Literature DB >> 24979760

Dissociable contribution of prefrontal and striatal dopaminergic genes to learning in economic games.

Eric Set1, Ignacio Saez2, Lusha Zhu3, Daniel E Houser4, Noah Myung5, Songfa Zhong6, Richard P Ebstein7, Soo Hong Chew8, Ming Hsu9.   

Abstract

Game theory describes strategic interactions where success of players' actions depends on those of coplayers. In humans, substantial progress has been made at the neural level in characterizing the dopaminergic and frontostriatal mechanisms mediating such behavior. Here we combined computational modeling of strategic learning with a pathway approach to characterize association of strategic behavior with variations in the dopamine pathway. Specifically, using gene-set analysis, we systematically examined contribution of different dopamine genes to variation in a multistrategy competitive game captured by (i) the degree players anticipate and respond to actions of others (belief learning) and (ii) the speed with which such adaptations take place (learning rate). We found that variation in genes that primarily regulate prefrontal dopamine clearance--catechol-O-methyl transferase (COMT) and two isoforms of monoamine oxidase--modulated degree of belief learning across individuals. In contrast, we did not find significant association for other genes in the dopamine pathway. Furthermore, variation in genes that primarily regulate striatal dopamine function--dopamine transporter and D2 receptors--was significantly associated with the learning rate. We found that this was also the case with COMT, but not for other dopaminergic genes. Together, these findings highlight dissociable roles of frontostriatal systems in strategic learning and support the notion that genetic variation, organized along specific pathways, forms an important source of variation in complex phenotypes such as strategic behavior.

Entities:  

Keywords:  eigenSNPs; experience-weighted attraction; neuroeconomics

Mesh:

Substances:

Year:  2014        PMID: 24979760      PMCID: PMC4084431          DOI: 10.1073/pnas.1316259111

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


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