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一个患有致密性骨发育不全的巴基斯坦近亲家庭中,组织蛋白酶K(CTSK)基因发生了一种新的错义突变。

A novel missense mutation in cathepsin K (CTSK) gene in a consanguineous Pakistani family with pycnodysostosis.

作者信息

Khan Bushra, Ahmed Zahoor, Ahmad Wasim

机构信息

Department of Biochemistry, Quaid-i-Azam University, Islamabad, Pakistan.

出版信息

J Investig Med. 2010 Jun;58(5):720-4. doi: 10.231/JIM.0b013e3181da50bd.

Abstract

BACKGROUND

Deficiency of cathepsin K (CTSK), a lysosomal cysteine protease, has been shown earlier as a cause of an autosomal recessive osteosclerotic skeletal dysplasia pycnodysostosis. The objective of the present study was to identify the potential sequence variants in CTSK gene in a large consanguineous Pakistani family with pycnodysostosis.

METHODS

Genotyping of 4 affected and 6 unaffected members of the family was performed using polymorphic microsatellite markers linked to CTSK gene on chromosome 1q21. To screen for pathogenic mutation, exons and splice junctions of CTSK gene were polymerase chain reaction amplified from genomic DNA and sequenced directly in an automated DNA sequencer.

RESULTS

Microsatellite analysis showed linkage of the family to CTSK gene on chromosome 1q21. Sequence analysis revealed a novel missense mutation c.728G>A (p.G243E) in exon 6 of the CTSK gene.

CONCLUSIONS

A novel missense mutation was identified in CTSK gene in a Pakistani family with 5 individuals affected with autosomal recessive pycnodysostosis.

摘要

背景

组织蛋白酶K(CTSK)是一种溶酶体半胱氨酸蛋白酶,此前已证实其缺乏是常染色体隐性骨硬化性骨骼发育不良——致密性成骨不全症的病因。本研究的目的是在一个患有致密性成骨不全症的巴基斯坦近亲家庭中鉴定CTSK基因的潜在序列变异。

方法

使用与1号染色体q21上CTSK基因相关的多态性微卫星标记,对该家庭中4名患病成员和6名未患病成员进行基因分型。为筛查致病突变,从基因组DNA中通过聚合酶链反应扩增CTSK基因的外显子和剪接连接点,并直接在自动DNA测序仪中进行测序。

结果

微卫星分析显示该家庭与1号染色体q21上CTSK基因存在连锁关系。序列分析在CTSK基因外显子6中发现了一个新的错义突变c.728G>A(p.G243E)。

结论

在一个有5名个体患常染色体隐性致密性成骨不全症的巴基斯坦家庭中,CTSK基因鉴定出一个新的错义突变。

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