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Structural basis for the inhibition of cGAS by nucleosomes
Author(s) -
Tomoya Kujirai,
Christian Zierhut,
Yoshimasa Takizawa,
Ryan Kim,
Lumi Negishi,
Nobuki Uruma,
Seiya Hirai,
Hironori Funabiki,
Hitoshi Kurumizaka
Publication year - 2020
Publication title -
science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 12.556
H-Index - 1186
eISSN - 1095-9203
pISSN - 0036-8075
DOI - 10.1126/science.abd0237
Subject(s) - nucleosome , chromatin , dna , microbiology and biotechnology , cytosol , chemistry , guanosine , biophysics , biochemistry , biology , enzyme
Saving a host cell from itself A fundamental mammalian defense mechanism against pathogens and damaged cellular DNA is to recognize DNA fragments in the cytosol and trigger an inflammatory response. The cyclic guanosine monophosphate–adenosine monophosphate synthase (cGAS) that recognizes cytosolic DNA is also found in the nucleus, but here its activity is suppressed by tethering to chromatin. Two papers now report cryo–electron microscopy structures of cGAS bound to the nucleosome core particle (NCP). Kujiraiet al. observed a structure with two cGAS molecules bridging two NCPs, whereas Boyeret al. observed cGAS bound to a single nucleosome. Together, these structures show how cGAS is prevented from autoreactivity toward host DNA.Science , this issue p.455 , p.450

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