C57BL/6N Mutation in <i>Cytoplasmic FMRP interacting protein 2</i> Regulates Cocaine Response

Vivek Kumar, Kyungin Kim, Chryshanthi Joseph, Seung Hee Yoo, Hung Chung Huang, Martha Hotz Vitaterna, Fernando Pardo-Manuel de Villena, Gary A. Churchill, Antonello Bonci, Joseph S. Takahashi

Science · 2013 · 209 citations · 49 references

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Abstract

The inbred mouse C57BL/6J is the reference strain for genome sequence and for most behavioral and physiological phenotypes. However, the International Knockout Mouse Consortium uses an embryonic stem cell line derived from a related C57BL/6N substrain. We found that C57BL/6N has a lower acute and sensitized response to cocaine and methamphetamine. We mapped a single causative locus and identified a nonsynonymous mutation of serine to phenylalanine (S968F) in Cytoplasmic FMRP interacting protein 2 (Cyfip2) as the causative variant. The S968F mutation destabilizes CYFIP2, and deletion of the C57BL/6N mutant allele leads to acute and sensitized cocaine-response phenotypes. We propose that CYFIP2 is a key regulator of cocaine response in mammals and present a framework to use mouse substrains to identify previously unknown genes and alleles regulating behavior.

References

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