RNA Therapeutics Institute, University of Massachusetts Medical School, Worcester, Massachusetts.
Center for Molecular Medicine and Genetics, and Department of Obstetrics and Gynecology, Wayne State University, Detroit, Michigan.
Wiley Interdiscip Rev RNA. 2019 Jan;10(1):e1503. doi: 10.1002/wrna.1503. Epub 2018 Sep 14.
RNA processing has emerged as a key mechanistic step in the regulation of the cellular response to environmental perturbation. Recent work has uncovered extensive remodeling of transcriptome composition upon environmental perturbation and linked the impacts of this molecular plasticity to health and disease outcomes. These isoform changes and their underlying mechanisms are varied-involving alternative sites of transcription initiation, alternative splicing, and alternative cleavage at the 3' end of the mRNA. The mechanisms and consequences of differential RNA processing have been characterized across a range of common environmental insults, including chemical stimuli, immune stimuli, heat stress, and cancer pathogenesis. In each case, there are perturbation-specific contributions of local (cis) regulatory elements or global (trans) factors and downstream consequences. Overall, it is clear that choices in isoform usage involve a balance between the usage of specific genetic elements (i.e., splice sites, polyadenylation sites) and the timing at which certain decisions are made (i.e., transcription elongation rate). Fine-tuned cellular responses to environmental perturbation are often dependent on the genetic makeup of the cell. Genetic analyses of interindividual variation in splicing have identified genetic effects on splicing that contribute to variation in complex traits. Finally, the increase in the number of tissue types and environmental conditions analyzed for RNA processing is paralleled by the need to develop appropriate analytical tools. The combination of large datasets, novel methods and conditions explored promises to provide a much greater understanding of the role of RNA processing response in human phenotypic variation. This article is categorized under: RNA Processing > RNA Editing and Modification RNA Evolution and Genomics > Computational Analyses of RNA RNA Processing > Splicing Mechanisms RNA Processing > Splicing Regulation/Alternative Splicing.
RNA 处理已成为调节细胞对外界环境干扰反应的关键机制步骤。最近的研究揭示了环境干扰后转录组组成的广泛重构,并将这种分子可塑性的影响与健康和疾病结果联系起来。这些异构体的变化及其潜在机制是多种多样的,涉及转录起始的替代位点、选择性剪接和 mRNA 3'端的选择性切割。已经在一系列常见的环境刺激物(包括化学刺激物、免疫刺激物、热应激和癌症发病机制)中对差异 RNA 处理的机制和后果进行了特征描述。在每种情况下,都有局部(顺式)调节元件或全局(反式)因子的特定干扰贡献及其下游后果。总的来说,很明显,异构体使用的选择涉及到特定遗传元件(即剪接位点、多聚腺苷酸化位点)的使用与某些决策(即转录延伸率)做出的时间之间的平衡。对环境干扰的精细细胞反应通常取决于细胞的遗传组成。对剪接个体间变异的遗传分析已经确定了对剪接有影响的遗传效应,这些效应有助于复杂性状的变异。最后,分析 RNA 处理的组织类型和环境条件的数量增加,需要开发适当的分析工具。大量数据集、新方法和探索的条件的结合有望提供对 RNA 处理反应在人类表型变异中的作用的更深入理解。本文属于以下类别:RNA 处理 > RNA 编辑和修饰 RNA 进化和基因组学 > RNA 的计算分析 RNA 处理 > 剪接机制 RNA 处理 > 剪接调控/选择性剪接。