G蛋白结合受体 (GPCR) 基因变异和人类遗传疾病
Miles D Thompson1, Maire E Percy2, David E C Cole3
1Krembil Brain Institute, Toronto Western Hospital, Toronto, ON, Canada.
Critical reviews in clinical laboratory sciences
|March 18, 2024
概括
在G蛋白结合受体 (GPCRs) 的遗传变异导致人类疾病. 先进的测序可以识别不确定的变异,帮助药物开发和精确医学治疗各种疾病.
科学领域:
- 遗传学和分子生物学
- 药理学 药理学是指药理学的学科.
- 人类疾病遗传学 人类疾病遗传学
背景情况:
- G蛋白结合受体 (GPCR) 的遗传变异与超过66种人类单一性疾病有关.
- 这些变异可以导致功能丧失或功能增加,影响受体信号传递,带结合和蛋白质相互作用.
研究的目的:
- 审查引起疾病的GPCR变体,并讨论变体解释的计算策略.
- 突出GPCR变异在药物开发和精准医学中的作用.
主要方法:
- 关于GPCR变体和相关疾病的文献综述.
- 讨论用于变异显著性评估的 in silico 工具 (例如,SIFT,PolyPhen).
- 用GPCR变异驱动的治疗干预措施的例子.
主要成果:
- 至少55个GPCR的致病变体与人类遗传疾病有关.
- 形方法有助于分类具有不确定的意义的变异 (VUS).
- 感受受体 (CaSR),黑色皮质素受体和其他GPCR变异具有治疗意义.
结论:
- 在理解单一性疾病和开发向疗法的过程中,GPCR变异至关重要.
- 下一代测序继续揭示具有潜在治疗价值的新型GPCR变异.
- 对GPCR变异的研究为理解药物遗传变异提供了基础.
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