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通过连锁分析将青少年型神经元蜡样脂褐质沉积症基因定位到16号染色体。

Mapping the gene for juvenile onset neuronal ceroid lipofuscinosis to chromosome 16 by linkage analysis.

作者信息

Gardiner R M

机构信息

Department of Paediatrics, University College, London, England.

出版信息

Am J Med Genet. 1992 Feb 15;42(4):539-41. doi: 10.1002/ajmg.1320420423.

Abstract

The ceroid-lipofuscinoses are a group of inherited neurodegenerative disorders characterised by the accumulation of autofluorescent lipopigment in neurones and other cell types. The underlying biochemical defect is unknown. Juvenile onset neuronal ceroid lipofuscinosis (Batten disease; Spielmeyer-Vogt disease) is an autosomal recessive trait. Linkage studies were undertaken to determine the location of the Batten disease (CLN3) mutation. Studies were carried out on 205 members of 42 families in which there were 76 affected individuals. Families originated from 7 North European countries and Canada. Serum samples from 23 families, including a total of 48 affected children, were tested for a set of "classical markers." A positive lod score was found with the haptoglobin (Hp) system. The combined male and female maximum lod score was 3.00 at theta = 0.00 and theta = 0.26, respectively. This provided an indication of localisation to the long arm of chromosome 16. Linkage analysis was then carried out in 42 families using DNA markers for loci on human chromosome 16. The maximal lod score between Batten disease and the locus D16S148 calculated for combined sexes was 6.05. No recombinants were observed. Multilocus analysis using 5 loci indicated the most likely order to be HP-D16S151-D16S150-CLN3-D16S148-D16S147. Work is in progress to refine the genetic and physical localisation of the Batten disease gene using additional markers in this region and a panel of somatic cell hybrids. Methods are now available which should allow the gene to be isolated and characterised.

摘要

蜡样脂褐质沉积症是一组遗传性神经退行性疾病,其特征是在神经元和其他细胞类型中积累自发荧光脂色素。潜在的生化缺陷尚不清楚。青少年型神经元蜡样脂褐质沉积症(巴顿病;施皮勒梅耶 - 福格特病)是一种常染色体隐性性状。进行连锁研究以确定巴顿病(CLN3)突变的位置。对42个家庭的205名成员进行了研究,其中有76名受影响个体。这些家庭来自7个北欧国家和加拿大。对23个家庭的血清样本(包括总共48名受影响儿童)进行了一组“经典标记”检测。在触珠蛋白(Hp)系统中发现了阳性连锁值。男性和女性的联合最大连锁值分别在θ = 0.00和θ = 0.26时为3.00。这表明该基因定位于16号染色体长臂。然后使用人类16号染色体上基因座的DNA标记对42个家庭进行连锁分析。计算得出巴顿病与基因座D16S148之间的联合性别最大连锁值为6.05。未观察到重组体。使用5个基因座的多位点分析表明最可能的顺序是HP - D16S151 - D16S150 - CLN3 - D16S148 - D16S147。目前正在进行相关工作,利用该区域的其他标记和一组体细胞杂种来完善巴顿病基因的遗传和物理定位。现在已有方法可以分离和鉴定该基因。

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