BZLF1 governs CpG-methylated chromatin of Epstein-Barr Virus reversing epigenetic repression.
Epigenetic mechanisms are essential for the regulation of all genes in mammalian cells but transcriptional repression including DNA methylation are also major epigenetic mechanisms of defense inactivating potentially harmful pathogens. Epstein-Barr Virus (EBV), however, has evolved to take advantage...
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| Format: | Article |
| Language: | English |
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Public Library of Science (PLoS)
2012-09-01
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| Series: | PLoS Pathogens |
| Online Access: | http://europepmc.org/articles/PMC3435241?pdf=render |
| _version_ | 1811327593800007680 |
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| author | Anne Woellmer Jose M Arteaga-Salas Wolfgang Hammerschmidt |
| author_facet | Anne Woellmer Jose M Arteaga-Salas Wolfgang Hammerschmidt |
| author_sort | Anne Woellmer |
| collection | DOAJ |
| description | Epigenetic mechanisms are essential for the regulation of all genes in mammalian cells but transcriptional repression including DNA methylation are also major epigenetic mechanisms of defense inactivating potentially harmful pathogens. Epstein-Barr Virus (EBV), however, has evolved to take advantage of CpG methylated DNA to regulate its own biphasic life cycle. We show here that latent EBV DNA has an extreme composition of methylated CpG dinucleotides with a bimodal distribution of unmethylated or fully methylated DNA at active latent genes or completely repressed lytic promoters, respectively. We find this scenario confirmed in primary EBV-infected memory B cells in vivo. Extensive CpG methylation of EBV's DNA argues for a very restricted gene expression during latency. Above-average nucleosomal occupancy, repressive histone marks, and Polycomb-mediated epigenetic silencing further shield early lytic promoters from activation during latency. The very tight repression of viral lytic genes must be overcome when latent EBV enters its lytic phase and supports de novo virus synthesis in infected cells. The EBV-encoded and AP-1 related transcription factor BZLF1 overturns latency and initiates virus synthesis in latently infected cells. Paradoxically, BZLF1 preferentially binds to CpG-methylated motifs in key viral promoters for their activation. Upon BZLF1 binding, we find nucleosomes removed, Polycomb repression lost, and RNA polymerase II recruited to the activated early promoters promoting efficient lytic viral gene expression. Surprisingly, DNA methylation is maintained throughout this phase of viral reactivation and is no hindrance to active transcription of extensively CpG methylated viral genes as thought previously. Thus, we identify BZLF1 as a pioneer factor that reverses epigenetic silencing of viral DNA to allow escape from latency and report on a new paradigm of gene regulation. |
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| institution | Directory Open Access Journal |
| issn | 1553-7366 1553-7374 |
| language | English |
| last_indexed | 2024-04-13T15:09:32Z |
| publishDate | 2012-09-01 |
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| series | PLoS Pathogens |
| spelling | doaj.art-fd225b0cae2d41c6a75a085a851ec14b2022-12-22T02:42:03ZengPublic Library of Science (PLoS)PLoS Pathogens1553-73661553-73742012-09-0189e100290210.1371/journal.ppat.1002902BZLF1 governs CpG-methylated chromatin of Epstein-Barr Virus reversing epigenetic repression.Anne WoellmerJose M Arteaga-SalasWolfgang HammerschmidtEpigenetic mechanisms are essential for the regulation of all genes in mammalian cells but transcriptional repression including DNA methylation are also major epigenetic mechanisms of defense inactivating potentially harmful pathogens. Epstein-Barr Virus (EBV), however, has evolved to take advantage of CpG methylated DNA to regulate its own biphasic life cycle. We show here that latent EBV DNA has an extreme composition of methylated CpG dinucleotides with a bimodal distribution of unmethylated or fully methylated DNA at active latent genes or completely repressed lytic promoters, respectively. We find this scenario confirmed in primary EBV-infected memory B cells in vivo. Extensive CpG methylation of EBV's DNA argues for a very restricted gene expression during latency. Above-average nucleosomal occupancy, repressive histone marks, and Polycomb-mediated epigenetic silencing further shield early lytic promoters from activation during latency. The very tight repression of viral lytic genes must be overcome when latent EBV enters its lytic phase and supports de novo virus synthesis in infected cells. The EBV-encoded and AP-1 related transcription factor BZLF1 overturns latency and initiates virus synthesis in latently infected cells. Paradoxically, BZLF1 preferentially binds to CpG-methylated motifs in key viral promoters for their activation. Upon BZLF1 binding, we find nucleosomes removed, Polycomb repression lost, and RNA polymerase II recruited to the activated early promoters promoting efficient lytic viral gene expression. Surprisingly, DNA methylation is maintained throughout this phase of viral reactivation and is no hindrance to active transcription of extensively CpG methylated viral genes as thought previously. Thus, we identify BZLF1 as a pioneer factor that reverses epigenetic silencing of viral DNA to allow escape from latency and report on a new paradigm of gene regulation.http://europepmc.org/articles/PMC3435241?pdf=render |
| spellingShingle | Anne Woellmer Jose M Arteaga-Salas Wolfgang Hammerschmidt BZLF1 governs CpG-methylated chromatin of Epstein-Barr Virus reversing epigenetic repression. PLoS Pathogens |
| title | BZLF1 governs CpG-methylated chromatin of Epstein-Barr Virus reversing epigenetic repression. |
| title_full | BZLF1 governs CpG-methylated chromatin of Epstein-Barr Virus reversing epigenetic repression. |
| title_fullStr | BZLF1 governs CpG-methylated chromatin of Epstein-Barr Virus reversing epigenetic repression. |
| title_full_unstemmed | BZLF1 governs CpG-methylated chromatin of Epstein-Barr Virus reversing epigenetic repression. |
| title_short | BZLF1 governs CpG-methylated chromatin of Epstein-Barr Virus reversing epigenetic repression. |
| title_sort | bzlf1 governs cpg methylated chromatin of epstein barr virus reversing epigenetic repression |
| url | http://europepmc.org/articles/PMC3435241?pdf=render |
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