Master mitotic kinases regulate viral genome delivery during papillomavirus cell entry

Author:

Rizzato MatteoORCID,Mao FuxiangORCID,Chardon Florian,Lai Kun-Yi,Villalonga-Planells RuthORCID,Drexler Hannes C. A.ORCID,Pesenti Marion E.ORCID,Fiskin Mert,Roos Nora,King Kelly M.,Li Shuaizhi,Gamez Eduardo R.,Greune Lilo,Dersch Petra,Simon ClaudiaORCID,Masson MurielleORCID,Van Doorslaer KoenraadORCID,Campos Samuel K.,Schelhaas MarioORCID

Abstract

AbstractMitosis induces cellular rearrangements like spindle formation, Golgi fragmentation, and nuclear envelope breakdown. Similar to certain retroviruses, nuclear delivery during entry of human papillomavirus (HPV) genomes is facilitated by mitosis, during which minor capsid protein L2 tethers viral DNA to mitotic chromosomes. However, the mechanism of viral genome delivery and tethering to condensed chromosomes is barely understood. It is unclear, which cellular proteins facilitate this process or how this process is regulated. This work identifies crucial phosphorylations on HPV minor capsid protein L2 occurring at mitosis onset. L2’s chromosome binding region (CBR) is sequentially phosphorylated by the master mitotic kinases CDK1 and PLK1. L2 phosphorylation, thus, regulates timely delivery of HPV vDNA to mitotic chromatin during mitosis. In summary, our work demonstrates a crucial role of mitotic kinases for nuclear delivery of viral DNA and provides important insights into the molecular mechanism of pathogen import into the nucleus during mitosis.

Publisher

Springer Science and Business Media LLC

Subject

General Physics and Astronomy,General Biochemistry, Genetics and Molecular Biology,General Chemistry,Multidisciplinary

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