Neumann P E, Seyfried T N
Department of Neurology, Children's Hospital, Boston, Massachusetts 02115.
Behav Genet. 1990 Mar;20(2):307-23. doi: 10.1007/BF01067798.
The difference in susceptibility to audiogenic seizures (AGS) between C57BL/6J and DBA/2J inbred strains of mice is due to multiple genetic factors. AGS susceptibility was tested in 21-day-old mice from classical crosses, BXD recombinant inbred (RI) strains, a congenic DBA/2N.B6N-Ahb inbred strain and crosses between the BXD RI strains and DBA/2J. Analysis of these data reveals that the variation in AGS susceptibility between these two strains results from allelic differences at three or more loci. Most of the variation is due to allelic differences at two loci. The first, Asp-1 (formerly Ias), is a major gene located on chromosome 12, between Ah and D12 Nyul. The second, Asp-2 (formerly asp), is a minor gene located on chromosome 4, tightly linked to b. The negative correlation of brain stem Ca2(+)-ATPase activity and AGS susceptibility in the BXD RI strains suggests that the strain difference in Ca2(+)-ATPase activity is inherited as a polygenic trait and that Asp-1 and Asp-2 are linked to, or identical to, factors that influence Ca2(+)-ATPase activity.
C57BL/6J和DBA/2J近交系小鼠对听源性癫痫(AGS)易感性的差异是由多种遗传因素造成的。对来自经典杂交、BXD重组近交(RI)系、同基因DBA/2N.B6N-Ahb近交系的21日龄小鼠以及BXD RI系与DBA/2J之间的杂交后代进行了AGS易感性测试。对这些数据的分析表明,这两个品系之间AGS易感性的差异是由三个或更多位点的等位基因差异导致的。大部分差异是由两个位点的等位基因差异引起的。第一个位点是Asp-1(以前称为Ias),是位于12号染色体上Ah和D12 Nyul之间的一个主要基因。第二个位点是Asp-2(以前称为asp),是位于4号染色体上与b紧密连锁的一个次要基因。BXD RI系中脑干Ca2(+)-ATP酶活性与AGS易感性的负相关表明,Ca2(+)-ATP酶活性的品系差异作为一种多基因性状遗传,并且Asp-1和Asp-2与影响Ca2(+)-ATP酶活性的因子连锁或相同。