dc.contributor.author | Hillebrand, Roman | |
dc.contributor.author | Sassanfar, Mandana | |
dc.contributor.author | Dedon, Peter C. | |
dc.date.accessioned | 2020-05-12T17:42:33Z | |
dc.date.available | 2020-05-12T17:42:33Z | |
dc.date.issued | 2019-11 | |
dc.identifier.issn | 2041-1723 | |
dc.identifier.uri | https://hdl.handle.net/1721.1/125185 | |
dc.description.abstract | Genome modifications are central components of the continuous arms race between viruses and their hosts. The archaeosine base (G+), which was thought to be found only in archaeal tRNAs, was recently detected in genomic DNA of Enterobacteria phage 9g and was proposed to protect phage DNA from a wide variety of restriction enzymes. In this study, we identify three additional 2′-deoxy-7-deazaguanine modifications, which are all intermediates of the same pathway, in viruses: 2′-deoxy-7-amido-7-deazaguanine (dADG), 2′-deoxy-7-cyano-7-deazaguanine (dPreQ0) and 2′-deoxy-7- aminomethyl-7-deazaguanine (dPreQ1). We identify 180 phages or archaeal viruses that encode at least one of the enzymes of this pathway with an overrepresentation (60%) of viruses potentially infecting pathogenic microbial hosts. Genetic studies with the Escherichia phage CAjan show that DpdA is essential to insert the 7-deazaguanine base in phage genomic DNA and that 2′-deoxy-7-deazaguanine modifications protect phage DNA from host restriction enzymes. | en_US |
dc.description.sponsorship | National Institutes of Health (U.S.) (Grant GM70641) | en_US |
dc.language.iso | en | |
dc.publisher | Springer Science and Business Media LLC | en_US |
dc.relation.isversionof | 10.1038/s41467-019-13384-y | en_US |
dc.rights | Creative Commons Attribution 4.0 International license | en_US |
dc.rights.uri | https://creativecommons.org/licenses/by/4.0/ | en_US |
dc.source | Nature | en_US |
dc.title | 7-Deazaguanine modifications protect phage DNA from host restriction systems | en_US |
dc.type | Article | en_US |
dc.identifier.citation | Hutinet, Geoffrey et al. “7-Deazaguanine modifications protect phage DNA from host restriction systems.” Nature Communications 10 (2019): 5442 © 2019 The Author(s) | en_US |
dc.contributor.department | Massachusetts Institute of Technology. Department of Biological Engineering | en_US |
dc.contributor.department | Massachusetts Institute of Technology. Center for Environmental Health Sciences | en_US |
dc.contributor.department | Massachusetts Institute of Technology. Department of Biology | en_US |
dc.relation.journal | Nature Communications | en_US |
dc.eprint.version | Final published version | en_US |
dc.type.uri | http://purl.org/eprint/type/JournalArticle | en_US |
eprint.status | http://purl.org/eprint/status/PeerReviewed | en_US |
dc.date.updated | 2020-01-23T13:39:05Z | |
dspace.date.submission | 2020-01-23T13:39:07Z | |
mit.journal.volume | 10 | en_US |
mit.metadata.status | Complete | |