Nutrition, Metabolism & Genomics Group
Head: Prof. dr. Michael Müller

What is Nutrigenomics? Until recently, nutrition research concentrated on nutrient deficiencies and impairment of health. The advent of genomics -interpreted broadly as a suite of high-throughput technologies for the generation, processing, and application of scientific information about the composition and functions of genomes- has created unprecedented opportunities for increasing our understanding of how nutrients modulate gene and protein expression and ultimately influence cellular and organismal metabolism. Nutrigenomics can be seen as the combination of molecular nutrition and genomics. The diverse tissue and organ-specific effects of bioactive dietary components include gene expression patterns (transcriptome), organization of the chromatin (epigenome), protein expression patterns including post-translational modifications (proteome) as well as metabolite profiles (metabolome). Nutrigenomics will promote an increased understanding of how nutrition influences metabolic pathways and homeostatic control, how this regulation is disturbed in the early phases of diet-related disease, and the extent to which individual sensitizing genotypes contribute to such diseases. Eventually, nutrigenomics will lead to evidence-based dietary intervention strategies for restoring health and fitness and for preventing diet-related disease. (read for more Nature Reviews Genetics 4, 315-322 (2003)) (pdf) (recent review)

Eten volgens je genenpakket (Voeding Nu april 2008)
Je bent wat je eet, dat weten zelfs je genen (Volkskrant 21-6-2008)

 

The Nutrigenomics group studies the effects of nutrients on gene expression and metabolic pathways with the focus on:
1. Molecular pathways involved in nutrient-dependent changes in gene expression in liver, small intestine, adipose tissue, PBMCs and heart;
2. Impact of specific genes (e.g. ANGPTL4) and their products for energy metabolism;
3. Gene expression signatures of health and stress (the "two hits")

PhD position open:
Elucidation of molecular mechanisms involved in gut-fermentation induced satiety

Recent papers (more):
Angptl4 upregulates cholesterol synthesis in liver via inhibition of LPL- and HL-dependent hepatic cholesterol uptake (ATVB)
Fasting induces changes in PBMC gene expression profiles related to increases in fatty acid beta-oxidation (AJCN)

Effect of Synthetic Dietary Triglycerides: a Novel Research Paradigm for Nutrigenomics (Plos ONE)
Activation of PPARalpha in human PBMCs reveals an individual gene expression profile response (BMC Genomics)
PPARgamma activation promotes infiltration of alternatively activated macrophages into adipose tissue (JBC)

Nutrigenomics,
Molecular Nutrition
&
Genomics
We are members of
Nutrigenomics Consortium

NUGO (EC Network)
Netherlands  Genomics Initiative
Nutrigenomics Centres
NURSA
NUREBASE
PPARresource

NR Research Portal

Diabetes Genome Anatomy Project
Mouse Metabolic Phenotyping Centers
RACE
EDGE2
Lipidbank

GOLD (Lipidomics)
PharmGKB

Students:
Nutrigenomics & SysBiol Course

Nuclear Receptor signaling
Genetic science learning center
Lipids Online
Lipidmaps

References,
Text Mining &
more Genomics Links
DNA werd 50 jaar geleden ontdekt Over Genen en Genieten
Inaugural lecture 2002 (pdf)
Publications

Faculty of 1000 (Contributor)
 

PubMedline
Online Journals
Agralin Desktop library
GOOGLE Scholar "Nutrigenomics"
Medminer / PubCrawler
Scirus / GOOGLE Scholar
BioMed Central/ e-biosci
Nature Genomics
Functional Genomics
Functional Genomics
123Genomics
Bioinformatica pagina
euGenes: Human Genes
GenomesOnLineDatabases
Others Ingenuity 
Affymetrix
MADMAX
CLUSTALW
Expasy
BLAST
SOURCE
Stanford
Genomic Resources
Microarray Database
Eisen LAB
TopLinks
Travel by Train (NS)
Travel by Plane (KLM)
Voedingsacademie

Address:   
 

Prof. dr. Michael Müller
Nutrition, Metabolism and Genomics group
Division of Human Nutrition
Wageningen University
PO Box 8129
6700 EV Wageningen/ The Netherlands
Phone +31-317-482590
Fax     +31-317-483342
michael.muller@wur.nl