Transcriptional regulation of white adipocyte differentiation (Homo sapiens)

From WikiPathways

Revision as of 08:28, 17 July 2014 by ReactomeTeam (Talk | contribs)
Jump to: navigation, search
8, 9, 11, 12, 14...7, 8, 25, 28, 32111128111, 10, 36, 4128112, 132827, 29, 344, 17, 33, 403, 28, 328, 282818, 22, 281116PPARA: Fatty AcidComplex (ActivatedPPARA) [nucleoplasm]PPARG:RXRAHeterodimer[nucleoplasm]PPARG:FattyAcid:RXRA:Mediator:CoactivatorComplex[nucleoplasm]GLUT4 tetramer[plasma membrane]Ligands of PPARG[nucleoplasm]FABP4:Ligands ofPPARG [nucleoplasm]nucleoplasmLigands of PPARA[nucleoplasm]NF-kB complex[nucleoplasm]lipid particleLigands of PPARG[nucleoplasm]PPARG:RXRA:CorepressorComplex[nucleoplasm]Coactivators ofPPARalpha[nucleoplasm]Mediator Complex(consensus)[nucleoplasm]Activated PPARA:RXRAHeterodimer[nucleoplasm]Activated PPARG:RXRA[nucleoplasm]PPARG:Fatty AcidLigand [nucleoplasm]cytosolPPARG:RXRAHeterodimer[nucleoplasm]Mediator Complex(consensus)[nucleoplasm]PPARA:RXRACoactivator Complex[nucleoplasm]NCOA1 [nucleoplasm]MED25 [nucleoplasm]CDK19 [nucleoplasm]RGZ [nucleoplasm]CHD9 [nucleoplasm]MED6 [nucleoplasm]RXRAMED1 [nucleoplasm]MED25 [nucleoplasm]ANGPTL4PPARG [nucleoplasm]MED13L [nucleoplasm]MED7 [nucleoplasm]NCOA1MED13 [nucleoplasm]SMARCD3[nucleoplasm]CCNC [nucleoplasm]MED18 [nucleoplasm]MED7 [nucleoplasm]CDK19 [nucleoplasm]LEPPalm [nucleoplasm]MED9 [nucleoplasm]CDK8 [nucleoplasm]MED16 [nucleoplasm]MED10(2-135)[nucleoplasm]NCOA3 [nucleoplasm]CEBPBMED14 [nucleoplasm]MED27 [nucleoplasm]MED13L [nucleoplasm]Actos [nucleoplasm]MED23 [nucleoplasm]HELZ2 [nucleoplasm]GLUT4 tetramerMED24 [nucleoplasm]RXRA [nucleoplasm]RGZ [nucleoplasm]MED26 [nucleoplasm]MED26 [nucleoplasm]13(S')-HODE[nucleoplasm]PPARA:RXRACoactivator ComplexNF-kB complexMED21 [nucleoplasm]HDAC3 [nucleoplasm]MED31 [nucleoplasm]CREBBP(2-2442)[nucleoplasm]SREBF1A,2MED17 [nucleoplasm]LINA [nucleoplasm]ALA [nucleoplasm]MED11 [nucleoplasm]CREBBP(2-2442)[nucleoplasm]PPARG:FattyAcid:RXRA:Mediator:CoactivatorComplex9S-HODE[nucleoplasm]MED10(2-135)[nucleoplasm]MED6 [nucleoplasm]MED4 [nucleoplasm]Mediator Complex(consensus)WNT1,WNT10B9S-HODE[nucleoplasm]MED20 [nucleoplasm]TGFB1(279-390)MED4 [nucleoplasm]NCOR1 [nucleoplasm]CDK4(2-303)PPARG [nucleoplasm]SLC2A4 [plasmamembrane]13(S')-HODE[nucleoplasm]MED30(1-178)[nucleoplasm]LPLMED9 [nucleoplasm]MED16 [nucleoplasm]FABP4MED12 [nucleoplasm]RXRA [nucleoplasm]MED1 [nucleoplasm]PPARGC1A[nucleoplasm]FABP4:Ligands ofPPARGAA [nucleoplasm]NR2F2NCOA2 [nucleoplasm]MED19 [nucleoplasm]MED13 [nucleoplasm]MED15 [nucleoplasm]EP300(1-2414)[nucleoplasm]CARM1(2-608)[nucleoplasm]MED1 [nucleoplasm]CEBPARXRA [nucleoplasm]KLF4NCOA3CCND3NCOR1MED31 [nucleoplasm]PPARA [nucleoplasm]CDK8 [nucleoplasm]MED24 [nucleoplasm]PPARG:RXRA:CorepressorComplexEGR2PPARG:RXRAHeterodimerMED22 [nucleoplasm]HELZ2 [nucleoplasm]RELA [nucleoplasm]EBF1HDAC3PPARGNFKB1(1-433)[nucleoplasm]MED12 [nucleoplasm]MED8 [nucleoplasm]FABP4 [nucleoplasm]NCOA6 [nucleoplasm]PCK1NCOA1 [nucleoplasm]MED8 [nucleoplasm]MED11 [nucleoplasm]PPARGC1AHELZ2PPARG [nucleoplasm]NCOA2TNF(77-233)PLIN1NCOA2 [nucleoplasm]MED18 [nucleoplasm]MED23 [nucleoplasm]CREBBP(2-2442)MED22 [nucleoplasm]MED30(1-178)[nucleoplasm]NCOR2 [nucleoplasm]MED29(2-200)[nucleoplasm]CEBPDMED27 [nucleoplasm]KLF5EP300(1-2414)MED20 [nucleoplasm]FABP4RXRA [nucleoplasm]EPA [nucleoplasm]MED15 [nucleoplasm]TBL1XR1[nucleoplasm]MED17 [nucleoplasm]Actos [nucleoplasm]MED19 [nucleoplasm]4xPalmC-CD36TGS1 [nucleoplasm]ADIPOQMED29(2-200)[nucleoplasm]CCNC [nucleoplasm]MED21 [nucleoplasm]TBL1X [nucleoplasm]NCOR2MED14 [nucleoplasm]65, 3726195, 37


Description

Adipogenesis is the process of cell differentiation by which preadipocytes become adipocytes. During this process the preadipocytes cease to proliferate, begin to accumulate lipid droplets and develop morphologic and biochemical characteristics of mature adipocytes such as hormone responsive lipogenenic and lipolytic programs. The most intensively studied model system for adipogenesis is differentiation of the mouse 3T3-L1 preadipocyte cell line by an induction cocktail of containing mitogens (insulin/IGF1), glucocorticoid (dexamethasone), an inducer of cAMP (IBMX), and fetal serum (Cao et al. 1991, reviewed in Farmer 2006). More recently additional cellular models have become available to study adipogenesis that involve almost all stages of development (reviewed in Rosen and MacDougald 2006). In vivo knockout mice lacking putative adipogenic factors have also been extensively studied. Human pathways are traditionally inferred from those discovered in mouse but are now beginning to be validated in cellular models derived from human adipose progenitors (Fischer-Posovszky et al. 2008, Wdziekonski et al. 2011).
Adipogenesis is controlled by a cascade of transcription factors (Yeh et al. 1995, reviewed in Farmer 2006, Gesta et al. 2007). One of the first observable events during adipocyte differentiation is a transient increase in expression of the CEBPB (CCAAT/Enhancer Binding Protein Beta, C/EBPB) and CEBPD (C/EBPD) transcription factors (Cao et al. 1991, reviewed in Lane et al. 1999). This occurs prior to the accumulation of lipid droplets. However, it is the subsequent inductions of CEBPA and PPARG that are critical for morphological, biochemical and functional adipocytes.
Ectopic expression of CEBPB alone is capable of inducing substantial adipocyte differentiation in fibroblasts while CEBPD has a minimal effect. CEBPB is upregulated in response to intracellular cAMP (possibly via pCREB) and serum mitogens (possibly via Krox20). CEBPD is upregulated in response to glucocorticoids. The exact mechanisms that upregulate the CEBPs are not fully known.
CEBPB and CEBPD act directly on the Peroxisome Proliferator-activated Receptor Gamma (PPARG) gene by binding its promoter and activating transcription. CEBPB and CEBPD also directly activate the EBF1 gene (and possibly other EBFs) and KLF5 (Jimenez et al. 2007, Oishi 2005). The EBF1 and KLF5 proteins, in turn bind, and activate the PPARG promoter. Other hormones, such as insulin, affect PPARG expression and other transcription factors, such as ADD1/SREBP1c, bind the PPARG promoter. This is an area of ongoing research.
During adipogenesis the PPARG gene is transcribed to yield 2 variants. The adipogenic variant 2 mRNA encodes 30 additional amino acids at the N-terminus compared to the widely expressed variant 1 mRNA.
PPARG encodes a type II nuclear hormone receptor (remains in the nucleus in the absence of ligand) that forms a heterodimer with the Retinoid X Receptor Alpha (RXRA). The heterodimer was initially identified as a complex regulating the aP2/FABP4 gene and named ARF6 (Tontonoz et al. 1994).
The PPARG:RXRA heterodimer binds a recognition sequence that consists of two hexanucleotide motifs (DR1 motifs) separated by 1 nucleotide. Binding occurs even in the absence of ligands, such as fatty acids, that activate PPARG. In the absence of activating ligands, the PPARG:RXRA complex recruits repressors of transcription such as SMRT/NCoR2, NCoR1, and HDAC3 (Tontonoz and Spiegelman 2008).
Each molecule of PPARG can bind 2 molecules of activating ligands. Although, the identity of the endogenous ligands of PPARG is unknown, exogenous activators include fatty acids and the thiazolidinedione class of antidiabetic drugs (reviewed in Berger et al. 2005, Heikkinen et al. 2007, Lemberger et al. 1996). The most potent activators of PPARG in vitro are oxidized derivatives of unsaturated fatty acids.. Upon binding activating ligands PPARG causes a rearrangement of adjacent factors: Corepressors such as SMRT/NCoR2 are lost and coactivators such as TIF2, PRIP, CBP, and p300 are recruited (Tontonoz and Spiegelman). PPARG also binds directly to the TRAP220 subunit of the TRAP/Mediator complex that recruits RNA polymerase II. Thus binding of activating ligand by PPARG causes transcription of PPARG target genes.
Targets of PPARG include genes involved in differentiation (PGAR/HFARP, Perilipin, aP2/FABP4, CEBPA), fatty acid transport (LPL, FAT/CD36), carbohydrate metabolism (PEPCK-C, AQP7, GK, GLUT4), and energy homeostasis (LEPTIN and ADIPONECTIN) (Perera et al. 2006).
Within 10 days of differentiation CEBPB and CEBPD are no longer located at the PPARG promoter. Instead CEBPA is present. EBF1 and PPARG bind the CEBPA promoter and activate transcription of CEBPA, one of the key transcription factors in adipogenesis. A current hypothesis posits a self-reinforcing loop that maintains PPARG expression and the differentiated state: PPARG activates CEBPA and CEBPA activates PPARG. Additionally EBF1 (and possibly other EBFs) activates CEBPA, CEBPA activates EBF1, and EBF1 activates PPARG.Original Pathway at Reactome: http://www.reactome.org/PathwayBrowser/#DB=gk_current&FOCUS_SPECIES_ID=48887&FOCUS_PATHWAY_ID=381340

Try the New WikiPathways

View approved pathways at the new wikipathways.org.

Quality Tags

Ontology Terms

 

Bibliography

View all...
  1. Melzner I, Scott V, Dorsch K, Fischer P, Wabitsch M, Brüderlein S, Hasel C, Möller P.; ''Leptin gene expression in human preadipocytes is switched on by maturation-induced demethylation of distinct CpGs in its proximal promoter.''; PubMed Europe PMC Scholia
  2. Pilch PF, Wilkinson W, Garvey WT, Ciaraldi TP, Hueckstaedt TP, Olefsky JM.; ''Insulin-responsive human adipocytes express two glucose transporter isoforms and target them to different vesicles.''; PubMed Europe PMC Scholia
  3. Tontonoz P, Spiegelman BM.; ''Fat and beyond: the diverse biology of PPARgamma.''; PubMed Europe PMC Scholia
  4. Heikkinen S, Auwerx J, Argmann CA.; ''PPARgamma in human and mouse physiology.''; PubMed Europe PMC Scholia
  5. Itoh T, Fairall L, Amin K, Inaba Y, Szanto A, Balint BL, Nagy L, Yamamoto K, Schwabe JW.; ''Structural basis for the activation of PPARgamma by oxidized fatty acids.''; PubMed Europe PMC Scholia
  6. Paoletti AC, Parmely TJ, Tomomori-Sato C, Sato S, Zhu D, Conaway RC, Conaway JW, Florens L, Washburn MP.; ''Quantitative proteomic analysis of distinct mammalian Mediator complexes using normalized spectral abundance factors.''; PubMed Europe PMC Scholia
  7. Lemberger T, Desvergne B, Wahli W.; ''Peroxisome proliferator-activated receptors: a nuclear receptor signaling pathway in lipid physiology.''; PubMed Europe PMC Scholia
  8. Perera RJ, Marcusson EG, Koo S, Kang X, Kim Y, White N, Dean NM.; ''Identification of novel PPARgamma target genes in primary human adipocytes.''; PubMed Europe PMC Scholia
  9. Chandra V, Huang P, Hamuro Y, Raghuram S, Wang Y, Burris TP, Rastinejad F.; ''Structure of the intact PPAR-gamma-RXR- nuclear receptor complex on DNA.''; PubMed Europe PMC Scholia
  10. Berger JP, Akiyama TE, Meinke PT.; ''PPARs: therapeutic targets for metabolic disease.''; PubMed Europe PMC Scholia
  11. Lane MD, Tang QQ, Jiang MS.; ''Role of the CCAAT enhancer binding proteins (C/EBPs) in adipocyte differentiation.''; PubMed Europe PMC Scholia
  12. Jimenez MA, Akerblad P, Sigvardsson M, Rosen ED.; ''Critical role for Ebf1 and Ebf2 in the adipogenic transcriptional cascade.''; PubMed Europe PMC Scholia
  13. Tao N, Wagner SJ, Lublin DM.; ''CD36 is palmitoylated on both N- and C-terminal cytoplasmic tails.''; PubMed Europe PMC Scholia
  14. Pessin JE, Bell GI.; ''Mammalian facilitative glucose transporter family: structure and molecular regulation.''; PubMed Europe PMC Scholia
  15. Wdziekonski B, Mohsen-Kanson T, Villageois P, Dani C.; ''The generation and the manipulation of human multipotent adipose-derived stem cells.''; PubMed Europe PMC Scholia
  16. Rakhshandehroo M, Hooiveld G, Müller M, Kersten S.; ''Comparative analysis of gene regulation by the transcription factor PPARalpha between mouse and human.''; PubMed Europe PMC Scholia
  17. Sato S, Tomomori-Sato C, Parmely TJ, Florens L, Zybailov B, Swanson SK, Banks CA, Jin J, Cai Y, Washburn MP, Conaway JW, Conaway RC.; ''A set of consensus mammalian mediator subunits identified by multidimensional protein identification technology.''; PubMed Europe PMC Scholia
  18. Rival Y, Stennevin A, Puech L, Rouquette A, Cathala C, Lestienne F, Dupont-Passelaigue E, Patoiseau JF, Wurch T, Junquéro D.; ''Human adipocyte fatty acid-binding protein (aP2) gene promoter-driven reporter assay discriminates nonlipogenic peroxisome proliferator-activated receptor gamma ligands.''; PubMed Europe PMC Scholia
  19. Segawa K, Matsuda M, Fukuhara A, Morita K, Okuno Y, Komuro R, Shimomura I.; ''Identification of a novel distal enhancer in human adiponectin gene.''; PubMed Europe PMC Scholia
  20. Mukherjee R, Jow L, Croston GE, Paterniti JR.; ''Identification, characterization, and tissue distribution of human peroxisome proliferator-activated receptor (PPAR) isoforms PPARgamma2 versus PPARgamma1 and activation with retinoid X receptor agonists and antagonists.''; PubMed Europe PMC Scholia
  21. Sewter CP, Blows F, Vidal-Puig A, O'Rahilly S.; ''Regional differences in the response of human pre-adipocytes to PPARgamma and RXRalpha agonists.''; PubMed Europe PMC Scholia
  22. Lu J, Chen M, Stanley SE, Li E.; ''Effect of heterodimer partner RXRalpha on PPARgamma activation function-2 helix in solution.''; PubMed Europe PMC Scholia
  23. Tontonoz P, Graves RA, Budavari AI, Erdjument-Bromage H, Lui M, Hu E, Tempst P, Spiegelman BM.; ''Adipocyte-specific transcription factor ARF6 is a heterodimeric complex of two nuclear hormone receptors, PPAR gamma and RXR alpha.''; PubMed Europe PMC Scholia
  24. Juge-Aubry C, Pernin A, Favez T, Burger AG, Wahli W, Meier CA, Desvergne B.; ''DNA binding properties of peroxisome proliferator-activated receptor subtypes on various natural peroxisome proliferator response elements. Importance of the 5'-flanking region.''; PubMed Europe PMC Scholia
  25. Boiteux G, Lascombe I, Roche E, Plissonnier ML, Clairotte A, Bittard H, Fauconnet S.; ''A-FABP, a candidate progression marker of human transitional cell carcinoma of the bladder, is differentially regulated by PPAR in urothelial cancer cells.''; PubMed Europe PMC Scholia
  26. De Vos P, Lefebvre AM, Miller SG, Guerre-Millo M, Wong K, Saladin R, Hamann LG, Staels B, Briggs MR, Auwerx J.; ''Thiazolidinediones repress ob gene expression in rodents via activation of peroxisome proliferator-activated receptor gamma.''; PubMed Europe PMC Scholia
  27. Tsai KL, Tomomori-Sato C, Sato S, Conaway RC, Conaway JW, Asturias FJ.; ''Subunit architecture and functional modular rearrangements of the transcriptional mediator complex.''; PubMed Europe PMC Scholia
  28. Lambe KG, Tugwood JD.; ''A human peroxisome-proliferator-activated receptor-gamma is activated by inducers of adipogenesis, including thiazolidinedione drugs.''; PubMed Europe PMC Scholia
  29. Kita A, Yamasaki H, Kuwahara H, Moriuchi A, Fukushima K, Kobayashi M, Fukushima T, Takahashi R, Abiru N, Uotani S, Kawasaki E, Eguchi K.; ''Identification of the promoter region required for human adiponectin gene transcription: Association with CCAAT/enhancer binding protein-beta and tumor necrosis factor-alpha.''; PubMed Europe PMC Scholia
  30. Qiao L, Maclean PS, Schaack J, Orlicky DJ, Darimont C, Pagliassotti M, Friedman JE, Shao J.; ''C/EBPalpha regulates human adiponectin gene transcription through an intronic enhancer.''; PubMed Europe PMC Scholia
  31. Pelton PD, Zhou L, Demarest KT, Burris TP.; ''PPARgamma activation induces the expression of the adipocyte fatty acid binding protein gene in human monocytes.''; PubMed Europe PMC Scholia
  32. Gelman L, Zhou G, Fajas L, Raspé E, Fruchart JC, Auwerx J.; ''p300 interacts with the N- and C-terminal part of PPARgamma2 in a ligand-independent and -dependent manner, respectively.''; PubMed Europe PMC Scholia
  33. Tian L, Zhou J, Casimiro MC, Liang B, Ojeifo JO, Wang M, Hyslop T, Wang C, Pestell RG.; ''Activating peroxisome proliferator-activated receptor gamma mutant promotes tumor growth in vivo by enhancing angiogenesis.''; PubMed Europe PMC Scholia
  34. Knutti D, Kaul A, Kralli A.; ''A tissue-specific coactivator of steroid receptors, identified in a functional genetic screen.''; PubMed Europe PMC Scholia
  35. Rosen ED, MacDougald OA.; ''Adipocyte differentiation from the inside out.''; PubMed Europe PMC Scholia
  36. Oishi Y, Manabe I, Tobe K, Tsushima K, Shindo T, Fujiu K, Nishimura G, Maemura K, Yamauchi T, Kubota N, Suzuki R, Kitamura T, Akira S, Kadowaki T, Nagai R.; ''Krüppel-like transcription factor KLF5 is a key regulator of adipocyte differentiation.''; PubMed Europe PMC Scholia
  37. Miller SG, De Vos P, Guerre-Millo M, Wong K, Hermann T, Staels B, Briggs MR, Auwerx J.; ''The adipocyte specific transcription factor C/EBPalpha modulates human ob gene expression.''; PubMed Europe PMC Scholia
  38. Puigserver P, Wu Z, Park CW, Graves R, Wright M, Spiegelman BM.; ''A cold-inducible coactivator of nuclear receptors linked to adaptive thermogenesis.''; PubMed Europe PMC Scholia
  39. Iwaki M, Matsuda M, Maeda N, Funahashi T, Matsuzawa Y, Makishima M, Shimomura I.; ''Induction of adiponectin, a fat-derived antidiabetic and antiatherogenic factor, by nuclear receptors.''; PubMed Europe PMC Scholia
  40. Yeh WC, Cao Z, Classon M, McKnight SL.; ''Cascade regulation of terminal adipocyte differentiation by three members of the C/EBP family of leucine zipper proteins.''; PubMed Europe PMC Scholia
  41. Gesta S, Tseng YH, Kahn CR.; ''Developmental origin of fat: tracking obesity to its source.''; PubMed Europe PMC Scholia
  42. Fischer-Posovszky P, Newell FS, Wabitsch M, Tornqvist HE.; ''Human SGBS cells - a unique tool for studies of human fat cell biology.''; PubMed Europe PMC Scholia
  43. Farmer SR.; ''Transcriptional control of adipocyte formation.''; PubMed Europe PMC Scholia
  44. Ni Y, Ji C, Wang B, Qiu J, Wang J, Guo X.; ''A Novel pro-adipogenesis factor abundant in adipose tissues and over-expressed in obesity acts upstream of PPARγ and C/EBPα.''; PubMed Europe PMC Scholia
  45. Cao Z, Umek RM, McKnight SL.; ''Regulated expression of three C/EBP isoforms during adipose conversion of 3T3-L1 cells.''; PubMed Europe PMC Scholia
  46. Morganstein DL, Wu P, Mane MR, Fisk NM, White R, Parker MG.; ''Human fetal mesenchymal stem cells differentiate into brown and white adipocytes: a role for ERRalpha in human UCP1 expression.''; PubMed Europe PMC Scholia

History

View all...
CompareRevisionActionTimeUserComment
116666view12:48, 9 May 2021EweitzOntology Term : 'white fat cell' added !
114880view16:39, 25 January 2021ReactomeTeamReactome version 75
113326view11:39, 2 November 2020ReactomeTeamReactome version 74
112537view15:50, 9 October 2020ReactomeTeamReactome version 73
101450view11:32, 1 November 2018ReactomeTeamreactome version 66
100988view21:10, 31 October 2018ReactomeTeamreactome version 65
100524view19:44, 31 October 2018ReactomeTeamreactome version 64
100071view16:28, 31 October 2018ReactomeTeamreactome version 63
99622view15:01, 31 October 2018ReactomeTeamreactome version 62 (2nd attempt)
99229view12:44, 31 October 2018ReactomeTeamreactome version 62
93818view13:38, 16 August 2017ReactomeTeamreactome version 61
93364view11:21, 9 August 2017ReactomeTeamreactome version 61
88360view16:39, 1 August 2016FehrhartOntology Term : 'regulatory pathway' added !
86448view09:18, 11 July 2016ReactomeTeamreactome version 56
83095view09:58, 18 November 2015ReactomeTeamVersion54
81767view10:12, 26 August 2015ReactomeTeamVersion53
76992view08:28, 17 July 2014ReactomeTeamFixed remaining interactions
76697view12:06, 16 July 2014ReactomeTeamFixed remaining interactions
76023view10:08, 11 June 2014ReactomeTeamRe-fixing comment source
75732view11:20, 10 June 2014ReactomeTeamReactome 48 Update
75082view14:03, 8 May 2014AnweshaFixing comment source for displaying WikiPathways description
74729view08:48, 30 April 2014ReactomeTeamNew pathway

External references

DataNodes

View all...
NameTypeDatabase referenceComment
13(S')-HODE [nucleoplasm]MetaboliteCHEBI:34154 (ChEBI)
4xPalmC-CD36ProteinP16671 (Uniprot-TrEMBL)
9S-HODE [nucleoplasm]MetaboliteCHEBI:34496 (ChEBI)
AA [nucleoplasm]MetaboliteCHEBI:15843 (ChEBI)
ADIPOQProteinQ15848 (Uniprot-TrEMBL)
ALA [nucleoplasm]MetaboliteCHEBI:27432 (ChEBI)
ANGPTL4ProteinQ9BY76 (Uniprot-TrEMBL)
Actos [nucleoplasm]MetaboliteCHEBI:8228 (ChEBI)
CARM1(2-608) [nucleoplasm]ProteinQ86X55 (Uniprot-TrEMBL)
CCNC [nucleoplasm]ProteinP24863 (Uniprot-TrEMBL)
CCND3ProteinP30281 (Uniprot-TrEMBL)
CDK19 [nucleoplasm]ProteinQ9BWU1 (Uniprot-TrEMBL)
CDK4(2-303)ProteinP11802 (Uniprot-TrEMBL)
CDK8 [nucleoplasm]ProteinP49336 (Uniprot-TrEMBL)
CEBPAProteinP49715 (Uniprot-TrEMBL)
CEBPBProteinP17676 (Uniprot-TrEMBL)
CEBPDProteinP49716 (Uniprot-TrEMBL)
CHD9 [nucleoplasm]ProteinQ3L8U1 (Uniprot-TrEMBL)
CREBBP(2-2442) [nucleoplasm]ProteinQ92793 (Uniprot-TrEMBL)
CREBBP(2-2442)ProteinQ92793 (Uniprot-TrEMBL)
EBF1ProteinQ9UH73 (Uniprot-TrEMBL)
EGR2ProteinP11161 (Uniprot-TrEMBL)
EP300(1-2414) [nucleoplasm]ProteinQ09472 (Uniprot-TrEMBL)
EP300(1-2414)ProteinQ09472 (Uniprot-TrEMBL)
EPA [nucleoplasm]MetaboliteCHEBI:28364 (ChEBI)
FABP4 [nucleoplasm]ProteinP15090 (Uniprot-TrEMBL)
FABP4:Ligands of PPARGComplexREACT_119193 (Reactome)
FABP4ProteinP15090 (Uniprot-TrEMBL)
GLUT4 tetramerComplexREACT_2699 (Reactome)
HDAC3 [nucleoplasm]ProteinO15379 (Uniprot-TrEMBL)
HDAC3ProteinO15379 (Uniprot-TrEMBL)
HELZ2 [nucleoplasm]ProteinQ9BYK8 (Uniprot-TrEMBL)
HELZ2ProteinQ9BYK8 (Uniprot-TrEMBL)
KLF4ProteinO43474 (Uniprot-TrEMBL)
KLF5ProteinQ13887 (Uniprot-TrEMBL)
LEPProteinP41159 (Uniprot-TrEMBL)
LINA [nucleoplasm]MetaboliteCHEBI:17351 (ChEBI)
LPLProteinP06858 (Uniprot-TrEMBL)
MED1 [nucleoplasm]ProteinQ15648 (Uniprot-TrEMBL) MED1 is a component of each of the various Mediator complexes, that function as transcription co-activators. The MED1-containing compolexes include the DRIP, ARC, TRIP and CRSP compllexes.
MED10(2-135) [nucleoplasm]ProteinQ9BTT4 (Uniprot-TrEMBL)
MED11 [nucleoplasm]ProteinQ9P086 (Uniprot-TrEMBL)
MED12 [nucleoplasm]ProteinQ93074 (Uniprot-TrEMBL)
MED13 [nucleoplasm]ProteinQ9UHV7 (Uniprot-TrEMBL)
MED13L [nucleoplasm]ProteinQ71F56 (Uniprot-TrEMBL)
MED14 [nucleoplasm]ProteinO60244 (Uniprot-TrEMBL)
MED15 [nucleoplasm]ProteinQ96RN5 (Uniprot-TrEMBL)
MED16 [nucleoplasm]ProteinQ9Y2X0 (Uniprot-TrEMBL)
MED17 [nucleoplasm]ProteinQ9NVC6 (Uniprot-TrEMBL)
MED18 [nucleoplasm]ProteinQ9BUE0 (Uniprot-TrEMBL)
MED19 [nucleoplasm]ProteinA0JLT2 (Uniprot-TrEMBL)
MED20 [nucleoplasm]ProteinQ9H944 (Uniprot-TrEMBL)
MED21 [nucleoplasm]ProteinQ13503 (Uniprot-TrEMBL)
MED22 [nucleoplasm]ProteinQ15528 (Uniprot-TrEMBL)
MED23 [nucleoplasm]ProteinQ9ULK4 (Uniprot-TrEMBL)
MED24 [nucleoplasm]ProteinO75448 (Uniprot-TrEMBL)
MED25 [nucleoplasm]ProteinQ71SY5 (Uniprot-TrEMBL)
MED26 [nucleoplasm]ProteinO95402 (Uniprot-TrEMBL)
MED27 [nucleoplasm]ProteinQ6P2C8 (Uniprot-TrEMBL)
MED29(2-200) [nucleoplasm]ProteinQ9NX70 (Uniprot-TrEMBL)
MED30(1-178) [nucleoplasm]ProteinQ96HR3 (Uniprot-TrEMBL)
MED31 [nucleoplasm]ProteinQ9Y3C7 (Uniprot-TrEMBL)
MED4 [nucleoplasm]ProteinQ9NPJ6 (Uniprot-TrEMBL)
MED6 [nucleoplasm]ProteinO75586 (Uniprot-TrEMBL)
MED7 [nucleoplasm]ProteinO43513 (Uniprot-TrEMBL)
MED8 [nucleoplasm]ProteinQ96G25 (Uniprot-TrEMBL)
MED9 [nucleoplasm]ProteinQ9NWA0 (Uniprot-TrEMBL)
Mediator Complex (consensus)ComplexREACT_27330 (Reactome) The Mediator Complex bridges transcription factors and the basal RNA polymerase II complex. Multiple analyses of immunoprecipitated complexes from human cells (HeLa cells) detects 31 subunits. Other complexes with fewer subunits may also exist.
NCOA1 [nucleoplasm]ProteinQ15788 (Uniprot-TrEMBL)
NCOA1ProteinQ15788 (Uniprot-TrEMBL)
NCOA2 [nucleoplasm]ProteinQ15596 (Uniprot-TrEMBL)
NCOA2ProteinQ15596 (Uniprot-TrEMBL)
NCOA3 [nucleoplasm]ProteinQ9Y6Q9 (Uniprot-TrEMBL)
NCOA3ProteinQ9Y6Q9 (Uniprot-TrEMBL)
NCOA6 [nucleoplasm]ProteinQ14686 (Uniprot-TrEMBL)
NCOR1 [nucleoplasm]ProteinO75376 (Uniprot-TrEMBL)
NCOR1ProteinO75376 (Uniprot-TrEMBL)
NCOR2 [nucleoplasm]ProteinQ9Y618 (Uniprot-TrEMBL)
NCOR2ProteinQ9Y618 (Uniprot-TrEMBL)
NF-kB complexComplexREACT_12775 (Reactome)
NFKB1(1-433) [nucleoplasm]ProteinP19838 (Uniprot-TrEMBL)
NR2F2ProteinP24468 (Uniprot-TrEMBL)
PCK1ProteinP35558 (Uniprot-TrEMBL)
PLIN1ProteinO60240 (Uniprot-TrEMBL)
PPARA [nucleoplasm]ProteinQ07869 (Uniprot-TrEMBL)
PPARA:RXRA Coactivator ComplexComplexREACT_20439 (Reactome)
PPARG [nucleoplasm]ProteinP37231 (Uniprot-TrEMBL)
PPARG:Fatty

Acid:RXRA:Mediator:Coactivator

Complex		ComplexREACT_27768 (Reactome)
PPARG:RXRA HeterodimerComplexREACT_27328 (Reactome)
PPARG:RXRA:Corepressor ComplexComplexREACT_27552 (Reactome)
PPARGC1A [nucleoplasm]ProteinQ9UBK2 (Uniprot-TrEMBL)
PPARGC1AProteinQ9UBK2 (Uniprot-TrEMBL)
PPARGProteinP37231 (Uniprot-TrEMBL)
Palm [nucleoplasm]MetaboliteCHEBI:15756 (ChEBI)
RELA [nucleoplasm]ProteinQ04206 (Uniprot-TrEMBL)
RGZ [nucleoplasm]MetaboliteCHEBI:50122 (ChEBI)
RXRA [nucleoplasm]ProteinP19793 (Uniprot-TrEMBL)
RXRAProteinP19793 (Uniprot-TrEMBL)
SLC2A4 [plasma membrane]ProteinP14672 (Uniprot-TrEMBL)
SMARCD3 [nucleoplasm]ProteinQ6STE5 (Uniprot-TrEMBL)
SREBF1A,2REACT_116516 (Reactome)
TBL1X [nucleoplasm]ProteinO60907 (Uniprot-TrEMBL)
TBL1XR1 [nucleoplasm]ProteinQ9BZK7 (Uniprot-TrEMBL)
TGFB1(279-390)ProteinP01137 (Uniprot-TrEMBL)
TGS1 [nucleoplasm]ProteinQ96RS0 (Uniprot-TrEMBL)
TNF(77-233)ProteinP01375 (Uniprot-TrEMBL)
WNT1,WNT10BProteinREACT_27326 (Reactome)

Annotated Interactions

View all...
SourceTargetTypeDatabase referenceComment
4xPalmC-CD36ArrowREACT_27168 (Reactome)
ADIPOQArrowREACT_27292 (Reactome)
ANGPTL4ArrowREACT_27173 (Reactome)
ArrowREACT_27244 (Reactome)
ArrowREACT_27292 (Reactome)
CCND3ArrowREACT_27226 (Reactome)
CDK4(2-303)ArrowREACT_27226 (Reactome)
CEBPAArrowREACT_27217 (Reactome)
CEBPAArrowREACT_27244 (Reactome)
CEBPAArrowREACT_27264 (Reactome)
CEBPAArrowREACT_27275 (Reactome)
CEBPAArrowREACT_27292 (Reactome)
CEBPBArrowREACT_27153 (Reactome)
CEBPBArrowREACT_27156 (Reactome)
CEBPBArrowREACT_27252 (Reactome)
CEBPBArrowREACT_27292 (Reactome)
CEBPBArrowREACT_27305 (Reactome)
CEBPDArrowREACT_27156 (Reactome)
CEBPDArrowREACT_27195 (Reactome)
CEBPDArrowREACT_27252 (Reactome)
CEBPDArrowREACT_27305 (Reactome)
CREBBP(2-2442)REACT_27257 (Reactome)
EBF1ArrowREACT_27156 (Reactome)
EBF1ArrowREACT_27252 (Reactome)
EGR2ArrowREACT_27153 (Reactome)
EP300(1-2414)REACT_27257 (Reactome)
FABP4:Ligands of PPARGREACT_27257 (Reactome)
FABP4ArrowREACT_27226 (Reactome)
FABP4ArrowREACT_27257 (Reactome)
GLUT4 tetramerArrowREACT_27264 (Reactome)
HDAC3ArrowREACT_27257 (Reactome)
HDAC3REACT_27280 (Reactome)
HELZ2REACT_27257 (Reactome)
KLF4ArrowREACT_27153 (Reactome)
KLF5ArrowREACT_27156 (Reactome)
KLF5ArrowREACT_27305 (Reactome)
LEPArrowREACT_27275 (Reactome)
LPLArrowREACT_27312 (Reactome)
Mediator Complex (consensus)REACT_27257 (Reactome)
NCOA1REACT_27257 (Reactome)
NCOA2REACT_27257 (Reactome)
NCOA3REACT_27257 (Reactome)
NCOR1ArrowREACT_27257 (Reactome)
NCOR1REACT_27280 (Reactome)
NCOR2ArrowREACT_27257 (Reactome)
NCOR2REACT_27280 (Reactome)
PCK1ArrowREACT_27194 (Reactome)
PLIN1ArrowREACT_27159 (Reactome)
PPARA:RXRA Coactivator ComplexArrowREACT_27168 (Reactome)
PPARA:RXRA Coactivator ComplexArrowREACT_27173 (Reactome)
PPARG:Fatty

Acid:RXRA:Mediator:Coactivator

Complex		ArrowREACT_27159 (Reactome)
PPARG:Fatty

Acid:RXRA:Mediator:Coactivator

Complex		ArrowREACT_27168 (Reactome)
PPARG:Fatty

Acid:RXRA:Mediator:Coactivator

Complex		ArrowREACT_27173 (Reactome)
PPARG:Fatty

Acid:RXRA:Mediator:Coactivator

Complex		ArrowREACT_27194 (Reactome)
PPARG:Fatty

Acid:RXRA:Mediator:Coactivator

Complex		ArrowREACT_27226 (Reactome)
PPARG:Fatty

Acid:RXRA:Mediator:Coactivator

Complex		ArrowREACT_27244 (Reactome)
PPARG:Fatty

Acid:RXRA:Mediator:Coactivator

Complex		ArrowREACT_27257 (Reactome)
PPARG:Fatty

Acid:RXRA:Mediator:Coactivator

Complex		ArrowREACT_27312 (Reactome)
PPARG:Fatty

Acid:RXRA:Mediator:Coactivator

Complex		TBarREACT_27275 (Reactome)
PPARG:RXRA HeterodimerArrowREACT_27277 (Reactome)
PPARG:RXRA HeterodimerREACT_27280 (Reactome)
PPARG:RXRA:Corepressor ComplexArrowREACT_27280 (Reactome)
PPARG:RXRA:Corepressor ComplexREACT_27257 (Reactome)
PPARG:RXRA:Corepressor ComplexTBarREACT_27264 (Reactome)
PPARGArrowREACT_27156 (Reactome)
PPARGArrowREACT_27217 (Reactome)
PPARGC1AREACT_27257 (Reactome)
PPARGREACT_27277 (Reactome)
REACT_27153 (Reactome) Expression of the CEBPB and CEBPD transcription factors is induced by at least three factors:
1) Mitogens such as those present in fetal serum act via the Krox20 transcription factor to activate expression of CEBPB.
2) Glucocorticoids activate expression of CEBPD.
3) Hormones or drugs that increase intracellular cAMP act via pCREB to activate expression of CEBPB.
The detailed mechanisms of activation are not yet known.
REACT_27156 (Reactome) The transcription factors CEBPB, CEBPD, and KLF5 simultaneously bind the PPARG promoter and synergistically activate transcription of the PPARG gene. These three factors activate transcription after initial stimulation of adipocyte differentiation but then are replaced by CEBPA within 10 days. CEBPA and other factors may be responsible for long term maintenance of PPARG expression and the differentiated state.
Pre-adipose tissue contains both the widely expressed PPARG isoform 1 mRNA and the more tissue-specific PPARG isoform 2. The PPARG isoform 2 mRNA is translated to yield PPARG isoform 2 protein, which has 505 amino acid residues (57 KDa) and is the longest of the 4 observed variants. Isoform 2 is specific to preadipose and adipose tissue (Mukherjee et al. 1997). Confusingly, the longest variant is called isoform 1 in some publications.
REACT_27159 (Reactome) The Perilipin (PLIN) gene is transcribed to yield mRNA and the mRNA is translated to yield protein. Expression of Perilipin is upregulated during adipogenesis.
REACT_27168 (Reactome) The Platelet glycoprotein IV gene (CD36, PAS IV, GPIV) is transcribed to yield mRNA and the mRNA is translated to yield proteind.
REACT_27173 (Reactome) The ANGPTL4 gene is transcribed to yield mRNA and the mRNA is translated to yield protein.
REACT_27194 (Reactome) The PEPCK-C gene is transcribed to yield mRNA and the mRNA is translated to yield protein.
REACT_27195 (Reactome) Expression of the CEBPB and CEBPD transcription factors is induced by at least three factors:
1) Mitogens such as those present in fetal serum act via the Krox20 transcription factor to activate expression of CEBPB.
2) Glucocorticoids activate expression of CEBPD.
3) Hormones or drugs that increase intracellular cAMP act via pCREB to activate expression of CEBPB.
The detailed mechanisms of activation are not yet known.
REACT_27217 (Reactome) In mouse, by 10 days after induction of adipocyte differentiation Cebpa, but neither Cebpb nor Cebpd, is detectable at the Pparg promoter. While adipocyte differentiation can proceed without Cebpa, adipocytes differentiated from Cebpa-knockout cells are insulin insensitive due to a defect in GLUT4 vesicle trafficking.
REACT_27226 (Reactome) The FABP4 gene is transcribed to yield mRNA and the mRNA is translated to yield protein. Expression of FABP4 is activated during adipogenesis.
REACT_27244 (Reactome) The CEBPA gene is transcribed to yield mRNA and the mRNA is translated to yield protein.
REACT_27252 (Reactome) The gene encoding transcription factor EBF1 is transcribed to yield mRNA and the mRNA is translated to yield protein in pre-adipocytes and adipocytes. Transcription of EBF1 is enhanced by CEBPB and CEBPD, which bind the EBF1 promoter.
REACT_27257 (Reactome) PPARG can be activated in cell cultures by adding ligands such as polyunsaturated fatty acids and certain prostanoids (prostaglandins). Endogenous fatty acids are relatively poor activators. Which ligands are most responsible for PPARG activation in the body has not yet been established. Generally, oxidized fatty acids such as 9(S')-hydroxyoctadeca-10,12-dienoic acid (9(S')-HODE) and 13(S')-HODE are more effective activators than are endogenous fatty acids. The thiazolidinedione (TZD) class of antidiabetic drugs are agonist ligands for PPARG (Lambe and Tugwood 1996).
FABP4 delivers ligands to PPARG directly. Binding of activator ligands to PPARG causes loss of corepressors such as SMRT/NCoR2, NCoR1, and HDAC3 and gain of interactions with the basal transcription machinery (Yoo et al. 2006). The TRAP220/MED1/DRIP205 subunit of the TRAP/Mediator (DRIP) complex binds directly to the LXXLL motif of PPARG and TRAP/Mediator is necessary for full transcriptional activation of target genes (Ge et al. 2008). PPARG also interacts with the MED14 subunit of the Mediator complex (Grontved et al. 2010).
Other coactivators, including NCOA1/SRC-1, NCOA2/TIF2/GRIP1, CBP, HAT/p300, and PRIP, interact with PPARG in a ligand-dependent way and enhance transcription (Gellman et al. 1999, Wallberg et al. 2003, Yang et al. 2000, Ge et al. 2002, Puigserver et al. 1999, Bugge et al. 2009, Steger et al. 2010).
The target genes of PPARG encode proteins involved in adipocyte differentiation (PGAR/ANGPTL4, PLIN, and aP2/FABP4), carbohydrate metabolism (PEPCK-C), and fatty acid transport (FAT/CD36, LPL).
REACT_27264 (Reactome) The GLUT4 gene is transcribed to yield mRNA and the mRNA is translated to yield protein.
REACT_27275 (Reactome) The Ob gene encoding leptin is transcribed to yield mRNA and translated to yield protein. Expression of leptin is positively regulated by C/EBPalpha (CEBPA, Miller et al. 1996, Melzner et al. 2002) and negatively regulated by PPARG in adipocytes (De Vos et al. 1996).
REACT_27277 (Reactome) PPARG binds the Retinoic acid X Receptor RXRA to form a heterodimer that has transcriptional acivation activity. The complex was initially called ARF6 when discovered. PPARG binds RXRA via the C-terminus and AF-2 regions of PPARG.
REACT_27280 (Reactome) The PPARG:RXRA heterodimer binds specific the PPRE element, two 6-bp DR-1 motifs separated by 1 nucleotide, in the promoters of target genes such as aP2/FABP4 even in the absence of fatty acid ligands that activate PPARG. When activating ligands of PPARG are absent PPARG:RXRA recruits corepressors such as NCoR2(SMRT), NCoR, and HDAC3 to maintain the target gene in an inactive state.
REACT_27292 (Reactome) The Adiponectin gene is transcribed to yield mRNA and the mRNA is translated to yield protein. Expression of Adiponectin is upregulated during adipogenesis by C/EBPalpha (CEBPA), PPARG, and CEBPB (Segawa et al. 2009, Qiao et al. 2005, Iwaki et al. 2003, Kita et al. 2005).
REACT_27305 (Reactome) Increased expression of KLF5 occurs after activation of the transcription factors CEBPB and CEBPD during differentiation and activation of KLF5 depends on CEBPB and CEBPD. Both CEBPB and CEBPD bind the promoter of the KLF5 gene upstream of the site of transcription initiation and activate transcription of KLF5.
REACT_27312 (Reactome) The LPL gene is transcribed to yield mRNA and the mRNA is translated to yield protein.
RXRAREACT_27277 (Reactome)
SREBF1A,2ArrowREACT_27156 (Reactome)
TBarREACT_27156 (Reactome)
TGFB1(279-390)TBarREACT_27156 (Reactome)
TGFB1(279-390)TBarREACT_27244 (Reactome)
TNF(77-233)TBarREACT_27244 (Reactome)
WNT1,WNT10BTBarREACT_27244 (Reactome)
Retrieved from "https://classic.wikipathways.org/index.php/Pathway:WP2751"
Personal tools