Functional coupling analysis suggests link between the obesity gene FTO and the BDNF-NTRK2 signaling pathway

Mathias Rask-Andersen, Markus S. Almén, Hans R. Olausen, Pawel K. Olszewski, Jenny Eriksson, Rohit A. Chavan, Allen S Levine, Robert Fredriksson, Helgi B. Schiöth

Research output: Contribution to journalArticlepeer-review

13 Scopus citations


Background: 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.Results: 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.Conclusions: 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).

Original languageEnglish (US)
Article number117
JournalBMC neuroscience
StatePublished - Nov 16 2011

Bibliographical note

Funding Information:
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.


Dive into the research topics of 'Functional coupling analysis suggests link between the obesity gene FTO and the BDNF-NTRK2 signaling pathway'. Together they form a unique fingerprint.

Cite this