Division of Gastroenterology, Box 8124, Washington University School of Medicine, 660 Euclid Avenue, St. Louis, MO 63110, USA.
Hepatology. 2010 Mar;51(3):1055-61. doi: 10.1002/hep.23344.
Posttranscriptional regulation of gene expression is increasingly recognized as a model for inherited and acquired disease. Recent work has expanded understanding of the range of mechanisms that regulate several of these distinct steps, including messenger RNA (mRNA) splicing, trafficking, and/or stability. Each of these pathways is implicated in disease pathogenesis, and each represents important avenues for therapeutic intervention. This review summarizes important mechanisms controlling mRNA processing and the regulation of mRNA degradation, including the role of microRNAs and RNA binding proteins. These pathways provide important opportunities for therapeutic targeting directed at splicing and degradation in order to attenuate genetic defects in RNA metabolism. We will highlight developments in vector development and validation for therapeutic manipulation of mRNA expression with a focus on potential applications in metabolic and immunomediated liver disease.
基因表达的转录后调控正逐渐被视为遗传和获得性疾病的一种模型。最近的研究扩大了人们对调节这些不同步骤的多种机制的理解,包括信使 RNA(mRNA)剪接、运输和/或稳定性。这些途径中的每一个都与疾病的发病机制有关,并且每一个都代表了治疗干预的重要途径。本综述总结了控制 mRNA 加工和 mRNA 降解调节的重要机制,包括 microRNAs 和 RNA 结合蛋白的作用。这些途径为靶向剪接和降解提供了重要的治疗机会,以减轻 RNA 代谢中遗传缺陷。我们将重点介绍载体开发和验证方面的进展,以实现对 mRNA 表达的治疗性操纵,特别关注代谢和免疫介导的肝脏疾病的潜在应用。