Virus Control Goes Epigenetic

Summary

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Cells have developed a number of mechanisms to detect and suppress microbial infections. The use of pattern recognition receptors (PRRs) is one such mechanism. PRRs may be expressed on the cell surface, in the cytosol, or in the endosomes, to detect pathogen-associated molecular patterns (PAMPs) or the danger signals released by damaged cells (i.e., damage-associated molecular patterns; DAMPs). PRR activation triggers a signaling cascade, resulting in the production of antimicrobial cytokines, including type I interferons. These cytokines will in turn induce the expression of genes, such as interferon-stimulated genes (ISGs), that exhibit antimicrobial activities. In addition to PRRs, autophagy is another intracellular defense mechanism. Autophagy is used by the cells to remove intracellular pathogens in a process known as xenophagy [1]. Many viruses have developed different mechanisms to suppress these innate immune responses for their survival. A notable example is the cleavage of the mitochondrial antiviral signaling protein (MAVS) by the hepatitis C virus (HCV) NS3 protease [2]. MAVS is an important downstream adaptor molecule of RIG-I, which is a cytosolic PRR that can be activated by the HCV genomic RNA. Another example is the influenza virus NS1 protein, which binds to the E3 ubiquitin ligase TRIM25 to prevent it from activating RIG-I [3]. Similarly, the autophagy pathway may also be suppressed by viruses or even exploited by viruses to benefit their own replication. The former is typified by the herpes simplex virus-1 (HSV-1) ICP34.5 protein, which binds to Beclin-1 to prevent it from binding to and activating the class III phosphatidylinositol-3-kinase, an enzyme important for the initiation of autophagy. An example of the latter is HCV, which uses autophagy to enhance its replication [4].

In the report by Ducroux et al. [5], the authors presented yet another type of cellular control of viral infections. By using a tandem-affinity purification approach, the authors identified Spindlin1 as a binding partner of the hepatitis B virus (HBV) X protein (HBx). They subsequently discovered that Spindlin1 could suppress the replication of HBV, as its overexpression reduced the levels of HBV RNA and DNA replicative intermediates. On the contrary, depletion of Spindlin1 by RNA interference enhanced HBV replication. They then demonstrated that the suppressive effect of Spindlin1 on HBV was at the transcriptional level, as the overexpression of Spindlin1 reduced the transcriptional activity of HBV DNA by 80% in a nuclear run-on experiment. This effect of Spindlin1 on HBV was specific, as it was not observed with the cellular gene cyclin A2.

Spindlin1 contains three Tudor-like domains and can bind to trimethylated lysine 4 (H3K4me3) and asymmetric dimethylated arginine 8 (H3R8me2a) of histone H3 [6]. In the chromatin immunoprecipitation (ChIP) assay, Ducroux et al. demonstrated that Spindlin1 could bind to the HBV covalently closed circular DNA (cccDNA) genome. Interestingly, this binding was enhanced if the expression of HBx from the viral genome was abolished, suggesting an inhibitory role of HBx in the binding of Spindlin1 to the HBV genome. It does not appear likely that Spindlin1 binds to HBV cccDNA via H3K4me3, though, as the depletion of Spindlin1 actually led to a significant increase of the level of H3K4me3 in the HBV cccDNA. Their results suggested that Spindlin1, by binding to the HBV cccDNA, inhibits this post-translational modification of histone H3, which is associated with actively transcribed genes (Figure 1) [7].

A similar suppressive effect of Spindlin1 on the transcription of HSV-1 RNA was also observed by the authors. They found that the depletion of Spindlin1 also increased the ICP27 RNA level of HSV-1. In contrast, Spindlin1 had no effect on the replication of HCV, an RNA virus. Their results raise the possibility that Spindlin1, either by itself or by interacting with an unknown partner or partners, may represent a new class of PRRs that detect and suppress gene expression of DNA viruses by reducing the H3K4me3 level on the viral genome. If Spindlin1 is indeed a new PRR, then it will be interesting to determine how Spindlin1 differentiates episomal viral DNA from self DNA and what PAMPs it recognizes on the viral DNA. In their studies on HSV-1, Ducroux et al. did not demonstrate whether Spindlin1 could indeed reduce the H3K4me3 level associated with the HSV-1 genome, which must be demonstrated if the ability of Spindlin1 to exert epigenetic control on gene expression of DNA viruses is to be generalized. It will also be interesting in the future to determine whether Spindlin1 exhibits the same suppressive effect on other DNA viruses such as papillomaviruses and polyomaviruses and whether these DNA viruses also express gene products that can antagonize the suppressive effect of Spindlin1.