cGAS and CD-NTase enzymes: structure, mechanism, and evolution

被引:63
作者
Kranzusch, Philip J. [1 ,2 ,3 ]
机构
[1] Harvard Med Sch, Dept Microbiol, Boston, MA 02115 USA
[2] Dana Farber Canc Inst, Dept Canc Immunol & Virol, Boston, MA 02115 USA
[3] Dana Farber Canc Inst, Parker Inst Canc Immunotherapy, Boston, MA 02115 USA
关键词
CYCLIC GMP-AMP; DNA SENSOR; STING REVEALS; 2ND-MESSENGER; DINUCLEOTIDE; SYNTHASE; IDENTIFICATION; ACTIVATION; SURVEILLANCE; PROTEINS;
D O I
10.1016/j.sbi.2019.08.003
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cyclic GMP-AMP synthase (cGAS) is a signaling enzyme in human cells that controls immune-sensing of cytosolic DNA. The recent discoveries of diverse structural homologs of cGAS in animals and bacteria reveal that cGAS-like signaling is surprisingly ancient and widespread in biology. Together with the Vibrio cholerae protein dinucleotide cyclase in Vibrio (DncV), cGAS and DncV homologs comprise a family of cGAS/DncV-like nucleotidyltransferase (CD-NTase) enzymes that synthesize noncanonical RNA signals including cyclic dinucleotides, cyclic trinucleotides, and linear oligonucleotides. Structural and biochemical breakthroughs provide a framework to understand how CD-NTase signaling allows cells to respond to changing environmental conditions. The CD-NTase family also includes uncharacterized human genes like MB21D2 and Mab21L1, highlighting emerging functions of cGAS-like signaling beyond innate immunity.
引用
收藏
页码:178 / 187
页数:10
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