A widespread pathway for substitution of adenine by diaminopurine in phage genomes

Author:

Zhou Yan12ORCID,Xu Xuexia3456ORCID,Wei Yifeng7ORCID,Cheng Yu34ORCID,Guo Yu34,Khudyakov Ivan8ORCID,Liu Fuli9,He Ping9ORCID,Song Zhangyue10,Li Zhi1ORCID,Gao Yan1ORCID,Ang Ee Lui7ORCID,Zhao Huimin711ORCID,Zhang Yan12ORCID,Zhao Suwen34ORCID

Affiliation:

1. Tianjin Key Laboratory for Modern Drug Delivery and High-Efficiency, Collaborative Innovation Center of Chemical Science and Engineering, School of Pharmaceutical Science and Technology, Tianjin University, Tianjin 300072, China.

2. Frontiers Science Center for Synthetic Biology (Ministry of Education), Tianjin University, Tianjin 300072, China.

3. iHuman Institute, ShanghaiTech University, Shanghai 201210, China.

4. School of Life Science and Technology, ShanghaiTech University, Shanghai 201210, China.

5. University of Chinese Academy of Sciences, Beijing 100049, China.

6. Shanghai Institute of Nutrition and Health, Chinese Academy of Sciences, Shanghai 200061, China.

7. Singapore Institute of Food and Biotechnology Innovation, Agency for Science, Technology and Research (A*STAR), Singapore.

8. All-Russian Research Institute for Agricultural Microbiology, St. Petersburg 196608, Russia.

9. Department of Medical Microbiology and Immunology, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China.

10. Biomedical Big Data Platform, SIAIS, ShanghaiTech University, Shanghai 201210, China.

11. Department of Chemical and Biomolecular Engineering, University of Illinois at Urbana-Champaign, Urbana, IL 61801, USA.

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

National Natural Science Foundation of China

ShanghaiTech University

National Key Research and Development Program of China Stem Cell and Translational Research

National key R&D program of China

Zhang

Agency for Science Research and Technology of Singapore Visiting Investigator Program

Advanced Manufacturing and Engineering Programmatic

Agency for Science, Research and Technology of Singapore Visiting Investigator Program

A*STAR Advanced Manufacturing and Engineering Programmatic Grant

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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