Lee, A.W.* ; Hengstler, H.* ; Schwald, K.* ; Berriel Diaz, M.* ; Loreth, D.* ; Kirsch, M.* ; Kretz, O.* ; Haas, C.A.* ; Hrabě de Angelis, M. ; Herzig, S.* ; Brümmendorf, T.* ; Klingenspor, M.* ; Rathjen, F.G.* ; Rozman, J. ; Nicholson, G.* ; Cox, R.D.* ; Schäfer, M.K.*
     
 
    
        
Functional inactivation of the genome-wide association study obesity gene neuronal growth regulator 1 in mice causes a body mass phenotype.
    
    
        
    
    
        
        PLoS ONE 7:e41537 (2012)
    
    
    
		
		
			
				To date, genome-wide association studies (GWAS) have identified at least 32 novel loci for obesity and body mass-related traits. However, the causal genetic variant and molecular mechanisms of specific susceptibility genes in relation to obesity are yet to be fully confirmed and characterised. Here, we examined whether the candidate gene NEGR1 encoding the neuronal growth regulator 1, also termed neurotractin or Kilon, accounts for the obesity association. To characterise the function of NEGR1 for body weight control in vivo, we generated two novel mutant mouse lines, including a constitutive NEGR1-deficient mouse line as well as an ENU-mutagenised line carrying a loss-of-function mutation (Negr1-I87N) and performed metabolic phenotypic analyses. Ablation of NEGR1 results in a small but steady reduction of body mass in both mutant lines, accompanied with a small reduction in body length in the Negr1-I87N mutants. Magnetic resonance scanning reveals that the reduction of body mass in Negr1-I87N mice is due to a reduced proportion of lean mass. Negr1-I87N mutants display reduced food intake and physical activity while normalised energy expenditure remains unchanged. Expression analyses confirmed the brain-specific distribution of NEGR1 including strong expression in the hypothalamus. In vitro assays show that NEGR1 promotes cell-cell adhesion and neurite growth of hypothalamic neurons. Our results indicate a role of NEGR1 in the control of body weight and food intake. This study provides evidence that supports the link of the GWAS candidate gene NEGR1 with body weight control.
			
			
				
			
		 
		
			
				
					
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        Publikationstyp
        Artikel: Journalartikel
    
 
    
        Dokumenttyp
        Wissenschaftlicher Artikel
    
 
    
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        Schlagwörter
        Obesity; NEGR1; GWAS; body weight control; CELL-ADHESION MOLECULE; INCREASED ENERGY-EXPENDITURE; EPITHELIAL OVARIAN-CANCER; NEURITE OUTGROWTH; IGLON FAMILY; HETEROPHILIC INTERACTIONS; TUMOR-SUPPRESSOR; NERVOUS-SYSTEM; DEFICIENT MICE; RAT-BRAIN
    
 
    
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        englisch
    
 
    
        Veröffentlichungsjahr
        2012
    
 
    
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        HGF-Berichtsjahr
        2012
    
 
    
    
        ISSN (print) / ISBN
        1932-6203
    
 
    
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	    Band: 7,  
	    Heft: 7,  
	    Seiten: ,  
	    Artikelnummer: e41537 
	    Supplement: ,  
	
    
 
  
        
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            Verlag
            Public Library of Science (PLoS)
        
 
        
            Verlagsort
            Lawrence, Kan.
        
 
	
        
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        Peer reviewed
    
 
     
    
        POF Topic(s)
        30201 - Metabolic Health
90000 - German Center for Diabetes Research
    
 
    
        Forschungsfeld(er)
        Genetics and Epidemiology
    
 
    
        PSP-Element(e)
        G-500600-003
G-500600-001
G-501900-066
G-501900-063
    
 
    
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        Erfassungsdatum
        2012-08-21