了解长寿:揭示 SIN-3 和 DAF-16 在寿命调节中的独立作用

Chandrika Konwar, Jayant Maini, Daman Saluja
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摘要

衰老是生理生化逐渐退化的过程。虽然衰老不可避免,但健康的衰老是个人和社会福祉的关键。因此,了解衰老的调控至关重要。SIN-3/Sin3 是一种独特的调控蛋白,它在没有 DNA 结合活性的情况下调控衰老。它通过建立多种蛋白质相互作用来发挥作用。为了了解这种转录调控因子的功能机制,我们评估了草履虫蛋白质相互作用组中 SIN-3 的相互作用。DAF-16/FOXO 成为 SIN-3 介导的衰老调控的主要竞争者之一。本研究探讨了 SIN-3 和 DAF-16 蛋白在寿命调控中的协同作用。对这些基因的突变体进行的表型分析表明,这两种蛋白在应激反应和重要生物过程中具有相似的功能。然而,在检测SIN-3和DAF-16蛋白之间的蛋白质相互作用时,并没有发现明显的物理相互作用。秀丽隐杆线虫基因组学和转录组学数据也表明了基因协同调控的可能性。这种基因调控更有可能与 SIN-3 对 DAF-16 功能的支配作用有关。总之,SIN-3 和 DAF-16 蛋白具有很强的功能相互作用,可确保健康老化。SIN-3 对 DAF-16 介导的应激反应的影响是它们在长寿调控方面的交汇点之一。
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Understanding Longevity: SIN-3 and DAF-16 Revealed as Independent Players in Lifespan Regulation.

Aging is the process of gradual physio-biochemical deterioration. Although aging is inevitable, healthy aging is the key to individual and communal well-being. Therefore, it is essential to understand the regulation of aging. SIN-3/Sin-3 is a unique regulatory protein that regulates aging without DNA-binding activity. It functions by establishing multiple protein interactions. To understand the functional mechanism of this transcriptional regulator, the Caenorhabditis elegans protein interactome was assessed for SIN-3 interactions. DAF-16/FOXO emerged as one of the leading contenders for SIN-3-mediated regulation of aging. This study looks at the concerted role of SIN-3 and DAF-16 proteins in lifespan regulation. Phenotypic profiling for the mutants of these genes shows the functional accord between these 2 proteins with similar functions in stress response and vital biological processes. However, there were no significant physical interactions when checked for protein-protein interaction between SIN-3 and DAF-16 proteins. C. elegans genomics and transcriptomics data also indicated the possibilities of concerted gene regulation. This genetic regulation is more likely related to SIN-3 dominance on DAF-16 function. Overall, SIN-3 and DAF-16 proteins have strong functional interactions that ensure healthy aging. The influence of SIN-3 on DAF-16-mediated stress response is one of their convergence points in longevity regulation.

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