Functional coupling analysis suggests link between the obesity gene FTO and the BDNF-NTRK2 signaling pathway
© Rask-Andersen et al; licensee BioMed Central Ltd. 2011
Received: 16 December 2010
Accepted: 16 November 2011
Published: 16 November 2011
The Fat mass and obesity gene (FTO) has been identified through genome wide association studies as an important genetic factor contributing to a higher body mass index (BMI). However, the molecular context in which this effect is mediated has yet to be determined. We investigated the potential molecular network for FTO by analyzing co-expression and protein-protein interaction databases, Coxpresdb and IntAct, as well as the functional coupling predicting multi-source database, FunCoup. Hypothalamic expression of FTO-linked genes defined with this bioinformatics approach was subsequently studied using quantitative real time-PCR in mouse feeding models known to affect FTO expression.
We identified several candidate genes for functional coupling to FTO through database studies and selected nine for further study in animal models. We observed hypothalamic expression of Profilin 2 (Pfn2), cAMP-dependent protein kinase catalytic subunit beta (Prkacb), Brain derived neurotrophic factor (Bdnf), neurotrophic tyrosine kinase, receptor, type 2 (Ntrk2), Signal transducer and activator of transcription 3 (Stat3), and Btbd12 to be co-regulated in concert with Fto. Pfn2 and Prkacb have previously not been linked to feeding regulation.
Gene expression studies validate several candidates generated through database studies of possible FTO-interactors. We speculate about a wider functional role for FTO in the context of current and recent findings, such as in extracellular ligand-induced neuronal plasticity via NTRK2/BDNF, possibly via interaction with the transcription factor CCAAT/enhancer binding protein β (C/EBPβ).
Genome-wide association studies consistently show that fat mass and obesity-related gene (FTO) gene polymorphism is the strongest known genetic factor associated with the development of higher BMI and obesity [1–5]. Several single nucleotide polymorphisms (SNPs) in this gene have been linked with elevated BMI in various populations [3, 6–12]. Recent studies have shown that FTO risk alleles are preferentially transcribed in heterozygote individuals, and this is facilitated by increased binding of transcription factor CUX1 to the regulatory elements in FTO intron 1 [13–15]. Transgenic mice carrying additional copies of the Fto gene also show an Fto expression-dependent body weight response .
Data obtained in studies on Fto knockout and mutant mice (FtoI367A) suggest that FTO is involved in energy homeostasis, metabolism and adipogenesis . Hypothalamic FTO is highly regulated in mouse and rat feeding models [18, 19]. However, our knowledge of the molecular and physiological functions of FTO is still very limited. The FTO protein has some structural similarities to canonical demethylase enzymes and its demethylating activity has been demonstrated in vitro. Recent data suggest a role for FTO in co-regulation of transcription. Using a reporter assay, Wu et al. were able to observe co-expression of FTO and CCAAT-enhancer binding protein β (C/EBPβ) to increase expression of a reporter gene driven by a C/EBP response element (CEBPRE). This element contained three CpG-sites for methylation and additional analysis showed coexpression of FTO and C/EBPβ to partially attenuate the reduced reporter gene expression induced by methylation of CEBPREs . C/EBPβ can be termed an "early-response" transcription factor, as it links extracellular signaling pathways to gene regulation and long-term changes in the cell's differentiation. It has been associated with a wide range of functions, from adipogenesis and energy homeostasis control to immune responses, neuroprotection, and synaptic plasticity [22, 23]. In line with that, dysregulation of FTO may lead not only to the impairment of energy homeostasis, but also to other abnormalities, including improper formation of neuronal networks. For example, a rare loss-of-function mutation documented in a Palestinian family showed that FTO deficiency leads to growth retardation and severe developmental defects of the central nervous system .
In order to determine a molecular mechanistic context for FTO, we utilized information from co-expression-, and protein-protein interaction databases and identified nine candidate genes for functional coupling to FTO. We then performed qRT-PCR expression analysis of murine hypothalami to detect whether the network candidate genes were co-regulated with FTO in a feeding restriction paradigm known to affect FTO expression in a differential manner. We found changes in the expression of Pfn2, Prkacb and Bdnf to parallel FTO mRNA upregulation during food deprivation. We also observed co-regulation of Fto and brain-derived neurotrophic factor (Bdnf) and its receptor TrkB (Ntrk2) in the sated state, and of Fto and Btbd12, Pfn2 and Stat3 in the food-deprived state.
Databases and gene interaction analysis
The FunCoup database (http://funcoup.sbc.su.se) predicts protein functional coupling through integration of data from a number of high-throughput functional assays. It uses information from 51 data sets containing mRNA and protein co-expression, protein-protein interaction, subcellular colocalization, phylogenetic profile similarity, shared transcription factor binding, shared miRNA targeting and domain associations. The database uses Bayesian statistics to predict the probability of functional coupling between two proteins and presents this as a probabilistic confidence value pfc) ranging from 0 to 1 . The Coxpresdb (coexpressed gene database) (http://coxpresdb.jp) uses Affymetrix GeneChip array data (Human Genome U133 plus 2.0 array and Mouse Genome 430 2.0 array) and presents interactions between genes based on probe-to-probe expression pattern similarities and estimates the strength of the interaction by combining the ranks of co-expression for the corresponding gene pair . The protein-protein interaction database IntAct (http://www.ebi.ac.uk/intact/main.xhtml) collects data from protein-protein interaction experiments, e.g. yeast two hybrid screenings and co-immunoprecipitation assays. The database allows submissions from independent research groups and currently encompasses data on approximately 200,000 protein-protein interactions in several species. IntAct also contains links to the publications describing the interactions . Databases were queried in default settings with "FTO" as the search term. Human FTO interactions were queried in Funcoup and results for the human FTO gene were selected in the Coxpresdb database.
Mouse feeding models
In the gene expression analysis, we utilized the tissue collected in the experiments described previously . In short, male C57BL/6J mice (Scanbur, Sweden) were housed individually or in groups of two in macrolon cages with LD 12:12 (lights on at 07.00). Animals were twelve weeks old at the beginning of the experiment. Water and standard chow (Lactamin, Sweden) were available ad libitum unless specified otherwise. All animal procedures were approved by the Uppsala Animal Ethical Committee (ID: C228/7 & C262/7) and followed the guidelines of Swedish legislation on animal experimentation (Animal Welfare Act SFS1998:56) and European Union legislation (Convention ETS123 and Directive 86/609/EEC).
16-hr food deprivation
Chow was removed just before the onset of darkness and mice were sacrificed 16 hours later. Control mice had ad libitum access to chow. Each group contained 8 animals. Hypothalami were dissected and immersed in RNAlater.
Ad libitum chow fed cohort
A larger group of ad libitum chow fed animals was used to better study co-regulation of FTO with other genes. 10 group-housed mice had ad libitum access to chow for 48 hours before sacrifice and dissection of hypothalami.
Generation of cDNA and qRT-PCR
The tissue was kept in RNAlater at room temperature for 2 h and then stored at -80°C until further processing. Tissues were homogenized by sonification (Branson sonifier B 15) and RNA was purified from the samples using the TRIzol (Sigma-Aldrich, Sweden) method . Samples were treated with Dnase I (Roche Diagnostics, Scandinavia) to remove residual DNA contamination. DNA contamination after Dnase I treatment was checked with PCR. Complementary DNA, cDNA, was then generated using reverse MLV reverse transcriptase (Invitrogen, Sweden) according to the manufacturer's specifications. PCR reactions were run in a total volume of 20 ul using Taq polymerase (Biotools, Sweden). Each reaction was performed in duplicate and contained 75 mM Tris/HCL, 50 mM KCl and 20 mM (NH4)2SO4, 4 mM MgCl2, 0.25 mM dNTPs, 1:20 DMSO, 20 mU/ul Taq polymerase, 50 mM forward and reverse primer and 1:4 SYBR-green (Invitrogen, Sweden). Reactions were run on iCycler temperature cyclers and fluorescence was measured using MyiQ single color real time PCR detection system. Data were analyzed using iQ5 software (BioRad, Sweden). Gene expression was normalized between the samples using the geometric mean of the most stable housekeeping genes, in accordance with the geNorm-method as previously published by Vandesompele et al. .
D'agostino & Pearson omnibus normality test was used to test normal distribution of gene expression data. Student's t-test was used to test the difference in gene expression between ad libitum chow fed, and food restricted mice. Linear regression was used to determine the relationship between expression of FTO and candidate genes. FTO was considered to correlate to candidate genes if the slope of the trendline significantly deviated from zero. For all tests nominal p-values < 0.05 were considered significant. The statistical analysis was performed with Prism v5.02 (GraphPad Software, San Diego, California, USA, http://www.graphpad.com).
Database analysis suggests several FTO-interaction candidates
Candidates genes for FTO-interaction studies based on results from queries in Funcoup, Coxpresdb and IntAct (see Figure 1).
Regulates actin polymerization in response to extracellular signals
Neurotrophic tyrosine kinase receptor type 2
Receptor for BDNF
Brain derived neurotrophic factor
involved in neuronal plasticity & differentiation
cAMP dependent protein kinase catalytic subunit beta
Ser/Thr protein kinase, catalytic subunit of AMP-activated protein kinase (AMPK)
Vesicle-associated membrane protein 2. alt. Synaptobrevin-2
Involved in the targeting and/or fusion of transport vesicles to their target membrane.
Signal transducer and activator of transcription 3
Transcription factor involved in cell growth and apoptosis. Responds to leptin signalling.
Hydrolyzes oligopeptides such as neurotensin, bradykinin and dynorphin A
SLX4 structure-specific endonuclease subunit homolog
DNA-repair, endonuclease activity.
Zinc finger and BTB domain-containing protein 20
May be a transcription factor that may be involved in hematopoiesis, oncogenesis, and immune responses
Activating transcription factor 7-interacting protein
A regulator of telomerase reverse transcriptase (TERT) expression
Feeding deprivation causes up-regulation of hypothalamic Fto, Pfn2 and Prkacb as well as down-regulation of Bdnf
Hypothalamic FTO is co-regulated with Ntrk2 and BDNF in chow fed mice
Correlation data for candidate genes.
95% Confidence Intervals
Goodness of Fit, R square
-0.1531 to 1.286
0.1165 to 0.9898
-0.7881 to -0.1488
-0.3902 to 0.2681
-2.319 to 2.905
-1.635 to 2.626
-1.469 to 2.737
-3.681 to 8.433
-1.129 to 5.710
0.2082 to 2.171
-0.54 to 0.73
-52 to 0.64
-1.198 to 1.113
-0.5620 to 1.983
0.01046 to 1.078
-0.4190 to 1.832
0.1775 to 3.198
-0.3582 to 1.664
We identified nine candidate genes for functional coupling and interaction to FTO through database analysis and previous publications. In order to test the validity of this network, expression of network candidate genes was analyzed in a food deprivation model known to induce up-regulation of Fto. We confirmed increased levels of Fto mRNA and observed simultaneous up-regulation of four out of the nine genes in the hypothalamus during food deprivation: Pfn2, Prkacb, TrkB and Stat3; as well as down-regulation of Bdnf. Bdnf, Ntrk2 and Stat3 have been previously implicated in the regulation of energy homeostasis. Bdnf inhibits feeding and increases energy expenditure when injected into the ventromedial hypothalamus (VMH) and paraventricular nucleus of the hypothalamus (PVN) [31–34]. Stat3 is required for the anorexic effect of leptin-receptor signalling in the ARH . Stat3 is also up-regulated in response to overexpression of AAV injection-induced Fto overexpression in the arcuate nucleus . However, two of the genes, Prkacb and Pfn2, have not previously been implicated in any feeding/obesity paradigms. Intriguingly, we observed the expression of Fto to correlate with expression of Ntrk2 and Bdnf in the hypothalamus of chow-fed mice (p = 0.019 and 0.011, respectively) (Figure 3 & Table 2). We also observed a strong linearity between Fto expression and that of Ntrk2 and Bdnf (R2 = 0.52 and 0.63, respectively) (Table 2).
The expression and co-regulation analysis provides additional evidence for a functional coupling of FTO to the network candidate genes and validates these databases in terms of co-expression [37, 38]. From this viewpoint, FunCoup has provided the most valuable leads as the genes it reports as candidates are shown not only to be regulated during starvation in a similar way as Fto, but also follows the expression of Fto in a linear fashion.
Based on our observations, we speculate that FTO may affect the regulation of ligand-induced neuronal plasticity via BDNF-NTRK2, PRKACB, STAT3 and PFN2. BDNF is involved in neuronal survivability, differentiation and formation of memory  and has also been associated to obesity in recent GWA-studies . Pfn2-encoded profyllin 2 regulates important cellular functions such as endocytosis, vesicle recycling and actin assembly in CNS neurons . Its effect on actin turnover may indicate a function in the regulation of neuronal plasticity in response to food intake. Neuronal plasticity occurs e.g. in the arcuate nucleus (ARH) in response to leptin signaling  and within the ARH - PVN pathways which develop during the perinatal period . Interestingly, some FTO polymorphisms are associated with lower brain volumes in the frontal and occipital lobes . As obesity itself is in some cases also associated with lower brain volume as well as cognitive deficits , FTO may be one of the genes bridging body weight dysregulation and other physiological abnormalities that oftentimes accompany abnormally low or high body weight. PRKACB (cAMP-dependant protein kinase catalytic subunit beta) encodes a catalytic subunit isoform of the protein kinase A holoenzyme (PKA). PRKACB phosphorylates the transcription factor, cAMP-response element-binding protein (CREB). CREB, in turn, regulates expression of several genes, including CEBPβ, BDNF, NTRK2, NPY and the glucocorticoid receptor. PRKACB has been linked to depression as lower expression of PRKACB in the prefrontal cortex occurs in major depression . STAT3 is a transcription factor involved in cell growth, embryogenesis, apoptosis and cell motility. It is also one of the mediators of leptin signaling and regulates the expression of appetite regulators Agouti related peptide (AGRP) and pro-opiomelanocortin (POMC) . This again suggests the potential role of Fto and its network of genes as a common molecular mechanism underlying co-regulation of body weight and processes related to cognition.
We identified several candidate genes for functional coupling to FTO through database analysis and validated these by expression studies in relevant feeding models via qRT-PCR. Based on these findings, we hypothesized about the molecular context of FTO, discussing a putative involvement in neuronal plasticity by association to transcription factors downstream of ligand activated signaling pathways such as BDNF/NTRK2. These functional results provide new ideas for deducing the mechanisms affected by obesity related FTO-risk alleles.
We thank Anica Klockars, Uppsala University for assistance with animal handling. The study was supported by the Swedish Research Council, Brain Research Foundation, Novo Nordisk, Tore Nilsons foundation and Åhlens foundation. R.F. was supported by the Göran Gustafsson foundation.
- Scuteri A, Sanna S, Chen WM, Uda M, Albai G, Strait J, Najjar S, Nagaraja R, Orru M, Usala G, et al.: Genome-wide association scan shows genetic variants in the FTO gene are associated with obesity-related traits. PLoS genetics. 2007, 3 (7): e115-10.1371/journal.pgen.0030115.PubMed CentralView ArticlePubMedGoogle Scholar
- Thorleifsson G, Walters GB, Gudbjartsson DF, Steinthorsdottir V, Sulem P, Helgadottir A, Styrkarsdottir U, Gretarsdottir S, Thorlacius S, Jonsdottir I, et al.: Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. Nature genetics. 2009, 41 (1): 18-24. 10.1038/ng.274.View ArticlePubMedGoogle Scholar
- Frayling TM, Timpson NJ, Weedon MN, Zeggini E, Freathy RM, Lindgren CM, Perry JR, Elliott KS, Lango H, Rayner NW, et al.: A common variant in the FTO gene is associated with body mass index and predisposes to childhood and adult obesity. Science (New York, NY). 2007, 316 (5826): 889-894. 10.1126/science.1141634.View ArticleGoogle Scholar
- Willer CJ, Speliotes EK, Loos RJ, Li S, Lindgren CM, Heid IM, Berndt SI, Elliott AL, Jackson AU, Lamina C, et al.: Six new loci associated with body mass index highlight a neuronal influence on body weight regulation. Nature genetics. 2009, 41 (1): 25-34. 10.1038/ng.287.PubMed CentralView ArticlePubMedGoogle Scholar
- Dina C, Meyre D, Gallina S, Durand E, Korner A, Jacobson P, Carlsson LM, Kiess W, Vatin V, Lecoeur C, et al.: Variation in FTO contributes to childhood obesity and severe adult obesity. Nature genetics. 2007, 39 (6): 724-726. 10.1038/ng2048.View ArticlePubMedGoogle Scholar
- Zhang G, Karns R, Narancic NS, Sun G, Cheng H, Missoni S, Durakovic Z, Rudan P, Chakraborty R, Deka R: Common SNPs in FTO gene are associated with obesity related anthropometric traits in an island population from the eastern Adriatic coast of Croatia. PLoS One. 2010, 5 (4): e10375-10.1371/journal.pone.0010375.PubMed CentralView ArticlePubMedGoogle Scholar
- Lee HJ, Kim IK, Kang JH, Ahn Y, Han BG, Lee JY, Song J: Effects of common FTO gene variants associated with BMI on dietary intake and physical activity in Koreans. Clin Chim Acta. 2010, 411 (21-22): 1716-1722. 10.1016/j.cca.2010.07.010.View ArticlePubMedGoogle Scholar
- Huang W, Sun Y, Sun J: Combined effects of FTO rs9939609 and MC4R rs17782313 on obesity and BMI in Chinese Han populations. Endocrine. 2010Google Scholar
- Hassanein MT, Lyon HN, Nguyen TT, Akylbekova EL, Waters K, Lettre G, Tayo B, Forrester T, Sarpong DF, Stram DO, et al.: Fine mapping of the association with obesity at the FTO locus in African-derived populations. Human molecular genetics. 2010, 19 (14): 2907-2916. 10.1093/hmg/ddq178.PubMed CentralView ArticlePubMedGoogle Scholar
- Adeyemo A, Chen G, Zhou J, Shriner D, Doumatey A, Huang H, Rotimi C: FTO genetic variation and association with obesity in West Africans and African Americans. Diabetes. 2010, 59 (6): 1549-1554. 10.2337/db09-1252.PubMed CentralView ArticlePubMedGoogle Scholar
- Bollepalli S, Dolan LM, Deka R, Martin LJ: Association of FTO gene variants with adiposity in African-American adolescents. Obesity (Silver Spring). 2010, 18 (10): 1959-1963. 10.1038/oby.2010.82.View ArticleGoogle Scholar
- Wangensteen T, Egeland T, Akselsen H, Holmen J, Undlien D, Retterstol L: FTO genotype and weight gain in obese and normal weight adults from a Norwegian population based cohort (the HUNT study). Exp Clin Endocrinol Diabetes. 2010, 118 (9): 649-652. 10.1055/s-0030-1249636.View ArticlePubMedGoogle Scholar
- Stratigopoulos G, Leduc CA, Cremona ML, Chung WK, Leibel RL: Cut-like homeobox 1 (CUX1) regulates expression of the fat mass and obesity-associated (FTO) and retinitis pigmentosa gtpase regulator interacting protein-1 like (RPGRIPIL) genes, and co-ordinates leptin receptor signaling. J Biol Chem. 2010Google Scholar
- Stratigopoulos G, Padilla SL, LeDuc CA, Watson E, Hattersley AT, McCarthy MI, Zeltser LM, Chung WK, Leibel RL: Regulation of Fto/Ftm gene expression in mice and humans. Am J Physiol Regul Integr Comp Physiol. 2008, 294 (4): R1185-1196. 10.1152/ajpregu.00839.2007.PubMed CentralView ArticlePubMedGoogle Scholar
- Berulava T, Horsthemke B: The obesity-associated SNPs in intron 1 of the FTO gene affect primary transcript levels. Eur J Hum Genet. 2010, 18 (9): 1054-1056. 10.1038/ejhg.2010.71.PubMed CentralView ArticlePubMedGoogle Scholar
- Church C, Moir L, McMurray F, Girard C, Banks GT, Teboul L, Wells S, Bruning JC, Nolan PM, Ashcroft FM, et al.: Overexpression of Fto leads to increased food intake and results in obesity. Nature genetics. 2010Google Scholar
- Church C, Lee S, Bagg EA, McTaggart JS, Deacon R, Gerken T, Lee A, Moir L, Mecinovic J, Quwailid MM, et al.: A mouse model for the metabolic effects of the human fat mass and obesity associated FTO gene. PLoS genetics. 2009, 5 (8): e1000599-10.1371/journal.pgen.1000599.PubMed CentralView ArticlePubMedGoogle Scholar
- Fredriksson R, Hagglund M, Olszewski PK, Stephansson O, Jacobsson JA, Olszewska AM, Levine AS, Lindblom J, Schioth HB: The obesity gene, FTO, is of ancient origin, up-regulated during food deprivation and expressed in neurons of feeding-related nuclei of the brain. Endocrinology. 2008, 149 (5): 2062-2071. 10.1210/en.2007-1457.View ArticlePubMedGoogle Scholar
- Olszewski PK, Fredriksson R, Olszewska AM, Stephansson O, Alsio J, Radomska KJ, Levine AS, Schioth HB: Hypothalamic FTO is associated with the regulation of energy intake not feeding reward. BMC neuroscience. 2009, 10: 129-10.1186/1471-2202-10-129.PubMed CentralView ArticlePubMedGoogle Scholar
- Gerken T, Girard CA, Tung YC, Webby CJ, Saudek V, Hewitson KS, Yeo GS, McDonough MA, Cunliffe S, McNeill LA, et al.: The obesity-associated FTO gene encodes a 2-oxoglutarate-dependent nucleic acid demethylase. Science (New York, NY). 2007, 318 (5855): 1469-1472. 10.1126/science.1151710.View ArticleGoogle Scholar
- Wu Q, Saunders RA, Szkudlarek-Mikho M, Serna ID, Chin KV: The obesity-associated Fto gene is a transcriptional coactivator. Biochemical and biophysical research communications.
- Nerlov C: Transcriptional and translational control of C/EBPs: the case for "deep" genetics to understand physiological function. Bioessays. 2010, 32 (8): 680-686. 10.1002/bies.201000004.View ArticlePubMedGoogle Scholar
- Nerlov C: The C/EBP family of transcription factors: a paradigm for interaction between gene expression and proliferation control. Trends Cell Biol. 2007, 17 (7): 318-324. 10.1016/j.tcb.2007.07.004.View ArticlePubMedGoogle Scholar
- Boissel S, Reish O, Proulx K, Kawagoe-Takaki H, Sedgwick B, Yeo GS, Meyre D, Golzio C, Molinari F, Kadhom N, et al.: Loss-of-function mutation in the dioxygenase-encoding FTO gene causes severe growth retardation and multiple malformations. American journal of human genetics. 2009, 85 (1): 106-111. 10.1016/j.ajhg.2009.06.002.PubMed CentralView ArticlePubMedGoogle Scholar
- Alexeyenko A, Sonnhammer EL: Global networks of functional coupling in eukaryotes from comprehensive data integration. Genome research. 2009, 19 (6): 1107-1116. 10.1101/gr.087528.108.PubMed CentralView ArticlePubMedGoogle Scholar
- Obayashi T, Hayashi S, Shibaoka M, Saeki M, Ohta H, Kinoshita K: COXPRESdb: a database of coexpressed gene networks in mammals. Nucleic acids research. 2008, D77-82. 36 Database
- Aranda B, Achuthan P, Alam-Faruque Y, Armean I, Bridge A, Derow C, Feuermann M, Ghanbarian AT, Kerrien S, Khadake J: The IntAct molecular interaction database in 2010. Nucleic acids research. D525-531. 38 Database
- Rio DC, Ares M, Hannon GJ, Nilsen TW: Purification of RNA using TRIzol (TRI reagent). Cold Spring Harbor protocols. 2010, pdb prot5439, 6Google Scholar
- Vandesompele J, De Preter K, Pattyn F, Poppe B, Van Roy N, De Paepe A, Speleman F: Accurate normalization of real-time quantitative RT-PCR data by geometric averaging of multiple internal control genes. Genome biology. 2002, 3 (7): RESEARCH0034.PubMed CentralView ArticlePubMedGoogle Scholar
- Svendsen JM, Smogorzewska A, Sowa ME, O'Connell BC, Gygi SP, Elledge SJ, Harper JW: Mammalian BTBD12/SLX4 assembles a Holliday junction resolvase and is required for DNA repair. Cell. 2009, 138 (1): 63-77. 10.1016/j.cell.2009.06.030.PubMed CentralView ArticlePubMedGoogle Scholar
- Wang C, Bomberg E, Billington C, Levine A, Kotz CM: Brain-derived neurotrophic factor in the hypothalamic paraventricular nucleus reduces energy intake. Am J Physiol Regul Integr Comp Physiol. 2007, 293 (3): R1003-1012. 10.1152/ajpregu.00011.2007.View ArticlePubMedGoogle Scholar
- Wang C, Bomberg E, Billington C, Levine A, Kotz CM: Brain-derived neurotrophic factor in the hypothalamic paraventricular nucleus increases energy expenditure by elevating metabolic rate. Am J Physiol Regul Integr Comp Physiol. 2007, 293 (3): R992-1002. 10.1152/ajpregu.00516.2006.View ArticlePubMedGoogle Scholar
- Wang C, Bomberg E, Billington CJ, Levine AS, Kotz CM: Brain-derived neurotrophic factor (BDNF) in the hypothalamic ventromedial nucleus increases energy expenditure. Brain Res. 2010, 1336: 66-77.PubMed CentralView ArticlePubMedGoogle Scholar
- Wang C, Bomberg E, Levine A, Billington C, Kotz CM: Brain-derived neurotrophic factor in the ventromedial nucleus of the hypothalamus reduces energy intake. Am J Physiol Regul Integr Comp Physiol. 2007, 293 (3): R1037-1045. 10.1152/ajpregu.00125.2007.View ArticlePubMedGoogle Scholar
- Myers MG, Cowley MA, Munzberg H: Mechanisms of leptin action and leptin resistance. Annu Rev Physiol. 2008, 70: 537-556. 10.1146/annurev.physiol.70.113006.100707.View ArticlePubMedGoogle Scholar
- Tung YC, Ayuso E, Shan X, Bosch F, O'Rahilly S, Coll AP, Yeo GS: Hypothalamic-specific manipulation of Fto, the ortholog of the human obesity gene FTO, affects food intake in rats. PLoS One. 2010, 5 (1): e8771-10.1371/journal.pone.0008771.PubMed CentralView ArticlePubMedGoogle Scholar
- Jansen R, Greenbaum D, Gerstein M: Relating whole-genome expression data with protein-protein interactions. Genome Res. 2002, 12 (1): 37-46. 10.1101/gr.205602.PubMed CentralView ArticlePubMedGoogle Scholar
- Jansen R, Yu H, Greenbaum D, Kluger Y, Krogan NJ, Chung S, Emili A, Snyder M, Greenblatt JF, Gerstein M: A Bayesian networks approach for predicting protein-protein interactions from genomic data. Science (New York, NY). 2003, 302 (5644): 449-453. 10.1126/science.1087361.View ArticleGoogle Scholar
- Calella AM, Nerlov C, Lopez RG, Sciarretta C, von Bohlen und Halbach O, Bereshchenko O, Minichiello L: Neurotrophin/Trk receptor signaling mediates C/EBPalpha, -beta and NeuroD recruitment to immediate-early gene promoters in neuronal cells and requires C/EBPs to induce immediate-early gene transcription. Neural development. 2007, 2: 4-10.1186/1749-8104-2-4.PubMed CentralView ArticlePubMedGoogle Scholar
- Bekinschtein P, Cammarota M, Izquierdo I, Medina JH: BDNF and memory formation and storage. Neuroscientist. 2008, 14 (2): 147-156.View ArticlePubMedGoogle Scholar
- Speliotes EK, Willer CJ, Berndt SI, Monda KL, Thorleifsson G, Jackson AU, Allen HL, Lindgren CM, Luan J, Magi R, et al.: Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index. Nat Genet. 2010, 42 (11): 937-948. 10.1038/ng.686.PubMed CentralView ArticlePubMedGoogle Scholar
- Lambrechts A, Braun A, Jonckheere V, Aszodi A, Lanier LM, Robbens J, Van Colen I, Vandekerckhove J, Fassler R, Ampe C: Profilin II is alternatively spliced, resulting in profilin isoforms that are differentially expressed and have distinct biochemical properties. Mol Cell Biol. 2000, 20 (21): 8209-8219. 10.1128/MCB.20.21.8209-8219.2000.PubMed CentralView ArticlePubMedGoogle Scholar
- Pinto S, Roseberry AG, Liu H, Diano S, Shanabrough M, Cai X, Friedman JM, Horvath TL: Rapid rewiring of arcuate nucleus feeding circuits by leptin. Science (New York, NY). 2004, 304 (5667): 110-115. 10.1126/science.1089459.View ArticleGoogle Scholar
- Bouret SG, Draper SJ, Simerly RB: Trophic action of leptin on hypothalamic neurons that regulate feeding. Science (New York, NY). 2004, 304 (5667): 108-110. 10.1126/science.1095004.View ArticleGoogle Scholar
- Ho AJ, Stein JL, Hua X, Lee S, Hibar DP, Leow AD, Dinov ID, Toga AW, Saykin AJ, Shen L, et al.: A commonly carried allele of the obesity-related FTO gene is associated with reduced brain volume in the healthy elderly. Proc Natl Acad Sci USA. 2010, 107 (18): 8404-8409. 10.1073/pnas.0910878107.PubMed CentralView ArticlePubMedGoogle Scholar
- Raji CA, Ho AJ, Parikshak NN, Becker JT, Lopez OL, Kuller LH, Hua X, Leow AD, Toga AW, Thompson PM: Brain structure and obesity. Hum Brain Mapp. 2010, 31 (3): 353-364.PubMed CentralPubMedGoogle Scholar
- Shelton RC, Hal Manier D, Lewis DA: Protein kinases A and C in post-mortem prefrontal cortex from persons with major depression and normal controls. Int J Neuropsychopharmacol. 2009, 12 (9): 1223-1232. 10.1017/S1461145709000285.View ArticlePubMedGoogle Scholar
- Bjorbaek C: Central leptin receptor action and resistance in obesity. J Investig Med. 2009, 57 (7): 789-794.PubMed CentralPubMedGoogle Scholar
- Zarubin T, Han J: Activation and signaling of the p38 MAP kinase pathway. Cell research. 2005, 15 (1): 11-18. 10.1038/sj.cr.7290257.View ArticlePubMedGoogle Scholar
- Yoshii A, Constantine-Paton M: Postsynaptic BDNF-TrkB signaling in synapse maturation, plasticity, and disease. Developmental neurobiology. 70 (5): 304-322.
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