The brain-related phenotypes observed in 22q11.2 deletion syndrome (DS) patients are highly variable, and their origin is poorly understood. Changes in brain metabolism might contribute to these phenotypes, as many of the deleted genes are involved in metabolic processes, but this is unknown. This study shows for the first time thatTbx1haploinsufficiency causes brain metabolic imbalance. We studied two mouse models of 22q11.2DS using mass spectrometry, nuclear magnetic resonance spectroscopy, and transcriptomics. We found thatTbx1+/−mice andDf1/+mice, with a multigenic deletion that includesTbx1, have elevated brain methylmalonic acid, which is highly brain-toxic. Focusing onTbx1mutants, we found that they also have a more general brain metabolomic imbalance that affects key metabolic pathways, such as glutamine-glutamate and fatty acid metabolism. We provide transcriptomic evidence of a genotype-vitamin B12 treatment interaction. In addition, vitamin B12 treatment rescued a behavioural anomaly inTbx1+/−mice. Further studies will be required to establish whether the specific metabolites affected byTbx1haploinsufficiency are potential biomarkers of brain disease status in 22q11.2DS patients.
- Book : 8(2)
- Pub. Date : 2025
- Page : pp.e202403075
- Keyword :