A mutation in the c-Fos gene associated with congenital generalized lipodystrophy
- Birgit Knebel†1,
- Jorg Kotzka†1,
- Stefan Lehr1,
- Sonja Hartwig1,
- Haluk Avci1,
- Sylvia Jacob1,
- Ulrike Nitzgen1,
- Martina Schiller1,
- Winfried März2, 3,
- Michael M Hoffmann4, 5,
- Eva Seemanova6,
- Jutta Haas7 and
- Dirk Muller-Wieland7Email author
© Knebel et al.; licensee BioMed Central Ltd. 2013
Received: 7 May 2013
Accepted: 1 August 2013
Published: 7 August 2013
Congenital generalized lipodystrophy (CGL) or Berardinelli–Seip congenital lipodystrophy (BSCL) is a rare genetic syndrome characterized by the absence of adipose tissue. As CGL is thought to be related to malfunctions in adipocyte development, genes involved in the mechanisms of adipocyte biology and maintenance or differentiation of adipocytes, especially transcription factors are candidates. Several genes (BSCL1-4) were found to be associated to the syndrome but not all CGL patients carry mutations in these genes.
Methods and results
In a patient with CGL and insulin resistance we investigated the known candidate genes but the patient did not carry a relevant mutation. Analyses of the insulin activated signal transduction pathways in isolated fibroblasts of the patient revealed a postreceptor defect altering expression of the immediate early gene c-fos. Sequence analyses revealed a novel homozygous point mutation (c.–439, T→A) in the patients’ c-fos promoter. The point mutation was located upstream of the well characterized promoter elements in a region with no homology to any known cis-elements. The identified mutation was not detected in a total of n=319 non lipodystrophic probands. In vitro analyses revealed that the mutation facilitates the formation of a novel and specific protein/DNA complex. Using mass spectrometry we identified the proteins of this novel complex. Cellular investigations demonstrate that the wild type c-fos promoter can reconstitute the signaling defect in the patient, excluding further upstream signaling alterations, and vice versa the investigations with the c-fos promoter containing the identified mutation generally reduce basal and inducible c-fos transcription activity. As a consequence of the identified point mutation gene expression including c-Fos targeted genes is significantly altered, shown exemplified in cells of the patient.
The immediate-early gene c-fos is one essential transcription factor to initiate adipocyte differentiation. According to the role of c-fos in adipocyte differentiation our findings of a mutation that initiates a repression mechanism at c-fos promoter features the hypothesis that diminished c-fos expression might play a role in CGL by interfering with adipocyte development.
Lipodystrophy can be acquired or inherited and results in partially or complete loss of adipose tissue. In the most severe form, congenital generalized lipodystrophy (CGL) or Berardinelli–Seip congenital lipodystrophy (BSCL), total absence of adipose tissue is associated with altered development, fatty liver, muscular hypertrophy, hypertriglyceridemia, acanthosis nigricans, hyperinsulinism and type-2-diabetes [1, 2].
CGL is rare with estimated 1:10 million births and thought to be a genetic syndrome with autosomal recessive trait . In humans several candidate genes (BSCL1-4) were found to be associated to the syndrome [1, 3]. BSCL1/AGPAT2 and BSCL2/seipin are identified in the majority of CGL patients. In single families BSCL3/caveolin-1 and BSCL4/PTRF-Cavin were identified. The BSCL genes are part of mechanisms involved in the adipocyte formation and growth including lipid droplet formation vesicle transport or and glycerophospholipid synthesis . Thus CGL have been valuable models for the identification of new genetic loci involved in development, distribution and plasticity of white fat cells. Although patients are rare and an estimated 1 of 4 existing cases has been included into studies, not all individuals identified bare mutations in these target genes .
Lipodystrophy resemble syndromes of disturbed adipocyte biology or metabolism but the severe congenital forms are thought to be related to malfunctions in adipocyte development [4, 5]. Therefore genes involved in the differentiation of adipocytes, especially transcription factors, are hot candidates. Prominent examples are PPARγ, SREBP-1c in HIV therapy and SREBP-1c or C/EBP in mouse models causing lipodystrophy [2, 4–8]. Another potential candidate is the transcription factor c-Fos a member of the AP-1 complex that is essential to initiate adipocyte differentiation. Accompanied with peak c-fos gene expression a sequential gene expression cascade of specific transcription factors necessary in adipocyte development is temporarily initiated leading to fully differentiated adipocytes [9, 10]. C-fos has been proven to be essential in this transcriptional activation and knockdown of c-fos abolished the ongoing differentiation process .
Since a mutation in the known BSCL genes have not been found a patient with CGL and insulin resistance we examined insulin signaling as central metabolic signal transduction pathways and show the identification of a homozygous point mutation in the c-fos promoter (c.–439, T→A) in this patient. This mutation causes a novel protein/DNA complex which ubiquitously lowers basal and inducible c-fos promoter activity. According to the role of c-fos in adipocyte differentiation our investigations provoke the hypothesis that diminished c-fos expression interferes with adipocyte development and might play a role in CGL.
Fibroblasts initiated from skin biopsies of patient and healthy caucasian volunteer controls were expanded for 4 cycles and stored in liquid nitrogen. Cells were recultured (DMEM, 10% FCS; Life Technologies, Darmstadt, Germany) and expanded for a maximum of 3 passages before harvesting. For exogenous stimulation fibroblasts were grown to 70% confluence and serum starved (1% FCS) for 40 h (quiescent fibroblasts indicated as basal in figure legends) prior to induction with 10-7 M insulin, 10-8 M IGF-1, 1.5×10-8 EGF or 3.3×10-9 M PDGF. Preadipocytes (3T3-L1) and muscle cells (A7r5) were cultured in DMEM and liver cells (HepG2) in RPMI 1640 (Life Technologies) supplemented with 10% FCS. Institutional research ethics approval (PV3641) in line with the Helsinki Declaration was obtained for this study.
Nuclear extracts from fibroblasts of the patient and controls, or HepG2 cells were prepared as described .
Insulin induced signal transduction
MAPK activity assays and western blotting with polyclonal anti-Akt or anti-phospho Akt antibody (New England Biolabs, Frankfurt, Germany) or polyclonal anti-MAPK antibody (BD Transduction; Heidelberg, Germany) were performed as described .
Real-time (RT) PCR
Total RNA was extracted with RNeasy Mini Spin Kit (Qiagen, Hilden, Germany). RT- PCR analyses were performed in triplicates with c-fos gene-specific probes and 18S RNA internal standard (Applied Biosystems, Darmstadt, Germany) as described . Expression results were determined as relative RNA amounts of target.
Plasmid constructs for transient transfection of primary fibroblasts
C-fos promoter (nt −734 to +43; numbering based on TS (=1) according to K00650) was PCR amplified from genomic DNA of controls and patient using following primers: -734 to −712: 5’-GCGAGGAACAGTGCTAGTATTGCT-3’/ +43 to +12: 5’-CGGCTCAGTCTTGGCTTCTCAGTTGCTCGCT-3’. Wild type c-fos promoter fragment and the corresponding fragment of the patient were inserted in sense orientation into pGL3basic vector (Promega, Mannheim, Germany) to bring the reporter gene luciferase under control of wild type c-fos promoter (pc-fos-wt) or the mutated promoter (pc-fos -439T>A). The expression vector pFA-Elk-1 containing the regulative domains of transcription factor Elk-1 (aa 307 to 427) fused to the heterologous DNA binding domains of Gal4 (aa 1 to 147) under control of a MLV-promoter was used (Life Technologies). For monitoring transactivation the reporter plasmid pGal4-Luc5 containing the luciferase gene under control of 5× Gal4 binding elements was cotransfected in these experiments (Life Technologies). As reference of transfection efficiency the β-galactosidase expression vector pEF-ßGal was used. Independent plasmid preparations and cells were used for replicate experiments.
Cell suspensions (2×105 cells/well) of 3T3-L1, A7r5, HepG2 cells or fibroblasts of patient and control were mixed with vectors as indicated in figure legends and pulsed for 18 msec (3T3-L1, A7r5, HepG2) or 9 msec (fibroblasts). For exogenous induction, cells were serum-starved on day one following transfection for 40 h and incubated with 10-7M insulin or 3.3×10-9M PDGF for 3 h before harvesting. Transfection, monitoring of transfection efficiency and luciferase assays were performed as described .
Direct sequence analyses
Genomic DNA was extracted from fibroblasts of patient or control using the Qiagen blood kit™. For reevaluation of the identified mutation only limited amounts of genomic DNA of the patient’s parents but no biopsies were available. The coding sequence of AGPAT2 (NM_006412.3), caveolin-1 (NM_001753.4; NM_001172895.1), seipin (NM_001122955.3), CAV/PTFR (NM_012232) and c-fos promoter (K00650) were analyzed by direct sequencing (ABI PRISM 3100, Applied Biosystems).
Restriction analyses for the identified c-fos promoter mutation
Genomic DNA of 319 unrelated caucasian subjects was isolated from PMBCs and c-fos promoter (−603 to +12) was amplified (−603 to −579: 5’ primer: 5’-AGGCTTAAGTCCTCGGGGTCCTGT-3’; +43 to +12: 3’ primer: 5’-CGGCTCAGTCTTGGCTTCTCAGTTGCTCGCT-3’). PCR products were reamplified with a mutated primer (−441: C>A) introducing a Tsp509I restriction site solely in wild type c-fos promoter (5’ primer: -470 to −440, c-fos mut −441: C>A: 5’-CATTGAACCAGGTGCGAATGTTCTCTCTA A-3‘ and 3‘ primer −337 to −307: 5’-AGATGTCCTAATATGGACATCCTGTGTAAG-3’). PCR products were Tsp509I digested and size fractionated. Genomic DNA of patient was always treated in parallel for control. 10% of samples were randomly chosen to confirm results by direct sequencing.
DNaseI protection analyses
Footprinting analyses were performed using the sure track footprinting kit™ (GE Healthcare, Munich, Germany). Promoter fragments (nt −462 to −325) were isolated from pc-fos-wt or pc-fos-patient by EcoRI/EcoNI restriction and cohesive ends were labeled with 20 μCi [α32P] dATP and Klenow fragment. 100.000 cpm of radiolabeled fragments were incubated with increasing concentrations of nuclear extracts (4 μg, 8 μg, 20 μg, 40 μg) from human liver cells (HepG2) and subsequently digested for 1 min with different concentrations of DNaseI (0.11U, 0.33U, 1.0U). Reactions were terminated and deproteinized by LiCl precipitation. DNA fragments were precipitated and separated on an 8% PAGE containing 7 M urea. Purine nucleotide sequence ladders from the EcoRI/EcoNI promoter fragments were loaded in parallel to confirm sequence of protected areas.
Electrophoretic mobility shift assay (EMSA)
EMSA were performed according to  and reactions were analyzed on 5% non-denaturating PAGE. For analyses of the in vitro ternary complex formation with nuclear extracts of fibroblasts from control or the patient, 2 pmol sre-element promoter fragments (−331 to −280 5’CCCCTTACACGGATGTCCATATTAGGACATCTGCGTCAGCAGGTTTCCACG; 3’GGAATGTGCCTACAGGTAATAATCCTGTAGACGCAGTCGTCCAAAGGTGCCC) were labeled with 20 μCi [α32P]dGTP using 5U Klenow fragment, prior to use. For completion experiments 100- or 10-fold molar excess of unlabeled sre fragments or unspecific SP-1 promoter fragment (5’-GTTAGGGGCGGGATGGGCGGAGTT -3’) were used.
Analyses of the novel protein/DNA interaction at the c-fos promoter were performed with c-fos-wt (−451 to −431: 5’-TGTTCTCTCTCATTCTGCGCCG-3’) or c-fos-patient (−451 to −431, -439T>A: 5’-TGTTCTCTCTCAA TCTGCGCCG-3’) endlabeled with 5U PNK and 20 μCi [γ32P]dATP, prior to use. For competition experiments 10× or 100× unlabeled c-fos-wt or pc-fos-patient fragment were used. Experiments were performed with nuclear extracts (5 μg) of human liver cells (HepG2).
Protein identification of protein/DNA complex proteins by MALDI-MS
For preparative EMSA a Cy3-labeled c-fos-patient fragment was used in the procedure. Gels were scanned using a Typhoon scanner (GE, Freiburg, Germany) and fluorescence marked bands were cut from gels. The gel slices were placed on a 10% SDS-PAGE for separation of complex proteins. Four independent EMSA replicates were performed and cutted protein/DNA complex were separated on four SDS-PAGE each. Of all protein bands three different punch samples were excised and subjected to mass spectrometry analyses according to  for identification. Acquired mass spectra (peptide mass fingerprint) were automatically calibrated and annotated using Compass 1.3 software and xml formatted peak lists were transferred to Proteinscape3.0 (Bruker Daltonik, Bremen Germany). MS peptide mass fingerprint were used to search a human sub-set of Swiss-Prot (Sprot_2011; 20249 20401 protein entries) non-redundant database using Mascot search engine (Version 2.2, Matrix Science Ltd, London, UK) Mass tolerance was set to 50 ppm for peptide spectra and a combined mascot score over 70 was taken significant (p < 0.01). For verifying the results each protein spot was picked and identified from at least three physically different gels.
Affymetrix chip expression analyses: identification of differentially regulated transcripts independent to individual expression variation
Fibroblasts of patient and 6 individual controls were cultured to passage 6 each. Four replicate analyses of patient cells (initiated from two primary stored cell pools) and 6 individual controls (initiated from one primary stored cell pool each) were used. Equal amounts of total RNA were processed according to the GeneChip One-Cycle eukaryotic Target Labeling Assay (GeneChip Expression analysis technical Manual, http://www.affymetrix.com/support/Technical/manual/expression_manual.affx) and used for expression analyses with Hu95A_v2 Arrays (Affymetrix UK Ltd). Syntheses of cRNA and fragmentation were quality controlled and monitored with a RNA 6000 nano kit (Agilent, Taufkirchen, Germany). Detection of probe sets was performed using a GeneChip scanner (GCOS 1.4 package, Affymetrix). The original CEL files were directly implemented into Genespring 12.0 (Agilent) for analyses. The Genespring 12.0 Volcano Plot analyses workflow with default settings (paired t-test, multiple testing correction: Benjamini-Hochberg) of the gene expression data sets were used to identify genes with statistic significant expression (p < 0.05) and a minimum 1.5-fold difference among conditions. Full data sets are available under accession number GSE39825 (http://www.ncbi.nlm.nih.gov/geo/).
Web based functional annotation of differentially expressed genes and identified proteins
For functional annotation and conserved promoter element site search web based tools were used (http://david.abcc.ncifcrf.gov/) [15, 16]. For functional annotation protein IDs or Affymetrix IDs, fold change, and t-test p-value of detection significance were imported to Ingenuity Pathway Analysis (IPA) System (http://www.ingenuity.com). IPA was carried out with p < 0.002 as cutoff point. Pathways indicating altered transcriptional regulation were deduced from fold change differences observed.
Data are given as means ± S.D. Students t-test was used to determine statistical significance.
Patient characteristic and genetics
The female caucasian patient was born at term with reduced birth weight (2,950 g). The parents were healthy, not consanguineous and gave birth to four further healthy children. At age of one year the patient retrieved to thrive and beginning lipodystrophy was diagnosed. Pronounced acanthosis nigricans was observed, being a hint for altered insulin signaling. Until the age of five years prediabetes, progressive hepatomegaly and lipoatrophy appeared with complete loss of adipose tissue. Physical examination revealed generalized decreased subcutaneous adipose tissue, distended abdomen with enlarged palpable liver and growth retardation from 10% (1 year) to 75% (7 years) of normal range. The patient had the typical appearance of congenital generalized lipodystrophy including hypertrichiosis, hepatomegaly, splenomegaly, but no mental retardation. The patient had marked muscularity probably due to missing subcutaneous adipose tissue. The main known candidate genes associated with congenital generalized lipodystrophy, i.e. BSCL1/AGPAT2, BSCL2/seipin, BSCL3/caveolin-1 and BSCL4/PRTF were analyzed. No sequence alteration specific for the lipodystrophic phenotype was identified (data not shown). At age of five years laboratory analyses showed elevated plasma cholesterol levels (450 mg/dl) and modestly elevated triglycerides (218 mg/dl). Glucose intolerance detected by oGTT showed an increase of blood glucose levels from 103 mg/dl (normal range 65 to 100 mg/dl) up to 176 mg/dl (normal range 80 to 126 mg/dl) and plasma insulin levels from 96 mU/l to 276 mU/l, respectively, indicating insulin resistance. The patient died at the age of eight during a hyper acute varicella infection as primary cause of death. An autopsy was not performed.
Insulin mediated transcriptionally activation of the c-fos gene
As the patient was the only known case of lipodystrophy in the family nothing remained but analyzing a possible defect in insulin signaling, we characterized known signaling pathways. For this purpose we utilized primary fibroblasts initiated from skin biopsies.
Identification of a point mutation in c-fos promoter causing a novel specific protein/DNA interaction
Functional annotation of proteins identified in the novel DNA binding complex
Structure-specific DNA binding
Adenyl ribonucleotide binding
Adenyl nucleotide binding
Purine nucleotide binding
ATP-dependent helicase activity
Purine NTP-dependent helicase activity
Double-stranded telomeric DNA binding
Protein C-terminus binding
Sequence-specific DNA binding
ATP-dependent DNA helicase activity
Single-stranded RNA binding
DNA helicase activity
Single-stranded DNA binding
DNA-dependent ATPase activity
Double-stranded DNA binding
The point mutation c.–439 T→A in the 5’UTR of c-fos gene results in ubiquitous impairment of c-fos promoter activity
Biological relevance of reduced basal and inducible c-fos expression
Implication of the mutation (c.–439 T→A) in the promoter of c-fos gene
Congenital lipodystrophy is characterized by the complete loss of adipose tissue. In our patient with CGL we identified a homozygous de novo point mutation in the c-fos promoter. Although this is an unexpected finding, increasing genomic information indicated that approximately 50–100 germ line de novo mutations can occur in each individual . Nevertheless, the mutation identified in this study has a clear functional relevance of c-fos promoter activity. Due to the identified mutation a novel mutation-specific protein/DNA interaction is formed. As consequence basal and inducible c-fos expression is ubiquitously lowered. The proteins identified in the complex represent no classical DNA interacting proteins but DNA modifying helicases, nuclear ribonucleoproteins (hnRP), structural proteins, and heat shock proteins. It was shown that the single strand binding ATP dependent helicases are involved in telomere maintenance, double strand breaking repair and DNA unwinding as needed to transcriptional activation, especially it has long been noted that UV initiated DNA damage interferes with inducibility of c-fos expression and UV induced DNA damage interferes with adipocyte differentiation [20, 21]. HnRPs localized to the nucleus are involved in transcriptional repression processes including c-fos mRNA transcription . Furthermore nuclear actin or nucleolin are involved in chromatin-remodeling processes and actin can be associated to hnRNPs A/B type family as also shown here [23, 24]. Such modifications in chromatin structure are required for gene expression and adipocyte differentiation as local chromatin remodeling has been described in the regulation of the PPARγ transcription during adipocyte differentiation [25, 26].
All together the novel protein complex seems to act on c-fos promoter as ubiquitous transcriptional repressor. Mechanistically one can speculate that the complex alters DNA packaging, masks basal or activating promoter elements or interacts with transcription factors. The novel protein DNA complex identified might constitutively mimic a transcriptional repression process that usually is under tight regulation in cells .
The consequence of lowering c-fos expression is a differential gene expression pattern in our patient compared to controls. Further analyses shows that the reduced c-fos expression affects genes involved in multiple metabolic pathways, transcriptional control and a large fraction of genes involved in cell cycle control and differentiation processes most of them AP-1 dependent. Of special note are genes involved in adipocyte differentiation as Wnt5A, IL6, FGF-2, ODC-1, C/EBP, NR2F2, INHBB, SFRP1 or ITGA6. On the other hand gene functional annotation revealed that genes differentially expressed are also regulated by various adipose differentiation transcription factors as C/EBPs, PPARs or the SREBP family.
Can the reduced c-fos promoter activity be related to CGL?
On cellular level the point mutation identified in our patient and the binding of the novel protein complex results in reduced basal as well as inducible c-fos expression but not complete loss of c-fos expression. This reduced c-fos expression influences expression on many other genes. This might be due to the fact that c-Fos doesn’t act as single transcription factor but is part of AP-1 complex. This protein complex consists of a combination of two proteins from various homologues proteins of Jun, ATF, MAF and Fos families, i.e. c-jun, JUNB, JUND, ATF2, ATF3/LRF1, B-ATF, JDP1, JDP2, c-Maf, MafB, MafA, MafG/F/K, Nrl, c-fos, Fra-1, Fra-2, FOSL or FosB. As consequence depending on dimer composition the transactivation activity of AP-1 complex varies from activation to repression of the target gene transactivation activity . Furthermore, the occupancy of AP-1 sites by AP-1 transcription complex also influences transcription of overlapping or adjacent promoter elements. The direct competition of AP-1 to binding site CRE or ARE has been reported [27, 28]. Knockout mice deficient for c-Fos revealed phenotypes with severe osteopetrosis and altered hematopoiesis. They show reduced fetal and placental weight, reduced weight gain and reduced fat mass, but to our knowledge there are no studies assessing further metabolic parameters [29–31]. However there is a reciprocal interaction between bone and energy metabolism . Osteoblasts and adipocytes originate from a common mesenchymal progenitor and specific differentiation via BMPs and WNT pathways determine the cell fate to bone or adipose specific precursor cells . This speculation is supported by mice overexpressing Fra-1 which develop lipodystrophy due to reduced adipocyte differentiation via C/EBPa inhibition and transcriptional repression . Interestingly, patients with congenital lipodystrophy show increased bone age and density, enlarged epiphyses, sclerotic skeletons and alterations in dentition . Furthermore the promoter activation of the immediately early gene c-fos is involved in various signaling cascades. One of those is IGF-1 signaling, that shares the signaling cascade and activation mechanisms of c-fos promoter as insulin . As the role of IGF-1 and the GH/IGF-1 axis in various syndromes with growth restriction is well established  one can speculate that the growth alterations or skin and hair variations observed in the patient are most likely a consequence of interference with IGF-1 signaling.
We thank the German Ministry of Education and Research (BMBF/01KS9502) and the Köln Fortune Program/Faculty of Medicine, University of Cologne, and the German Diabetes Center, Duesseldorf and the LiDia program of City of Hamburg for support.
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