Cyclic GMP-AMP synthase recognizes the physical features of DNA.

IF 6.9 1区 医学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Acta Pharmacologica Sinica Pub Date : 2025-02-01 Epub Date: 2024-08-07 DOI:10.1038/s41401-024-01369-7
Ling Dong, Yue-Ru Hou, Na Xu, Xiao-Qian Gao, Zhen Sun, Qing-Kai Yang, Li-Na Wang
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引用次数: 0

Abstract

Cyclic GMP-AMP synthase (cGAS) is a major cytosolic DNA sensor that plays a significant role in innate immunity. Upon binding to double stranded DNA (dsDNA), cGAS utilizes GTP and ATP to synthesize the second messenger cyclic GMP-AMP (cGAMP). The cGAMP then binds to the adapter protein stimulator of interferon genes (STING) in the endoplasmic reticulum, resulting in the activation of the transcription factor interferon regulatory factor 3 (IRF3) and subsequent induction of type I interferon. An important question is how cGAS distinguishes between self and non-self DNA. While cGAS binds to the phosphate backbone of DNA without discrimination, its activation is influenced by physical features such as DNA length, inter-DNA distance, and mechanical flexibility. This suggests that the recognition of DNA by cGAS may depend on these physical features. In this article we summarize the recent progress in research on cGAS-STING pathway involved in antiviral defense, cellular senescence and anti-tumor response, and focus on DNA recognition mechanisms based on the physical features.

Abstract Image

环状 GMP-AMP 合成酶能识别 DNA 的物理特征。
环GMP-AMP合成酶(cGAS)是一种主要的细胞膜DNA传感器,在先天性免疫中发挥着重要作用。与双链 DNA(dsDNA)结合后,cGAS 利用 GTP 和 ATP 合成第二信使环 GMP-AMP (cGAMP)。然后,cGAMP 与内质网中的适配蛋白干扰素基因刺激因子(STING)结合,导致转录因子干扰素调节因子 3(IRF3)被激活,进而诱导产生 I 型干扰素。一个重要的问题是 cGAS 如何区分自体和非自体 DNA。虽然 cGAS 能无差别地与 DNA 的磷酸骨架结合,但它的激活会受到 DNA 长度、DNA 间距和机械灵活性等物理特征的影响。这表明,cGAS 对 DNA 的识别可能取决于这些物理特征。在本文中,我们总结了参与抗病毒防御、细胞衰老和抗肿瘤反应的 cGAS-STING 通路的最新研究进展,并重点探讨了基于物理特征的 DNA 识别机制。
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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来源期刊
Acta Pharmacologica Sinica
Acta Pharmacologica Sinica 医学-化学综合
CiteScore
15.10
自引率
2.40%
发文量
4365
审稿时长
2 months
期刊介绍: APS (Acta Pharmacologica Sinica) welcomes submissions from diverse areas of pharmacology and the life sciences. While we encourage contributions across a broad spectrum, topics of particular interest include, but are not limited to: anticancer pharmacology, cardiovascular and pulmonary pharmacology, clinical pharmacology, drug discovery, gastrointestinal and hepatic pharmacology, genitourinary, renal, and endocrine pharmacology, immunopharmacology and inflammation, molecular and cellular pharmacology, neuropharmacology, pharmaceutics, and pharmacokinetics. Join us in sharing your research and insights in pharmacology and the life sciences.
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