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Computational dissection of human episodic memory reveals mental process-specific genetic profiles

Date Issued
2015-01-01
Author(s)
Luksys, Gediminas  
Fastenrath, Matthias  
Coynel, David  
Freytag, Virginie  
Gschwind, Leo  
Heck, Angela  
Jessen, Frank
Maier, Wolfgang
Milnik, Annette  
Riedel-Heller, Steffi G.
Scherer, Martin
Spalek, Klara
Vogler, Christian  
Wagner, Michael
Wolfsgruber, Steffen
Papassotiropoulos, Andreas  
de Quervain, Dominique J.-F.  
DOI
10.1073/pnas.1500860112
Abstract
Episodic memory performance is the result of distinct mental processes, such as learning, memory maintenance, and emotional modulation of memory strength. Such processes can be effectively dissociated using computational models. Here we performed gene set enrichment analyses of model parameters estimated from the episodic memory performance of 1,765 healthy young adults. We report robust and replicated associations of the amine compound SLC (solute-carrier) transporters gene set with the learning rate, of the collagen formation and transmembrane receptor protein tyrosine kinase activity gene sets with the modulation of memory strength by negative emotional arousal, and of the L1 cell adhesion molecule (L1CAM) interactions gene set with the repetition-based memory improvement. Furthermore, in a large functional MRI sample of 795 subjects we found that the association between L1CAM interactions and memory maintenance revealed large clusters of differences in brain activity in frontal cortical areas. Our findings provide converging evidence that distinct genetic profiles underlie specific mental processes of human episodic memory. They also provide empirical support to previous theoretical and neurobiological studies linking specific neuromodulators to the learning rate and linking neural cell adhesion molecules to memory maintenance. Furthermore, our study suggests additional memory-related genetic pathways, which may contribute to a better understanding of the neurobiology of human memory.
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