Regulation of cGAS Activity and Downstream Signaling.

Bhagwati Joshi, Jagdish Chandra Joshi, Dolly Mehta

Journal: Cells 2022;11(18):2812

PMID: 36139387

Abstract

Cyclic GMP-AMP synthase (cGAS) is a predominant and ubiquitously expressed cytosolic onfirmedDNA sensor that activates innate immune responses by producing a second messenger, cyclic GMP-AMP (cGAMP), and the stimulator of interferon genes (STING). cGAS contains a highly disordered N-terminus, which can sense genomic/chromatin DNA, while the C terminal of cGAS binds dsDNA liberated from various sources, including mitochondria, pathogens, and dead cells. Furthermore, cGAS cellular localization dictates its response to foreign versus self-DNA. Recent evidence has also highlighted the importance of dsDNA-induced post-translational modifications of cGAS in modulating inflammatory responses. This review summarizes and analyzes cGAS activity regulation based on structure, sub-cellular localization, post-translational mechanisms, and Ca signaling. We also discussed the role of cGAS activation in different diseases and clinical outcomes.

Address: Department of Pharmacology and Regenerative Medicine, College of Medicine, University of Illinois, 835 S Wolcott Avenue, Chicago, IL 60612, USA.
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