TY - JOUR
T1 - Mapping ecologically relevant social behaviours by gene knockout in wild mice
AU - Halfin, L.
AU - Dayan, Molly
AU - Kimchi, Tali
AU - Chalfin, Lea
AU - Levy, Dana Rubi
AU - Austad, Steven N.
AU - Miller, Richard A.
AU - Iraqi, Fuad A.
AU - Dulac, Catherine
N1 - Funding Information: We thank T. Hajbi, S. Ovadia and S. Sullivan for the wild mouse maintenance support; B. Markus and E. Feldmesser for assistance with the genetic analysis; I. Koch and A. Chen for their comments on the manuscript. This work was supported by the Marie Curie Action International Integration Grant #249148 (T.K.), Peter and Patricia Gruber Research Award, the Women’s Health Research Center of the Weizmann Institute of Science (T.K.), the Joan and Jonathan Birnbach Family Laboratory Fund (T.K.), the Howard Hughes Medical Institute (C.D.) and the National Institutes of Health (C.D., T.K.).
PY - 2014/8/5
Y1 - 2014/8/5
N2 - The laboratory mouse serves as an important model system for studying gene, brain and behavioural interactions. Powerful methods of gene targeting have helped to decipher gene-function associations in human diseases. Yet, the laboratory mouse, obtained after decades of human-driven artificial selection, inbreeding, and adaptation to captivity, is of limited use for the study of fitness-driven behavioural responses that characterize the ancestral wild house mouse. Here, we demonstrate that the backcrossing of wild mice with knockout mutant laboratory mice retrieves behavioural traits exhibited exclusively by the wild house mouse, thereby unmasking gene functions inaccessible in the domesticated mutant model. Furthermore, we show that domestication had a much greater impact on females than on males, erasing many behavioural traits of the ancestral wild female. Hence, compared with laboratory mice, wild-derived mutant mice constitute an improved model system to gain insights into neuronal mechanisms underlying normal and pathological sexually dimorphic social behaviours.
AB - The laboratory mouse serves as an important model system for studying gene, brain and behavioural interactions. Powerful methods of gene targeting have helped to decipher gene-function associations in human diseases. Yet, the laboratory mouse, obtained after decades of human-driven artificial selection, inbreeding, and adaptation to captivity, is of limited use for the study of fitness-driven behavioural responses that characterize the ancestral wild house mouse. Here, we demonstrate that the backcrossing of wild mice with knockout mutant laboratory mice retrieves behavioural traits exhibited exclusively by the wild house mouse, thereby unmasking gene functions inaccessible in the domesticated mutant model. Furthermore, we show that domestication had a much greater impact on females than on males, erasing many behavioural traits of the ancestral wild female. Hence, compared with laboratory mice, wild-derived mutant mice constitute an improved model system to gain insights into neuronal mechanisms underlying normal and pathological sexually dimorphic social behaviours.
UR - http://www.scopus.com/inward/record.url?scp=84907374005&partnerID=8YFLogxK
U2 - https://doi.org/10.1038/ncomms5569
DO - https://doi.org/10.1038/ncomms5569
M3 - مقالة
SN - 2041-1723
VL - 5
JO - Nature Communications
JF - Nature Communications
M1 - 4569
ER -