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

Authors :
Yoo, S.-H.
Kourrich, S.
Kumar, V.
Huang, H. C.
Churchill, G.
Kim, K.
Joseph, C.
Bonci, A.
Takahashi, J. S.
Vitaterna, M. H.
Pardo-Manuel de Villena, F.
Publication Year :
2013
Publisher :
The University of North Carolina at Chapel Hill University Libraries, 2013.

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 lower acute and sensitized response to cocaine and methamphetamine. We mapped a single causative locus and identified a non-synonymous mutation of serine to phenylalanine (S968F) in Cytoplasmic FMR 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 CYFIP2 is a key regulator of cocaine response in mammals and present a framework to utilize mouse substrains to discover novel genes and alleles regulating behavior.

Details

Language :
English
Database :
OpenAIRE
Accession number :
edsair.doi...........0f40d2d0e70fec5505fbeff26fd8277f
Full Text :
https://doi.org/10.17615/rdkb-n146