Abstract
In analogy with the accepted view that behaviour is shaped by genexenvironment (GxE) interactions, GxE studies are exponentially increasing in the field of psychiatry. Whereas research was primarily driven by the premature view that negative environmental stimuli can trigger psychopathology in those subjects that are genetically predisposed, a closer look at the available data shows that GxE interactions are much more complex than initially thought. Here, we discuss GxE studies focussing on serotonin transporter (5-HTT, SERT, SLC6A4) gene variation in humans, monkeys, and rodents. Recent studies, across species, confirm the theorized 'for-better-and-for-worse' effect of low activity serotonin transporter genotypes. In addition, while 5-HTTxE interactions were thought to take place in early life, recent evidence illustrates that these interactions are also manifested in adulthood. Therefore, we discuss data based on 5-HTTxE interactions, and propose a model in which predictive adaptive responses (PARs), as shaped by early life 5-HTTxE interactions, shape responses to environmental challenges in later life, i.e. reflecting 5-HTTxExE interactions.
