Phosphorylation and chromatin tethering prevent cGAS activation during mitosis

Author:

Li Tuo123ORCID,Huang Tuozhi12ORCID,Du Mingjian12ORCID,Chen Xiang123ORCID,Du Fenghe123ORCID,Ren Junyao12ORCID,Chen Zhijian J.123ORCID

Affiliation:

1. Department of Molecular Biology, University of Texas Southwestern Medical Center, Dallas, TX 75390-9148, USA.

2. Center for Inflammation Research, University of Texas Southwestern Medical Center, Dallas, TX 75390-9148, USA.

3. Howard Hughes Medical Institute, University of Texas Southwestern Medical Center, Dallas, TX 75390-9148, USA.

Abstract

Keeping cGAS silent Cells detect microbial and self-DNA in the cytosol as a danger signal that triggers immune and inflammatory responses. Paradoxically, a large fraction of a DNA-sensing enzyme called cGAS is tightly associated with the chromatin, especially during mitosis. Li et al. uncovered two mechanisms that prevent cGAS from being activated by the chromatin DNA (see the Perspective by Ablasser). First, cGAS is hyperphosphorylated as cells enter mitosis, thereby inhibiting its DNA-binding and liquid-liquid phase separation, which promotes cGAS activation. Second, chromatin-bound cGAS is unable to oligomerize, a process required for its activation. Together, these mechanisms ensure cGAS inactivation during cell division to prevent autoimmune reactions. Science , this issue p. eabc5386 ; see also p. 1204

Funder

Howard Hughes Medical Institute

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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