vol. 19, No. 8
0270-7306/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.


This article has been cited by other articles:

  • Marfella, R., Di Filippo, C., Portoghese, M., Barbieri, M., Ferraraccio, F., Siniscalchi, M., Cacciapuoti, F., Rossi, F., D'Amico, M., Paolisso, G. (2009). Myocardial lipid accumulation in patients with pressure-overloaded heart and metabolic syndrome. J. Lipid Res. 50: 2314-2323 [Abstract] [Full Text]  
  • Marfella, R, Portoghese, M, Ferraraccio, F, Siniscalchi, M, Babieri, M, Di Filippo, C, D'Amico, M, Rossi, F, Paolisso, G (2009). Thiazolidinediones may contribute to the intramyocardial lipid accumulation in diabetic myocardium: effects on cardiac function. Heart 95: 1020-1022 [Full Text]  
  • Ohoka, N., Kato, S., Takahashi, Y., Hayashi, H., Sato, R. (2009). The Orphan Nuclear Receptor ROR{alpha} Restrains Adipocyte Differentiation through a Reduction of C/EBP{beta} Activity and Perilipin Gene Expression. Mol. Endocrinol. 23: 759-771 [Abstract] [Full Text]  
  • Tisdale, M. J. (2009). Mechanisms of Cancer Cachexia. Physiol. Rev. 89: 381-410 [Abstract] [Full Text]  
  • Pou, J., Rebollo, A., Roglans, N., Sanchez, R. M., Vazquez-Carrera, M., Laguna, J. C., Pedro-Botet, J., Alegret, M. (2008). Ritonavir Increases CD36, ABCA1 and CYP27 Expression in THP-1 Macrophages. Exp. Biol. Med. 233: 1572-1582 [Abstract] [Full Text]  
  • Desai, M., Guang Han, , Ferelli, M., Kallichanda, N., Lane, R. H. (2008). Programmed Upregulation of Adipogenic Transcription Factors in Intrauterine Growth-Restricted Offspring. Reproductive Sciences 15: 785-796 [Abstract]  
  • Madsen, L., Petersen, R. K., Steffensen, K. R., Pedersen, L. M., Hallenborg, P., Ma, T., Froyland, L., Doskeland, S. O., Gustafsson, J.-A., Kristiansen, K. (2008). Activation of Liver X Receptors Prevents Statin-induced Death of 3T3-L1 Preadipocytes. J. Biol. Chem. 283: 22723-22736 [Abstract] [Full Text]  
  • Takahashi, Y., Ohoka, N., Hayashi, H., Sato, R. (2008). TRB3 suppresses adipocyte differentiation by negatively regulating PPAR{gamma} transcriptional activity. J. Lipid Res. 49: 880-892 [Abstract] [Full Text]  
  • Desjardins, F., Sekkali, B., Verreth, W., Pelat, M., De Keyzer, D., Mertens, A., Smith, G., Herregods, M.-C., Holvoet, P., Balligand, J.-L. (2008). Rosuvastatin increases vascular endothelial PPAR{gamma} expression and corrects blood pressure variability in obese dyslipidaemic mice. Eur Heart J 29: 128-137 [Abstract] [Full Text]  
  • Paumelle, R., Staels, B. (2007). Peroxisome Proliferator-Activated Receptors Mediate Pleiotropic Actions of Statins. Circ. Res. 100: 1394-1395 [Full Text]  
  • Yano, M., Matsumura, T., Senokuchi, T., Ishii, N., Murata, Y., Taketa, K., Motoshima, H., Taguchi, T., Sonoda, K., Kukidome, D., Takuwa, Y., Kawada, T., Brownlee, M., Nishikawa, T., Araki, E. (2007). Statins Activate Peroxisome Proliferator-Activated Receptor {gamma} Through Extracellular Signal-Regulated Kinase 1/2 and p38 Mitogen-Activated Protein Kinase-Dependent Cyclooxygenase-2 Expression in Macrophages. Circ. Res. 100: 1442-1451 [Abstract] [Full Text]  
  • Sarov-Blat, L., Kiss, R. S., Haidar, B., Kavaslar, N., Jaye, M., Bertiaux, M., Steplewski, K., Hurle, M. R., Sprecher, D., McPherson, R., Marcel, Y. L. (2007). Predominance of a Proinflammatory Phenotype in Monocyte-Derived Macrophages From Subjects With Low Plasma HDL-Cholesterol. Arterioscler. Thromb. Vasc. Bio. 27: 1115-1122 [Abstract] [Full Text]  
  • Desruisseaux, M. S., Nagajyothi, , Trujillo, M. E., Tanowitz, H. B., Scherer, P. E. (2007). Adipocyte, Adipose Tissue, and Infectious Disease. Infect. Immun. 75: 1066-1078 [Full Text]  
  • Nichol, D., Christian, M., Steel, J. H., White, R., Parker, M. G. (2006). RIP140 Expression Is Stimulated by Estrogen-related Receptor {alpha} during Adipogenesis. J. Biol. Chem. 281: 32140-32147 [Abstract] [Full Text]  
  • Karagiannides, I., Thomou, T., Tchkonia, T., Pirtskhalava, T., Kypreos, K. E., Cartwright, A., Dalagiorgou, G., Lash, T. L., Farmer, S. R., Timchenko, N. A., Kirkland, J. L. (2006). Increased CUG Triplet Repeat-binding Protein-1 Predisposes to Impaired Adipogenesis with Aging. J. Biol. Chem. 281: 23025-23033 [Abstract] [Full Text]  
  • Desvergne, B., Michalik, L., Wahli, W. (2006). Transcriptional Regulation of Metabolism. Physiol. Rev. 86: 465-514 [Abstract] [Full Text]  
  • Munteanu, A., Taddei, M., Tamburini, I., Bergamini, E., Azzi, A., Zingg, J.-M. (2006). Antagonistic Effects of Oxidized Low Density Lipoprotein and {alpha}-Tocopherol on CD36 Scavenger Receptor Expression in Monocytes: INVOLVEMENT OF PROTEIN KINASE B AND PEROXISOME PROLIFERATOR-ACTIVATED RECEPTOR-{gamma}. J. Biol. Chem. 281: 6489-6497 [Abstract] [Full Text]  
  • Boguslavsky, R. L., Stewart, C. L., Worman, H. J. (2006). Nuclear lamin A inhibits adipocyte differentiation: implications for Dunnigan-type familial partial lipodystrophy. Hum Mol Genet 15: 653-663 [Abstract] [Full Text]  
  • Isley, W. L., Miles, J. M., Patterson, B. W., Harris, W. S. (2006). The effect of high-dose simvastatin on triglyceride-rich lipoprotein metabolism in patients with type 2 diabetes mellitus. J. Lipid Res. 47: 193-200 [Abstract] [Full Text]  
  • Brandebourg, T. D., Hu, C. Y. (2005). Isomer-specific regulation of differentiating pig preadipocytes by conjugated linoleic acids. J ANIM SCI 83: 2096-2105 [Abstract] [Full Text]  
  • Brandebourg, T. D., Hu, C. Y. (2005). Regulation of differentiating pig preadipocytes by retinoic acid. J ANIM SCI 83: 98-107 [Abstract] [Full Text]  
  • Ulven, S. M., Dalen, K. T., Gustafsson, J.-A., Nebb, H. I. (2004). Tissue-specific autoregulation of the LXR{alpha} gene facilitates induction of apoE in mouse adipose tissue. J. Lipid Res. 45: 2052-2062 [Abstract] [Full Text]  
  • Landrier, J.-F., Thomas, C., Grober, J., Duez, H., Percevault, F., Souidi, M., Linard, C., Staels, B., Besnard, P. (2004). Statin Induction of Liver Fatty Acid-Binding Protein (L-FABP) Gene Expression Is Peroxisome Proliferator-activated Receptor-{alpha}-dependent. J. Biol. Chem. 279: 45512-45518 [Abstract] [Full Text]  
  • Ando, H., Tsuruoka, S., Yamamoto, H., Takamura, T., Kaneko, S., Fujimura, A. (2004). Effects of Pravastatin on the Expression of ATP-Binding Cassette Transporter A1. J. Pharmacol. Exp. Ther. 311: 420-425 [Abstract] [Full Text]  
  • Hadri, K. E., Glorian, M., Monsempes, C., Dieudonne, M.-N., Pecquery, R., Giudicelli, Y., Andreani, M., Dugail, I., Feve, B. (2004). In Vitro Suppression of the Lipogenic Pathway by the Nonnucleoside Reverse Transcriptase Inhibitor Efavirenz in 3T3 and Human Preadipocytes or Adipocytes. J. Biol. Chem. 279: 15130-15141 [Abstract] [Full Text]  
  • Horton, J. D., Shimomura, I., Ikemoto, S., Bashmakov, Y., Hammer, R. E. (2003). Overexpression of Sterol Regulatory Element-binding Protein-1a in Mouse Adipose Tissue Produces Adipocyte Hypertrophy, Increased Fatty Acid Secretion, and Fatty Liver. J. Biol. Chem. 278: 36652-36660 [Abstract] [Full Text]  
  • Wang, C., Pattabiraman, N., Zhou, J. N., Fu, M., Sakamaki, T., Albanese, C., Li, Z., Wu, K., Hulit, J., Neumeister, P., Novikoff, P. M., Brownlee, M., Scherer, P. E., Jones, J. G., Whitney, K. D., Donehower, L. A., Harris, E. L., Rohan, T., Johns, D. C., Pestell, R. G. (2003). Cyclin D1 Repression of Peroxisome Proliferator-Activated Receptor {gamma} Expression and Transactivation. Mol. Cell. Biol. 23: 6159-6173 [Abstract] [Full Text]  
  • Yoshikawa, T., Ide, T., Shimano, H., Yahagi, N., Amemiya-Kudo, M., Matsuzaka, T., Yatoh, S., Kitamine, T., Okazaki, H., Tamura, Y., Sekiya, M., Takahashi, A., Hasty, A. H., Sato, R., Sone, H., Osuga, J.-i., Ishibashi, S., Yamada, N. (2003). Cross-Talk between Peroxisome Proliferator-Activated Receptor (PPAR) {alpha} and Liver X Receptor (LXR) in Nutritional Regulation of Fatty Acid Metabolism. I. PPARs Suppress Sterol Regulatory Element Binding Protein-1c Promoter through Inhibition of LXR Signaling. Mol. Endocrinol. 17: 1240-1254 [Abstract] [Full Text]  
  • Nishizuka, M., Arimoto, E., Tsuchiya, T., Nishihara, T., Imagawa, M. (2003). Crucial Role of TCL/TC10beta L, a Subfamily of Rho GTPase, in Adipocyte Differentiation. J. Biol. Chem. 278: 15279-15284 [Abstract] [Full Text]  
  • Kolehmainen, M., Uusitupa, M. I. J., Alhava, E., Laakso, M., Vidal, H. (2003). Effect of the Pro12Ala Polymorphism in the Peroxisome Proliferator-Activated Receptor (PPAR) {gamma}2 Gene on the Expression of PPAR{gamma} Target Genes in Adipose Tissue of Massively Obese Subjects. J. Clin. Endocrinol. Metab. 88: 1717-1722 [Abstract] [Full Text]  
  • Colombo, C., Haluzik, M., Cutson, J. J., Dietz, K. R., Marcus-Samuels, B., Vinson, C., Gavrilova, O., Reitman, M. L. (2003). Opposite Effects of Background Genotype on Muscle and Liver Insulin Sensitivity of Lipoatrophic Mice. ROLE OF TRIGLYCERIDE CLEARANCE. J. Biol. Chem. 278: 3992-3999 [Abstract] [Full Text]  
  • Banerjee, S. S., Feinberg, M. W., Watanabe, M., Gray, S., Haspel, R. L., Denkinger, D. J., Kawahara, R., Hauner, H., Jain, M. K. (2003). The Kruppel-like Factor KLF2 Inhibits Peroxisome Proliferator-activated Receptor-gamma Expression and Adipogenesis. J. Biol. Chem. 278: 2581-2584 [Abstract] [Full Text]  
  • Liberg, D., Sigvardsson, M., Akerblad, P. (2002). The EBF/Olf/Collier Family of Transcription Factors: Regulators of Differentiation in Cells Originating from All Three Embryonal Germ Layers. Mol. Cell. Biol. 22: 8389-8397 [Full Text]  
  • Rondinone, C. M., Trevillyan, J. M., Clampit, J., Gum, R. J., Berg, C., Kroeger, P., Frost, L., Zinker, B. A., Reilly, R., Ulrich, R., Butler, M., Monia, B. P., Jirousek, M. R., Waring, J. F. (2002). Protein Tyrosine Phosphatase 1B Reduction Regulates Adiposity and Expression of Genes Involved in Lipogenesis. Diabetes 51: 2405-2411 [Abstract] [Full Text]  
  • Nanbu-Wakao, R., Morikawa, Y., Matsumura, I., Masuho, Y., Muramatsu, M.-a., Senba, E., Wakao, H. (2002). Stimulation of 3T3-L1 Adipogenesis by Signal Transducer and Activator of Transcription 5. Mol. Endocrinol. 16: 1565-1576 [Abstract] [Full Text]  
  • Han, J., Farmer, S. R., Kirkland, J. L., Corkey, B. E., Yoon, R., Pirtskhalava, T., Ido, Y., Guo, W. (2002). Octanoate Attenuates Adipogenesis in 3T3-L1 Preadipocytes. J. Nutr. 132: 904-910 [Abstract] [Full Text]  
  • Sewter, C., Berger, D., Considine, R. V., Medina, G., Rochford, J., Ciaraldi, T., Henry, R., Dohm, L., Flier, J. S., O'Rahilly, S., Vidal-Puig, A. J. (2002). Human Obesity and Type 2 Diabetes Are Associated With Alterations in SREBP1 Isoform Expression That Are Reproduced Ex Vivo by Tumor Necrosis Factor-{alpha}. Diabetes 51: 1035-1041 [Abstract] [Full Text]  
  • Croissandeau, G., Basak, A., Seidah, N. G., Chretien, M., Mbikay, M. (2002). Proprotein convertases are important mediators of the adipocyte differentiation of mouse 3T3-L1 cells. J. Cell Sci. 115: 1203-1211 [Abstract] [Full Text]  
  • Yu, X., Mertz, J. E. (2001). Critical Roles of Nuclear Receptor Response Elements in Replication of Hepatitis B Virus. J. Virol. 75: 11354-11364 [Abstract] [Full Text]  
  • Caron, M., Auclair, M., Vigouroux, C., Glorian, M., Forest, C., Capeau, J. (2001). The HIV Protease Inhibitor Indinavir Impairs Sterol Regulatory Element-Binding Protein-1 Intranuclear Localization, Inhibits Preadipocyte Differentiation, and Induces Insulin Resistance. Diabetes 50: 1378-1388 [Abstract] [Full Text]  
  • Rodriguez, C., Martinez-Gonzalez, J., Sanchez-Gomez, S., Badimon, L. (2001). LDL Downregulates CYP51 in Porcine Vascular Endothelial Cells and in the Arterial Wall Through a Sterol Regulatory Element Binding Protein-2-Dependent Mechanism. Circ. Res. 88: 268-274 [Abstract] [Full Text]  
  • Zeghari, N., Vidal, H., Younsi, M., Ziegler, O., Drouin, P., Donner, M. (2000). Adipocyte membrane phospholipids and PPAR-gamma expression in obese women: relationship to hyperinsulinemia. Am. J. Physiol. Endocrinol. Metab. 279: E736-E743 [Abstract] [Full Text]  
  • Rosen, E. D., Walkey, C. J., Puigserver, P., Spiegelman, B. M. (2000). Transcriptional regulation of adipogenesis. Genes Dev. 14: 1293-1307 [Full Text]  
  • Tobin, K. A. R., Steineger, H. H., Alberti, S., Spydevold, O., Auwerx, J., Gustafsson, J.-A., Nebb, H. I. (2000). Cross-Talk between Fatty Acid and Cholesterol Metabolism Mediated by Liver X Receptor-{alpha}. Mol. Endocrinol. 14: 741-752 [Abstract] [Full Text]  
  • Flier, J. S., Hollenberg, A. N. (1999). ADD-1 provides major new insight into the mechanism of insulin action. Proc. Natl. Acad. Sci. USA 96: 14191-14192 [Full Text]  
  • Desvergne, B., Wahli, W. (1999). Peroxisome Proliferator-Activated Receptors: Nuclear Control of Metabolism. Endocr. Rev. 20: 649-688 [Abstract] [Full Text]  
  • Hamm, J. K., Park, B. H., Farmer, S. R. (2001). A Role for C/EBPbeta in Regulating Peroxisome Proliferator-activated Receptor gamma Activity during Adipogenesis in 3T3-L1 Preadipocytes. J. Biol. Chem. 276: 18464-18471 [Abstract] [Full Text]  

This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
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 arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Fajas, L.
Right arrow Articles by Auwerx, J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Fajas, L.
Right arrow Articles by Auwerx, J.

Copyright © 2009 by the American Society for Microbiology.   For an alternate route to Journals.ASM.org, visit: http://intl-journals.asm.org | More Info»