Vadász C, Sziráki I, Murthy L R, Vadász I, Badalamenti A F, Kóbor G, Lajtha A
Laboratory of Neurobehavioral Genetics, Nathan S. Kline Institute, Orangeburg, NY 10962.
J Neurogenet. 1987 Aug;4(5):241-52.
The hereditary factors that affect mesencephalic tyrosine hydroxylase (TH) activity were investigated in highly inbred mouse strains (CXBI/ByJ, C57BL/6ByJ, and BALB/cJ). The progenitor strains and their F1 hybrids, were compared for mesencephalic TH activity with each other and with replicated F2 generations. Quantitative and non-parametric genetic analysis of the data raise the possibility that there is a major gene with robust additive effect that is primarily responsible for the difference between the progenitor strains with intermediate and high mesencephalic TH activity. Strain differences in mesencephalic TH activity have been linked to differences in number of dopamine (DA) neurons in that area. If genetic variation of mesencephalic TH activity is entirely attributable to variation in number of mesencephalic dopamine (DA) neurons, identification of the genetic sources of variation of mesencephalic TH activity may take us a step closer to animal models and preparations that are needed in the study of the physiological and constitutional mechanisms of human disorders in which DA neurotransmission is involved.
在高度近交的小鼠品系(CXBI/ByJ、C57BL/6ByJ和BALB/cJ)中研究了影响中脑酪氨酸羟化酶(TH)活性的遗传因素。比较了亲本品系及其F1杂种之间以及与重复的F2代的中脑TH活性。对数据进行的定量和非参数遗传分析提出了一种可能性,即存在一个具有强大加性效应的主基因,该基因主要负责中脑TH活性中等和高的亲本品系之间的差异。中脑TH活性的品系差异与该区域多巴胺(DA)神经元数量的差异有关。如果中脑TH活性的遗传变异完全归因于中脑多巴胺(DA)神经元数量的变异,那么确定中脑TH活性变异的遗传来源可能会使我们更接近研究涉及DA神经传递的人类疾病的生理和体质机制所需的动物模型和制剂。