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Alternative splicing in aging and age-related diseases

机译:衰老和与年龄有关的疾病的替代拼接

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Alternative splicing (AS) of mRNA generates multiple protein isoforms from a single gene. This greatly expands proteome diversity and plays important roles in most biological processes. Global changes occur to AS as cells and individuals age normally and during age-related diseases. Some of these changes play critical roles in aging and associated phenotypes. Although AS has been extensively reviewed with respect to functions and molecular mechanisms in certain biological processes, a comprehensive view of AS is lacking in aging research. In this review, we focus on the functional side of AS in the aging process, and we summarize the age-related genes and splicing types, the potential functional mechanisms, upstream regulators and pathways involved. Global changes to AS during aging and potential therapeutic strategies to correct aberrant splicing are also discussed.
机译:mRNA的选择性剪接(AS)可从单个基因产生多种蛋白质同工型。这极大地扩展了蛋白质组多样性,并在大多数生物过程中发挥了重要作用。随着细胞和个体正常衰老以及在与年龄有关的疾病期间,AS发生全局变化。这些变化中的一些在衰老和相关表型中起关键作用。尽管对AS在某些生物学过程中的功能和分子机制进行了广泛的审查,但在衰老研究中仍缺乏对AS的全面了解。在这篇综述中,我们着重于AS在衰老过程中的功能方面,并总结了与年龄相关的基因和剪接类型,潜在的功能机制,上游调控因子和所涉及的途径。还讨论了衰老过程中AS的总体变化以及纠正异常剪接的潜在治疗策略。

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