Modular Genetic Control of Sexually Dimorphic Behaviors

被引:196
作者
Xu, Xiaohong [2 ]
Coats, Jennifer K. [1 ]
Yang, Cindy F. [1 ]
Wang, Amy [2 ]
Ahmed, Osama M. [1 ]
Alvarado, Maricruz [2 ]
Izumi, Tetsuro [3 ]
Shah, Nirao M. [1 ,2 ]
机构
[1] Univ Calif San Francisco, Program Neurosci, San Francisco, CA 94158 USA
[2] Univ Calif San Francisco, Dept Anat, San Francisco, CA 94158 USA
[3] Gunma Univ, Dept Mol Med, Maebashi, Gunma 3718512, Japan
关键词
ESTROGEN-RECEPTOR-ALPHA; VENTROMEDIAL HYPOTHALAMIC NUCLEUS; POSTERODORSAL MEDIAL AMYGDALA; NON-GENOMIC ACTIONS; MICE LACKING; MESSENGER-RNA; LORDOSIS BEHAVIOR; SEX-DIFFERENCES; RAT-BRAIN; TARGETED DISRUPTION;
D O I
10.1016/j.cell.2011.12.018
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Sex hormones such as estrogen and testosterone are essential for sexually dimorphic behaviors in vertebrates. However, the hormone-activated molecular mechanisms that control the development and function of the underlying neural circuits remain poorly defined. We have identified numerous sexually dimorphic gene expression patterns in the adult mouse hypothalamus and amygdala. We find that adult sex hormones regulate these expression patterns in a sex-specific, regionally restricted manner, suggesting that these genes regulate sex typical behaviors. Indeed, we find that mice with targeted disruptions of each of four of these genes (Brs3, Cckar, Irs4, Sytl4) exhibit extremely specific deficits in sex specific behaviors, with single genes controlling the pattern or extent of male sexual behavior, male aggression, maternal behavior, or female sexual behavior. Taken together, our findings demonstrate that various components of sexually dimorphic behaviors are governed by separable genetic programs.
引用
收藏
页码:596 / 607
页数:12
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