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小鼠纹状体酪氨酸羟化酶活性的遗传决定因素

Genetic determination of striatal tyrosine hydroxylase activity in mice.

作者信息

Vadász C, Sziráki I, Murthy L R, Lajtha A

出版信息

Neurochem Res. 1986 Aug;11(8):1139-49. doi: 10.1007/BF00965943.

Abstract

An additive major gene effect is described for tyrosine hydroxylase activity in mouse corpus striatum (CS). Quantitative genetic analysis indicated the presence of a segregating Mendelian factor with robust additive effect in F2 generations derived from crossing two highly inbred mouse strains, C57BL/6ByJ and BALB/cJ, with intermediate (INT) and high (HI) TH activity in CS. Significant positive correlation was found between striatal and mesencephalic TH activity in the segregating generations, raising the possibility that a common single gene may express its effect through pleiotropy or linkage. Genetic preparations taking advantage of the major gene effect should serve well as animal models of DA-mediated neuropsychiatric disorders.

摘要

在小鼠纹状体(CS)中描述了酪氨酸羟化酶活性的加性主基因效应。数量遗传学分析表明,在由两个高度近交的小鼠品系C57BL/6ByJ和BALB/cJ杂交产生的F2代中,存在一个具有强大加性效应的分离孟德尔因子,其CS中的酪氨酸羟化酶(TH)活性处于中等(INT)和高(HI)水平。在分离世代中,纹状体和中脑TH活性之间发现了显著的正相关,这增加了一种可能性,即一个共同的单基因可能通过多效性或连锁来表达其效应。利用主基因效应的遗传制剂应能很好地作为多巴胺介导的神经精神疾病的动物模型。

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