Enhanced partner preference in a promiscuous species by manipulating the expression of a single gene

被引:416
作者
Lim, MM
Wang, ZX
Olazábal, DE
Ren, XH
Terwilliger, EF
Young, LJ [1 ]
机构
[1] Emory Univ, Ctr Behav Neurosci, Atlanta, GA 30322 USA
[2] Emory Univ, Dept Psychiat & Behav Sci, Atlanta, GA 30322 USA
[3] Florida State Univ, Dept Psychol, Tallahassee, FL 32306 USA
[4] Florida State Univ, Program Neurosci, Tallahassee, FL 32306 USA
[5] Harvard Inst Med, Boston, MA 02115 USA
[6] Beth Israel Deaconess Med Ctr, Boston, MA 02215 USA
基金
美国国家科学基金会; 美国海洋和大气管理局; 美国国家卫生研究院;
关键词
D O I
10.1038/nature02539
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The molecular mechanisms underlying the evolution of complex behaviour are poorly understood. The mammalian genus Microtus provides an excellent model for investigating the evolution of social behaviour. Prairie voles (Microtus ochrogaster) exhibit a monogamous social structure in nature, whereas closely related meadow voles (Microtus pennsylvanicus) are solitary and polygamous(1). In male prairie voles, both vasopressin and dopamine act in the ventral forebrain to regulate selective affiliation between adult mates, known as pair bond formation, as assessed by partner preference in the laboratory(2-4). The vasopressin V1a receptor (V1aR) is expressed at higher levels in the ventral forebrain of monogamous than in promiscuous vole species(5), whereas dopamine receptor distribution is relatively conserved between species. Here we substantially increase partner preference formation in the socially promiscuous meadow vole by using viral vector V1aR gene transfer into the ventral forebrain. We show that a change in the expression of a single gene in the larger context of pre-existing genetic and neural circuits can profoundly alter social behaviour, providing a potential molecular mechanism for the rapid evolution of complex social behaviour.
引用
收藏
页码:754 / 757
页数:4
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