PARG Protein Regulation Roles in Drosophila Longevity Control

Guillaume Bordet, A. Tulin
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Abstract

Aging, marked by a gradual decline in physiological function and heightened vulnerability to age-related diseases, remains a complex biological process with multifaceted regulatory mechanisms. Our study elucidates the critical role of poly(ADP–ribose) glycohydrolase (PARG), responsible for catabolizing poly(ADP–ribose) (pADPr) in the aging process by modulating the expression of age-related genes in Drosophila melanogaster. Specifically, we uncover the regulatory function of the uncharacterized PARG C-terminal domain in controlling PARG activity. Flies lacking this domain exhibit a significantly reduced lifespan compared to wild-type counterparts. Furthermore, we observe progressive dysregulation of age-related gene expression during aging, accelerated in the absence of PARG activity, culminating in a premature aging phenotype. Our findings reveal the critical involvement of the pADPr pathway as a key player in the aging process, highlighting its potential as a therapeutic target for mitigating age-related effects.
PARG 蛋白在果蝇长寿控制中的调控作用
衰老以生理功能逐渐衰退和更易患老年相关疾病为特征,它仍然是一个具有多方面调控机制的复杂生物过程。我们的研究阐明了负责分解聚(ADP-核糖)(pADPr)的聚(ADP-核糖)糖水解酶(PARG)通过调节黑腹果蝇中与年龄相关基因的表达在衰老过程中的关键作用。具体来说,我们发现了未表征的 PARG C 端结构域在控制 PARG 活性方面的调控功能。与野生型果蝇相比,缺乏该结构域的果蝇寿命明显缩短。此外,我们还观察到在衰老过程中,与年龄相关的基因表达逐渐失调,在 PARG 活性缺失的情况下会加速,最终形成早衰表型。我们的研究结果揭示了 pADPr 通路在衰老过程中的关键作用,并强调了其作为减轻衰老相关影响的治疗靶点的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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