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阿根廷桑德霍夫病患者中两个HEXB基因突变的特征分析。

Characterization of two HEXB gene mutations in Argentinean patients with Sandhoff disease.

作者信息

Brown C A, McInnes B, de Kremer R D, Mahuran D J

机构信息

Research Institute, Hospital for Sick Children, Toronto, Ontario, Canada.

出版信息

Biochim Biophys Acta. 1992 Oct 13;1180(1):91-8. doi: 10.1016/0925-4439(92)90031-h.

Abstract

Beta-hexosaminidase A (beta-N-acetyl-D-hexosaminidase, EC 3.2.1.5.2) is a lysosomal hydrolase composed of an alpha- and a beta-subunit. It is responsible for the degradation of GM2 ganglioside. Mutations in the HEXB gene encoded beta-subunit cause a form of GM2 gangliosidosis known as Sandhoff disease. Although this is a rare disease in the general population, several geographically isolated groups have a high carrier frequency. Most notably, a 1 in 16-29 carrier frequency has been reported for an Argentinean population living in an area contained within a 375-km radius from Córdoba. Analysis of the genomic DNA of two patients from this region revealed that one was homozygous for a G to A substitution at the 5' donor splice site of intron 2. This mutation completely abolishes normal mRNA splicing. The other patient was a compared of the intron 2 G-->A substitution and a second allele due to a 4-bp deletion in exon 7. The beta-subunit mRNA of this allele is unstable, presumably as a result of an early stop codon introduced by the deletion. Two novel PCR-based assays were developed to detect these mutations. We suggest that one of these assays could be modified and used as a rapid screening procedure for 5' donor splice site defects in other genes. These results provide a further example of the genetic heterogeneity that can exist even in a small geographically isolated population.

摘要

β - 己糖胺酶A(β - N - 乙酰 - D - 己糖胺酶,EC 3.2.1.5.2)是一种由α亚基和β亚基组成的溶酶体水解酶。它负责GM2神经节苷脂的降解。编码β亚基的HEXB基因突变会导致一种称为桑德霍夫病的GM2神经节苷脂贮积症。虽然这在普通人群中是一种罕见疾病,但几个地理上隔离的群体有较高的携带者频率。最值得注意的是,据报道,居住在距科尔多瓦半径375公里范围内地区的阿根廷人群中,携带者频率为1/16 - 29。对该地区两名患者的基因组DNA分析显示,其中一名患者在第2内含子的5'供体剪接位点发生了G到A的纯合替代。这种突变完全消除了正常的mRNA剪接。另一名患者是第2内含子G→A替代与外显子7中4个碱基缺失导致的第二个等位基因的杂合子。该等位基因的β亚基mRNA不稳定,可能是由于缺失引入了早期终止密码子。开发了两种基于PCR的新检测方法来检测这些突变。我们建议可以对其中一种检测方法进行修改,并将其用作其他基因5'供体剪接位点缺陷的快速筛查程序。这些结果进一步证明了即使在一个地理上隔离的小群体中也可能存在遗传异质性。

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