Zhang Nan, Ashizawa Tetsuo
Neurosciences Research Program, Houston Methodist Research Institute, Houston, TX 77030, United States; Division of Cell and Molecular Biology, South Kensington Campus, Imperial College London, London SW7 2AZ, UK.
Neurosciences Research Program, Houston Methodist Research Institute, Houston, TX 77030, United States.
Curr Opin Genet Dev. 2017 Jun;44:17-29. doi: 10.1016/j.gde.2017.01.005. Epub 2017 Feb 14.
More than 30 incurable neurological and neuromuscular diseases are caused by simple microsatellite expansions consisted of 3-6 nucleotides. These repeats can occur in non-coding regions and often result in a dominantly inherited disease phenotype that is characteristic of a toxic RNA gain-of-function. The expanded RNA adopts unusual secondary structures, sequesters various RNA binding proteins to form insoluble nuclear foci, and causes cellular defects at a multisystem level. Nuclear foci are dynamic in size, shape and colocalization of RNA binding proteins in different expansion diseases and tissue types. This review sets to provide new insights into the disease mechanisms of RNA toxicity and foci modulation, in light of recent advancement on bi-directional transcription, antisense RNA, repeat-associated non-ATG translation and beyond.
超过30种无法治愈的神经和神经肌肉疾病是由由3-6个核苷酸组成的简单微卫星扩张引起的。这些重复序列可出现在非编码区,常导致显性遗传疾病表型,其特征为毒性RNA功能获得。扩展的RNA采用异常的二级结构,隔离各种RNA结合蛋白以形成不溶性核灶,并在多系统水平上导致细胞缺陷。在不同的扩张性疾病和组织类型中,核灶在RNA结合蛋白的大小、形状和共定位方面是动态变化的。鉴于双向转录、反义RNA、重复相关非ATG翻译等方面的最新进展,本综述旨在为RNA毒性和病灶调节的疾病机制提供新的见解。