Structural and functional studies of PCNA from African swine fever virus

Author:

Shao Zhiwei1,Yang Jie1,Gao Yanqing1,Zhang Yixi1,Zhao Xin1,Shao Qiyuan1,Zhang Weizhen1,Cao Chulei1,Liu Hehua1,Gan Jianhua1ORCID

Affiliation:

1. Shanghai Public Health Clinical Center, State Key Laboratory of Genetic Engineering, Collaborative Innovation Center of Genetics and Development, School of Life Sciences, Fudan University , Shanghai, China

Abstract

ABSTRACT Proliferating cell nuclear antigen (PCNA) belongs to the DNA sliding clamp family. Via interacting with various partner proteins, PCNA plays critical roles in DNA replication, DNA repair, chromatin assembly, epigenetic inheritance, chromatin remodeling, and many other fundamental biological processes. Although PCNA and PCNA-interacting partner networks are conserved across species, PCNA of a given species is rarely functional in heterologous systems, emphasizing the importance of more representative PCNA studies. Here, we report two crystal structures of PCNA from African swine fever virus (ASFV), which is the only member of the Asfarviridae family. Compared to the eukaryotic and archaeal PCNAs and the sliding clamp structural homologs from other viruses, Asfv PCNA possesses unique sequences and/or conformations at several regions, such as the J-loop, interdomain-connecting loop (IDCL), P-loop, and C-tail, which are involved in partner recognition or modification of sliding clamps. In addition to double-stranded DNA binding, we also demonstrate that Asfv PCNA can modestly enhance the ligation activity of the Asfv LIG protein. The unique structural features of Asfv PCNA can serve as a potential target for the development of ASFV-specific inhibitors and help combat the deadly virus. IMPORTANCE Two high-resolution crystal structures of African swine fever virus proliferating cell nuclear antigen ( Asfv PCNA) are presented here. Structural comparison revealed that Asfv PCNA is unique at several regions, such as the J-loop, the interdomain-connecting loop linker, and the P-loop, which may play important roles in ASFV-specific partner selection of Asfv PCNA. Unlike eukaryotic and archaeal PCNAs, Asfv PCNA possesses high double-stranded DNA-binding affinity. Besides DNA binding, Asfv PCNA can also modestly enhance the ligation activity of the Asfv LIG protein, which is essential for the replication and repair of ASFV genome. The unique structural features make Asfv PCNA a potential target for drug development, which will help combat the deadly virus.

Funder

MOST | National Natural Science Foundation of China

Publisher

American Society for Microbiology

Subject

Virology,Insect Science,Immunology,Microbiology

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