Molecular Mechanism of the Cytosine CRISPR Base Editing Process and the Roles of Translesion DNA Polymerases-Reference-Cited by-同舟云学术

Molecular Mechanism of the Cytosine CRISPR Base Editing Process and the Roles of Translesion DNA Polymerases

Published:2021-12-01 Issue:12 Volume:10 Page:3353-3358
ISSN:2161-5063
Container-title:ACS Synthetic Biology
language:en
Short-container-title:ACS Synth. Biol.

Author:

Jiang Guo¹²,Wang Jie²³,Zhao Dongdong²,Chen Xuxu¹⁴⁵,Pu Shiming¹,Zhang Chunzhi³,Li Ju⁶,Li Yaqiu²⁷⁸,Yang Jie²⁷⁸,Li Siwei²⁷⁸,Liao Xiaoping²⁷⁸,Ma Hongwu²⁷⁸,Ma Yanhe²⁸,Zhou Zuping¹,Bi Changhao²⁷⁸^ORCID,Zhang Xueli²⁷⁸^ORCID

Affiliation:

1. College of Life Science, Guangxi Normal University, Guilin 541004, China

2. Tianjin Institute of Industrial Biotechnology, Chinese Academy of Sciences, Tianjin 300308, China

3. School of Biological Engineering, Dalian Polytechnic University, Dalian 116034, China

4. Guangxi Universities Key Laboratory of Stem Cell and Biopharmaceutical Technology, Guangxi Normal University, Guilin 541004, China

5. Research Center for Biomedical Sciences, Guangxi Normal University, Guilin 541004, China

6. College of Life Science, Tianjin Normal University, Tianjin 300387, China

7. Key Laboratory of Systems Microbial Biotechnology, Chinese Academy of Sciences, Tianjin 300308, China

8. National Technology Innovation Center of Synthetic Biology, Tianjin 300308, China

Funder

Ministry of Science and Technology of the People's Republic of China

National Natural Science Foundation of China

Chinese Academy of Sciences

Tianjin Synthetic Biotechnology Innovation Capacity Improvement Project

Publisher

American Chemical Society (ACS)

Subject

Biochemistry, Genetics and Molecular Biology (miscellaneous),Biomedical Engineering,General Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/acssynbio.1c00293

Reference20 articles.

1. Programmable editing of a target base in genomic DNA without double-stranded DNA cleavage

2. Targeted nucleotide editing using hybrid prokaryotic and vertebrate adaptive immune systems

3. Programmable base editing of A•T to G•C in genomic DNA without DNA cleavage

4. Deaminase-mediated multiplex genome editing in Escherichia coli

5. Double-Check Base Editing for Efficient A to G Conversions

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