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Genetic mapping in Collaborative Cross mouse strains identifies loci that affect initial sensitivity to cocaine

Schoenrock, S. A.; Gaines, C. H.; Kumar, P.; Khan, S. A.; Farrington, J.; Ferris, M. T.; Pardo-Manuel de Villena, F.; Valdar, W.; Bubier, J.; Tarantino, L. M.

2025-01-12 genetics
10.1101/2025.01.12.629464 bioRxiv
Show abstract

We identified two Collaborative Cross (CC) strains, CC004/TauUncJ (CC004) and CC041/TauUncJ (CC041), that differ significantly for locomotor response and self-administration of cocaine. In the current study, we crossed each of these strains to C57BL/6NJ (B6N) mice to produce two F2 populations and identify genetic loci that influence locomotor response to cocaine. We identified three significant loci on chromosomes 7, 11 and 14 in the CC041 F2 mapping cross that collectively explain 14% of the phenotypic variance for locomotor response to cocaine. We used a bioinformatic approach to identify high quality candidate genes that are genetically plausible, have functional relevance and are suitable for further exploration. Our study is the first to use CC strains to perform QTL mapping for addiction-related phenotypes and proposes several candidate genes for follow-up analyses.

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