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癫痫性EL小鼠中由多个基因决定的一个主要效应数量性状基因座。

A major effect QTL determined by multiple genes in epileptic EL mice.

作者信息

Legare M E, Bartlett F S, Frankel W N

机构信息

The Jackson Laboratory, Bar Harbor, Maine 04609 USA.

出版信息

Genome Res. 2000 Jan;10(1):42-8.

Abstract

The EL mouse strain provides a polygenic model for epilepsy. Previous mapping experiments between EL and nonepileptic ABP mice identified, and a congenic strain confirmed, a quantitative trait locus (QTL), El2, which lowered the threshold to seizures induced by gentle rhythmic tossing. To narrow the map interval further we used a nested strategy to analyze a series of recombinants derived from the congenic strain. The recombinant strains revealed a complex pattern of inheritance, with at least two independent regions of Chromosome 2 necessary for rhythmic tossing seizures and additional regions associated with unusual gender effects. Similar results obtained using a completely independent paradigm, pentylenetetrazole-induced tonic-clonic seizures, exclude the possibility that the genetic complexity was a unique property of the testing assay. Thus, although conventional QTL mapping efforts detected and appeared to confirm a trait locus with effects large enough for fine-structure mapping, subsequent dissection revealed multiple loci. Although at least one of these loci was mapped to a 1-cM interval, its individual effect is small, perhaps approaching the practical limits for further study. Our results in the EL mouse may be prophetic for similar assaults on other polygenic, composite neurological behaviors which vary among inbred strains, begging the consideration of alternative strategies toward gene identification in these models.

摘要

EL小鼠品系为癫痫提供了一个多基因模型。先前在EL小鼠和非癫痫性ABP小鼠之间进行的定位实验确定了一个数量性状基因座(QTL)El2,一个同源近交系证实了该基因座,它降低了由轻柔有节奏摇晃诱导癫痫发作的阈值。为了进一步缩小定位区间,我们采用了嵌套策略来分析一系列源自该同源近交系的重组体。这些重组体显示出复杂的遗传模式,2号染色体上至少有两个独立区域是有节奏摇晃诱发癫痫发作所必需的,还有其他区域与异常的性别效应有关。使用完全独立的范式——戊四氮诱导的强直阵挛性癫痫发作——获得的类似结果排除了遗传复杂性是测试方法所特有的可能性。因此,尽管传统的QTL定位研究检测到并似乎证实了一个效应大到足以进行精细结构定位的性状基因座,但随后的剖析揭示了多个基因座。尽管这些基因座中至少有一个被定位到一个1厘摩的区间,但其个体效应很小,可能接近进一步研究的实际极限。我们在EL小鼠中的研究结果对于针对其他在近交系中存在差异的多基因复合神经行为的类似研究可能具有预示性,这促使我们考虑在这些模型中采用替代策略来进行基因鉴定。

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