Noncanonical DNA polymerization by aminoadenine-based siphoviruses

Author:

Pezo Valerie1ORCID,Jaziri Faten1,Bourguignon Pierre-Yves23ORCID,Louis Dominique4,Jacobs-Sera Deborah5ORCID,Rozenski Jef6ORCID,Pochet Sylvie7ORCID,Herdewijn Piet6ORCID,Hatfull Graham F.5ORCID,Kaminski Pierre-Alexandre8ORCID,Marliere Philippe13ORCID

Affiliation:

1. Génomique Métabolique, Genoscope, Institut François Jacob, CEA, CNRS, Univ. Evry, Université Paris-Saclay, 2 Rue Gaston Crémieux, 91057 Evry, France.

2. Werkstatt fuer Potenzielle Genetik, Naunynstrasse 30, 10997 Berlin, Germany.

3. TESSSI, 81 Rue Réaumur, 75002 Paris, France.

4. Alderys, 86 Rue de Paris, 91400 Orsay, France.

5. Department of Biological Sciences, University of Pittsburgh, 4249 Fifth Avenue, Pittsburgh, PA 15260 USA.

6. Laboratory of Medicinal Chemistry, Rega Institute for Biomedical Research, KU Leuven, Herestraat 49, Box 1041, 3000 Leuven, Belgium.

7. Organic Chemistry, CNRS UMR3523, Department of Chemistry and Biocatalysis, Institut Pasteur, 25-28 Rue du Docteur Roux, 75015 Paris, France.

8. Biology of Gram-Positive Pathogens, CNRS URL3526, Department of Microbiology, Institut Pasteur, 25-28 Rue du Docteur Roux, 75015 Paris, France.

Abstract

Biosynthesis and replication, from A to Z Four nucleobases. adenine (A), cytosine (C), guanine (G), and thymine (T), are usually thought to be invariable in DNA. In bacterial viruses, however, each of the DNA bases have variations that help them to escape degradation by bacterial restriction enzymes. In the genome of cyanophage S-2L, A is completely replaced by diaminopurine (Z), which forms three hydrogen bonds with T and thus creates non–Watson-Crick base pairing in the DNA of this virus (see the Perspective by Grome and Isaacs). Zhou et al. and Sleiman et al. determined the biochemical pathway that produces Z, which revealed more Z genomes in viruses hosted in bacteria distributed widely in the environment and phylogeny. Pezo et al. identified a DNA polymerase that incorporates Z into DNA while rejecting A. These findings enrich our understanding of biodiversity and expand the genetic palette for synthetic biology. Science , this issue p. 512 , 516 , 520 ; see also p. 460

Funder

European Research Council

ERASynBio

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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