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cGAS and CD-NTase enzymes: structure, mechanism, and evolution
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 th...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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The Author. Published by Elsevier Ltd.
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7127440/ https://www.ncbi.nlm.nih.gov/pubmed/31593902 http://dx.doi.org/10.1016/j.sbi.2019.08.003 |
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author | Kranzusch, Philip J |
author_facet | Kranzusch, Philip J |
author_sort | Kranzusch, Philip J |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-7127440 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | The Author. Published by Elsevier Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71274402020-04-08 cGAS and CD-NTase enzymes: structure, mechanism, and evolution Kranzusch, Philip J Curr Opin Struct Biol Article 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. The Author. Published by Elsevier Ltd. 2019-12 2019-10-06 /pmc/articles/PMC7127440/ /pubmed/31593902 http://dx.doi.org/10.1016/j.sbi.2019.08.003 Text en © 2019 The Author Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Kranzusch, Philip J cGAS and CD-NTase enzymes: structure, mechanism, and evolution |
title | cGAS and CD-NTase enzymes: structure, mechanism, and evolution |
title_full | cGAS and CD-NTase enzymes: structure, mechanism, and evolution |
title_fullStr | cGAS and CD-NTase enzymes: structure, mechanism, and evolution |
title_full_unstemmed | cGAS and CD-NTase enzymes: structure, mechanism, and evolution |
title_short | cGAS and CD-NTase enzymes: structure, mechanism, and evolution |
title_sort | cgas and cd-ntase enzymes: structure, mechanism, and evolution |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7127440/ https://www.ncbi.nlm.nih.gov/pubmed/31593902 http://dx.doi.org/10.1016/j.sbi.2019.08.003 |
work_keys_str_mv | AT kranzuschphilipj cgasandcdntaseenzymesstructuremechanismandevolution |