Bonini Nancy M, La Spada Albert R
Department of Biology and University of Pennsylvania, Philadelphia, Pennsylvania 19104, USA.
Neuron. 2005 Dec 8;48(5):715-8. doi: 10.1016/j.neuron.2005.11.008.
Nine dominantly inherited neurodegenerative diseases are caused by expansion of a CAG repeat encoding glutamine. An important development in the study of such "polyglutamine" diseases was the realization that merely shutting off expression of a disease-encoding transgene could arrest progression in animal models with significant disease pathology. Such studies opened the door to a powerful new therapeutic approach now being pioneered: silencing of the dominant disease allele by RNA-mediated interference (RNAi), for the arrest--and potential reversal--of the disease process.
九种显性遗传神经退行性疾病是由编码谷氨酰胺的CAG重复序列扩增引起的。在这类“多聚谷氨酰胺”疾病的研究中,一项重要进展是认识到仅仅关闭致病转基因的表达就可以在具有显著疾病病理的动物模型中阻止疾病进展。此类研究为一种正在开创的强大新治疗方法打开了大门:通过RNA介导的干扰(RNAi)使显性疾病等位基因沉默,以阻止——并可能逆转——疾病进程。