Lopes-Cendes I, Scheffer I E, Berkovic S F, Rousseau M, Andermann E, Rouleau G A
Centre for Research in Neuroscience, The Montreal General Hospital Research Institute, Montreal Neurological Institute and Hospital, Montreal, Quebec, Canada.
Am J Hum Genet. 2000 Feb;66(2):698-701. doi: 10.1086/302768.
Generalized epilepsy with febrile seizures plus (GEFS+) is a recently recognized but relatively common form of inherited childhood-onset epilepsy with heterogeneous epilepsy phenotypes. We genotyped 41 family members, including 21 affected individuals, to localize the gene causing epilepsy in a large family segregating an autosomal dominant form of GEFS+. A genomewide search examining 197 markers identified linkage of GEFS+ to chromosome 2, on the basis of an initial positive LOD score for marker D2S294 (Z=4.4, recombination fraction [straight theta] = 0). A total of 24 markers were tested on chromosome 2q, to define the smallest candidate region for GEFS+. The highest two-point LOD score (Zmax=5.29; straight theta=0) was obtained with marker D2S324. Critical recombination events mapped the GEFS+ gene to a 29-cM region flanked by markers D2S156 and D2S311, with the idiopathic generalized epilepsy locus thereby assigned to chromosome 2q23-q31. The existence of the heterogeneous epilepsy phenotypes in this kindred suggests that seizure predisposition determined by the GEFS+ gene on chromosome 2q could be modified by other genes and/or by environmental factors, to produce the different seizure types observed.
伴有热性惊厥附加症的全身性癫痫(GEFS+)是一种最近才被认识但相对常见的遗传性儿童期癫痫,具有异质性癫痫表型。我们对41名家庭成员进行了基因分型,其中包括21名受影响个体,以在一个分离常染色体显性形式GEFS+的大家庭中定位导致癫痫的基因。一项全基因组搜索检查了197个标记,基于标记D2S294的初始阳性LOD评分(Z = 4.4,重组率[直θ]= 0),确定GEFS+与2号染色体连锁。在2号染色体长臂上共测试了24个标记,以确定GEFS+的最小候选区域。标记D2S324获得了最高的两点LOD评分(Zmax = 5.29;直θ = 0)。关键的重组事件将GEFS+基因定位到一个29厘摩的区域,该区域两侧是标记D2S156和D2S311,特发性全身性癫痫位点因此被定位到2号染色体长臂2区3带至3区1带。这个家系中异质性癫痫表型的存在表明,2号染色体长臂上由GEFS+基因决定的癫痫易感性可能会被其他基因和/或环境因素改变,从而产生所观察到的不同癫痫类型。