Center for Neurobiology and Behavior, Department of Psychiatry, Translational Research Laboratory, University of Pennsylvania School of Medicine, Philadelphia, PA 19104-3403, USA.
Genes Brain Behav. 2011 Feb;10(1):57-68. doi: 10.1111/j.1601-183X.2010.00640.x. Epub 2010 Oct 5.
Aggressive behaviors are disabling, treatment refractory, and sometimes lethal symptoms of several neuropsychiatric disorders. However, currently available treatments for patients are inadequate, and the underlying genetics and neurobiology of aggression is only beginning to be elucidated. Inbred mouse strains are useful for identifying genomic regions, and ultimately the relevant gene variants (alleles) in these regions, that affect mammalian aggressive behaviors, which, in turn, may help to identify neurobiological pathways that mediate aggression. The BALB/cJ inbred mouse strain exhibits relatively high levels of intermale aggressive behaviors and shows multiple brain and behavioral phenotypes relevant to neuropsychiatric syndromes associated with aggression. The A/J strain shows very low levels of aggression. We hypothesized that a cross between BALB/cJ and A/J inbred strains would reveal genomic loci that influence the tendency to initiate intermale aggressive behavior. To identify such loci, we conducted a genomewide scan in an F2 population of 660 male mice bred from BALB/cJ and A/J inbred mouse strains. Three significant loci on chromosomes 5, 10 and 15 that influence aggression were identified. The chromosome 5 and 15 loci are completely novel, and the chromosome 10 locus overlaps an aggression locus mapped in our previous study that used NZB/B1NJ and A/J as progenitor strains. Haplotype analysis of BALB/cJ, NZB/B1NJ and A/J strains showed three positional candidate genes in the chromosome 10 locus. Future studies involving fine genetic mapping of these loci as well as additional candidate gene analysis may lead to an improved biological understanding of mammalian aggressive behaviors.
攻击行为是几种神经精神疾病的致残、治疗抵抗甚至有时致命的症状。然而,目前对患者的治疗方法还不够充分,攻击行为的潜在遗传学和神经生物学才刚刚开始被阐明。近交系小鼠品系可用于鉴定基因组区域,最终鉴定出这些区域影响哺乳动物攻击行为的相关基因变异(等位基因),这反过来可能有助于确定介导攻击行为的神经生物学途径。BALB/cJ 近交系小鼠表现出相对较高水平的雄性间攻击行为,并表现出与攻击相关的神经精神综合征相关的多种大脑和行为表型。A/J 品系的攻击性非常低。我们假设 BALB/cJ 和 A/J 近交系之间的杂交会揭示影响雄性间攻击行为倾向的基因组位点。为了鉴定这些位点,我们在 BALB/cJ 和 A/J 近交系繁殖的 660 只雄性 F2 群体中进行了全基因组扫描。鉴定出三个影响攻击行为的染色体 5、10 和 15 上的显著位点。染色体 5 和 15 位点是完全新的,染色体 10 位点与我们之前使用 NZB/B1NJ 和 A/J 作为亲本品系进行的研究中映射的攻击位点重叠。BALB/cJ、NZB/B1NJ 和 A/J 品系的单倍型分析显示,染色体 10 位点有三个候选基因。对这些位点进行精细遗传作图和其他候选基因分析的未来研究可能会提高对哺乳动物攻击行为的生物学理解。