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Exploring m6A and m5C Epitranscriptomes upon Viral Infection: an Example with HIV
Published on: March 5, 2022
Viral epigenetics
Barry I Milavetz1, Lata Balakrishnan
1Department of Basic Sciences, School of Medicine and Health Sciences, University of North Dakota, Stop 9037, 501 N. Columbia Rd., Grand Forks, ND, 58202, USA, barry.milavetz@med.und.edu.
Abstract:
DNA tumor viruses including members of the polyomavirus, adenovirus, papillomavirus, and herpes virus families are presently the subject of intense interest with respect to the role that epigenetics plays in control of the virus life cycle and the transformation of a normal cell to a cancer cell. To date, these studies have primarily focused on the role of histone modification, nucleosome location, and DNA methylation in regulating the biological consequences of infection. Using a wide variety of strategies and techniques ranging from simple ChIP to ChIP-chip and ChIP-seq to identify histone modifications, nuclease digestion to genome wide next generation sequencing to identify nucleosome location, and bisulfite treatment to MeDIP to identify DNA methylation sites, the epigenetic regulation of these viruses is slowly becoming better understood. While the viruses may differ in significant ways from each other and cellular chromatin, the role of epigenetics appears to be relatively similar. Within the viral genome nucleosomes are organized for the expression of appropriate genes with relevant histone modifications particularly histone acetylation. DNA methylation occurs as part of the typical gene silencing during latent infection by herpesviruses. In the simple tumor viruses like the polyomaviruses, adenoviruses, and papillomaviruses, transformation of the cell occurs via integration of the virus genome such that the virus's normal regulation is disrupted. This results in the unregulated expression of critical viral genes capable of redirecting cellular gene expression. The redirected cellular expression is a consequence of either indirect epigenetic regulation where cellular signaling or transcriptional dysregulation occurs or direct epigenetic regulation where epigenetic cofactors such as histone deacetylases are targeted. In the more complex herpersviruses transformation is a consequence of the expression of the viral latency proteins and RNAs which again can have either a direct or indirect effect on epigenetic regulation of cellular expression. Nevertheless, many questions still remain with respect to the specific mechanisms underlying epigenetic regulation of the viruses and transformation.
Insights
Epigenetics, including histone modification and DNA methylation, plays a key role in DNA tumor virus life cycles and cancer cell transformation. Understanding these epigenetic mechanisms is crucial for viral infection and cancer research.
Area of Science:
- Virology
- Epigenetics
- Oncology
Background:
- DNA tumor viruses (polyomavirus, adenovirus, papillomavirus, herpesvirus) are linked to cancer.
- Epigenetic mechanisms like histone modification, nucleosome location, and DNA methylation regulate viral life cycles and cellular transformation.
- Current research focuses on understanding the role of epigenetics in viral oncogenesis.
Purpose of the Study:
- To explore the role of epigenetics in the life cycle and cancer-causing potential of DNA tumor viruses.
- To elucidate how epigenetic modifications influence viral gene expression and cellular transformation.
- To highlight the common and distinct epigenetic regulatory strategies employed by different DNA tumor viruses.
Main Methods:
- Chromatin immunoprecipitation (ChIP), ChIP-chip, and ChIP-seq for histone modifications.
- Nuclease digestion and next-generation sequencing for nucleosome location.
- Bisulfite sequencing and methylated DNA immunoprecipitation (MeDIP) for DNA methylation analysis.
Main Results:
- Epigenetic regulation, particularly histone acetylation, is crucial for viral gene expression.
- DNA methylation is involved in gene silencing during latent herpesvirus infections.
- Viral genome integration in simple tumor viruses disrupts normal regulation, leading to uncontrolled viral gene expression and cellular transformation.
- Latency proteins and RNAs in herpesviruses also influence cellular epigenetic regulation.
Conclusions:
- Epigenetics is a fundamental mechanism controlling DNA tumor virus behavior and oncogenesis.
- Despite viral differences, epigenetic roles in gene expression and transformation are broadly conserved.
- Further research is needed to fully understand the specific epigenetic mechanisms driving viral oncogenesis.
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