{"title":"DNAJC9通过募集组蛋白H3.3结合并增强乙型肝炎病毒cccDNA转录","authors":"Tianhao Mao, Xinyu Du, Yukun Li, Zhao Zhou, Deyao Li, Liwei Zheng, Ting Zhang, Guixin Li, Danli Yang, Xiangmei Chen, Fengmin Lu","doi":"10.1002/jmv.70390","DOIUrl":null,"url":null,"abstract":"<div>\n \n <p>Hepatitis B virus (HBV) covalently closed circular DNA (cccDNA), the transcriptional template in HBV replication, is transcriptionally regulated by multiple host proteins such as epigenetic factors and transcription factors. This study aims to identify novel host proteins interacting with cccDNA and regulating its activity in HBV replication. Mass spectrometry analysis identified 129 host proteins associated with biotinylated cccDNA surrogate HBVcircle. A siRNA library screening demonstrated that knockdown of DNAJC9, CEBPZ, and EIF3A in HepG2 cells transfected with HBVcircle reduced the levels of HBsAg and HBeAg in the supernatant. Knockdown of DNAJC9 in HBV replication and infection cell models restricted viral replication, while the DNAJC9 overexpression showed an opposite trend. DNA pull-down, cccDNA ChIP, and immunofluorescence experiments indicated that DNAJC9 can bind to cccDNA in a manner independent of histones and specific DNA sequences. Dual luciferase reporter assay demonstrated that knockdown of DNAJC9 reduces the transcriptional activity of HBV promoters and enhancers. Co-IP and cccDNA ChIP experiments showed that DNAJC9 can interact with histone H3.3, and knockdown of DNAJC9 reduced H3.3, H3K4me3, and H3K27ac on cccDNA. In the HepAD38 or HepG2-NTCP cells, HBV replication led to a decrease in the cytoplasmic distribution and an increase in the nuclear distribution of DNAJC9. Histone chaperone DNAJC9 can bind to cccDNA in a histone-independent manner. DNAJC9 upregulates cccDNA transcription and viral replication by increasing the density of H3.3, H3K4me3, and H3K27ac on cccDNA, thereby activating its promoters and enhancers. HBV replication may promote the nuclear localization of DNAJC9 protein, thus facilitating active transcription and replication of HBV.</p></div>","PeriodicalId":16354,"journal":{"name":"Journal of Medical Virology","volume":"97 5","pages":""},"PeriodicalIF":6.8000,"publicationDate":"2025-05-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"DNAJC9 Binds to and Enhances the Transcription of Hepatitis B Virus cccDNA by Recruiting Histone H3.3\",\"authors\":\"Tianhao Mao, Xinyu Du, Yukun Li, Zhao Zhou, Deyao Li, Liwei Zheng, Ting Zhang, Guixin Li, Danli Yang, Xiangmei Chen, Fengmin Lu\",\"doi\":\"10.1002/jmv.70390\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div>\\n \\n <p>Hepatitis B virus (HBV) covalently closed circular DNA (cccDNA), the transcriptional template in HBV replication, is transcriptionally regulated by multiple host proteins such as epigenetic factors and transcription factors. This study aims to identify novel host proteins interacting with cccDNA and regulating its activity in HBV replication. Mass spectrometry analysis identified 129 host proteins associated with biotinylated cccDNA surrogate HBVcircle. A siRNA library screening demonstrated that knockdown of DNAJC9, CEBPZ, and EIF3A in HepG2 cells transfected with HBVcircle reduced the levels of HBsAg and HBeAg in the supernatant. Knockdown of DNAJC9 in HBV replication and infection cell models restricted viral replication, while the DNAJC9 overexpression showed an opposite trend. DNA pull-down, cccDNA ChIP, and immunofluorescence experiments indicated that DNAJC9 can bind to cccDNA in a manner independent of histones and specific DNA sequences. Dual luciferase reporter assay demonstrated that knockdown of DNAJC9 reduces the transcriptional activity of HBV promoters and enhancers. Co-IP and cccDNA ChIP experiments showed that DNAJC9 can interact with histone H3.3, and knockdown of DNAJC9 reduced H3.3, H3K4me3, and H3K27ac on cccDNA. In the HepAD38 or HepG2-NTCP cells, HBV replication led to a decrease in the cytoplasmic distribution and an increase in the nuclear distribution of DNAJC9. Histone chaperone DNAJC9 can bind to cccDNA in a histone-independent manner. DNAJC9 upregulates cccDNA transcription and viral replication by increasing the density of H3.3, H3K4me3, and H3K27ac on cccDNA, thereby activating its promoters and enhancers. HBV replication may promote the nuclear localization of DNAJC9 protein, thus facilitating active transcription and replication of HBV.</p></div>\",\"PeriodicalId\":16354,\"journal\":{\"name\":\"Journal of Medical Virology\",\"volume\":\"97 5\",\"pages\":\"\"},\"PeriodicalIF\":6.8000,\"publicationDate\":\"2025-05-23\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Medical Virology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/jmv.70390\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"VIROLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Medical Virology","FirstCategoryId":"3","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/jmv.70390","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"VIROLOGY","Score":null,"Total":0}
DNAJC9 Binds to and Enhances the Transcription of Hepatitis B Virus cccDNA by Recruiting Histone H3.3
Hepatitis B virus (HBV) covalently closed circular DNA (cccDNA), the transcriptional template in HBV replication, is transcriptionally regulated by multiple host proteins such as epigenetic factors and transcription factors. This study aims to identify novel host proteins interacting with cccDNA and regulating its activity in HBV replication. Mass spectrometry analysis identified 129 host proteins associated with biotinylated cccDNA surrogate HBVcircle. A siRNA library screening demonstrated that knockdown of DNAJC9, CEBPZ, and EIF3A in HepG2 cells transfected with HBVcircle reduced the levels of HBsAg and HBeAg in the supernatant. Knockdown of DNAJC9 in HBV replication and infection cell models restricted viral replication, while the DNAJC9 overexpression showed an opposite trend. DNA pull-down, cccDNA ChIP, and immunofluorescence experiments indicated that DNAJC9 can bind to cccDNA in a manner independent of histones and specific DNA sequences. Dual luciferase reporter assay demonstrated that knockdown of DNAJC9 reduces the transcriptional activity of HBV promoters and enhancers. Co-IP and cccDNA ChIP experiments showed that DNAJC9 can interact with histone H3.3, and knockdown of DNAJC9 reduced H3.3, H3K4me3, and H3K27ac on cccDNA. In the HepAD38 or HepG2-NTCP cells, HBV replication led to a decrease in the cytoplasmic distribution and an increase in the nuclear distribution of DNAJC9. Histone chaperone DNAJC9 can bind to cccDNA in a histone-independent manner. DNAJC9 upregulates cccDNA transcription and viral replication by increasing the density of H3.3, H3K4me3, and H3K27ac on cccDNA, thereby activating its promoters and enhancers. HBV replication may promote the nuclear localization of DNAJC9 protein, thus facilitating active transcription and replication of HBV.
期刊介绍:
The Journal of Medical Virology focuses on publishing original scientific papers on both basic and applied research related to viruses that affect humans. The journal publishes reports covering a wide range of topics, including the characterization, diagnosis, epidemiology, immunology, and pathogenesis of human virus infections. It also includes studies on virus morphology, genetics, replication, and interactions with host cells.
The intended readership of the journal includes virologists, microbiologists, immunologists, infectious disease specialists, diagnostic laboratory technologists, epidemiologists, hematologists, and cell biologists.
The Journal of Medical Virology is indexed and abstracted in various databases, including Abstracts in Anthropology (Sage), CABI, AgBiotech News & Information, National Agricultural Library, Biological Abstracts, Embase, Global Health, Web of Science, Veterinary Bulletin, and others.