一种SCN9A通道病变导致先天性无法体验疼痛
James J Cox1, Frank Reimann, Adeline K Nicholas
1Department of Medical Genetics, Cambridge Institute for Medical Research, Wellcome/MRC Building, Addenbrooke's Hospital, Cambridge CB2 0XY, UK.
Nature
|December 15, 2006
概括
完全无法感觉到疼痛的个体有一个罕见的遗传疾病. 这项研究确定了SCN9A基因中的三个新奇突变,这对疼痛信号至关重要,解释了这种疼痛不敏感.
科学领域:
- 遗传学 遗传学 是一个
- 神经科学是一个神经科学.
- 分子生物学分子生物学
背景情况:
- 对疼痛的先天不敏感是一种极其罕见的疾病.
- 疼痛感知主要由称为感觉受体的专门感觉神经元进行介导.
研究的目的:
- 调查三个巴基斯坦家庭内先天性疼痛不敏感的遗传基础.
- 为了确定负责失去疼痛感觉的特定基因和突变.
主要方法:
- 全基因组链接分析将致病基因映射到2q24.3.3.染色体上
- 在受影响个体中,SCN9A基因的桑格测序.
- 在HEK293细胞中使用异质表达的识别SCN9A突变的功能性表征.
主要成果:
- 在受影响个体的SCN9A基因中确定了三种不同的同卵性无意义突变 (S459X,I767X,W897X).
- 已经证明,这些突变导致Na(v) 1.7通道的功能完全丧失.
- 在表达突变Na(v) 1.7通道的细胞中没有观察到可测量的离子通道活性.
结论:
- 编码Na(v) 1.7通道的SCN9A基因对于人类的知觉是必不可少的,并且不是多余的.
- 在SCN9A中的功能丧失突变会导致先天性疼痛不敏感.
- 这些发现为开发针对Na(v) 1.7通道的新型止痛药提供了基础.
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