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化学遗传学与罕见遗传病

Chemical genetics and orphan genetic diseases.

作者信息

Lunn Mitchell R, Stockwell Brent R

机构信息

Department of Biological Sciences, Sherman Fairchild Center for the Life Sciences, Columbia University, New York, New York 10027, USA.

出版信息

Chem Biol. 2005 Oct;12(10):1063-73. doi: 10.1016/j.chembiol.2005.09.005.

Abstract

Many orphan diseases have been identified that individually affect small numbers of patients but cumulatively affect approximately 6%-10% of the European and United States populations. Human genetics has become increasingly effective at identifying genetic defects underlying such orphan genetic diseases, but little progress has been made toward understanding the causal molecular pathologies and creating targeted therapies. Chemical genetics, positioned at the interface of chemistry and genetics, can be used for elucidation of molecular mechanisms underlying diseases and for drug discovery. This review discusses recent advances in chemical genetics and how small-molecule tools can be used to study and ultimately treat orphan genetic diseases. We focus here on a case study involving spinal muscular atrophy, a pediatric neurodegenerative disease caused by homozygous deletion of the SMN1 (survival of motor neuron 1) gene.

摘要

许多罕见病已被确认,这些疾病单独影响的患者数量较少,但累计影响约6% - 10%的欧美人口。人类遗传学在识别此类罕见遗传病背后的基因缺陷方面越来越有效,但在理解致病分子病理学和开发靶向治疗方面进展甚微。化学遗传学处于化学与遗传学的交叉领域,可用于阐明疾病背后的分子机制以及药物研发。本综述讨论了化学遗传学的最新进展,以及小分子工具如何用于研究并最终治疗罕见遗传病。我们在此聚焦于一个涉及脊髓性肌萎缩症的案例研究,这是一种由SMN1(运动神经元存活1)基因纯合缺失引起的儿童神经退行性疾病。

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