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岩藻糖苷贮积症中的一个5'剪接位点突变

A 5' splice site mutation in fucosidosis.

作者信息

Williamson M, Cragg H, Grant J, Kretz K, O'Brien J, Willems P J, Young E, Winchester B

机构信息

Division of Biochemistry and Metabolism, Institute of Child Health, London.

出版信息

J Med Genet. 1993 Mar;30(3):218-23. doi: 10.1136/jmg.30.3.218.

Abstract

Fucosidosis is a rare, autosomal recessive, lysosomal storage disease, resulting from a deficiency of the enzyme alpha-fucosidase (EC 3.2.1.51). It is characterised clinically by progressive mental and motor deterioration, growth retardation, coarse facies, and often recurrent infections, but the course of the disease is variable. The gene encoding lysosomal alpha-fucosidase has been mapped to the short arm of chromosome 1 at position 1p34.1-36.1 and has been called FUCA1. Two mutations causing disease have been described previously, a C-->T change in exon 8 giving rise to a premature, in frame TAA stop codon, and a deletion of at least two exons from the 3' end of the gene. In this paper we present evidence that a homozygous G-->A transition in the first position of the 5' splice site of intron 5 of FUCA1 is the disease causing mutation in a 9 year old child of distantly related parents. A new banding pattern was detected in the patient by Southern blotting of genomic DNA using TaqI restriction and a cDNA FUCA1 probe. The patient was homozygous for this pattern. Three sibs with alpha-fucosidase activity below the normal reference range and both parents were heterozygous. This pattern was not detected in 26 other fucosidosis patients and has not been found in any controls. The mutation was localised by a combination of restriction mapping using different cDNA probes, single stranded conformational polymorphism analysis of exons and flanking regions amplified by the polymerase chain reaction, and by direct sequencing of the amplified sequence. A view of the nature of the mutation, its cosegregation with the disease mutation and its absence in controls, it is probable that the 5' splice site mutation causes fucosidosis in this child.

摘要

岩藻糖苷贮积症是一种罕见的常染色体隐性溶酶体贮积病,由α-岩藻糖苷酶(EC 3.2.1.51)缺乏所致。其临床特征为进行性智力和运动功能衰退、生长发育迟缓、面容粗糙,且常反复感染,但疾病进程因人而异。编码溶酶体α-岩藻糖苷酶的基因已被定位于1号染色体短臂1p34.1 - 36.1位置,命名为FUCA1。此前已描述了两个致病突变,外显子8中的C→T改变导致一个过早的框内TAA终止密码子,以及基因3'端至少两个外显子的缺失。在本文中,我们提供证据表明,FUCA1基因内含子5的5'剪接位点第一个位置的纯合G→A转换是一名远亲父母所生9岁儿童的致病突变。使用TaqI酶切和cDNA FUCA1探针通过基因组DNA的Southern印迹法在患者中检测到一种新的条带模式。该患者对此模式为纯合子。三名α-岩藻糖苷酶活性低于正常参考范围的同胞以及父母均为杂合子。在其他26例岩藻糖苷贮积症患者中未检测到这种模式,在任何对照中也未发现。通过使用不同cDNA探针的限制性图谱分析、聚合酶链反应扩增的外显子及其侧翼区域的单链构象多态性分析以及扩增序列的直接测序相结合的方法确定了该突变的位置。鉴于该突变的性质、其与致病突变的共分离情况以及在对照中不存在,很可能这个5'剪接位点突变导致了该儿童的岩藻糖苷贮积症。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/15b6/1016303/d7256086193b/jmedgene00005-0047-a.jpg

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