Abstract

The discovery of the epigenetic regulation of gene expression has revolutionized both our understanding of how genomes function and approaches to the therapy of numerous pathologies. Schistosomes are metazoan parasites and as such utilize most, if not all the epigenetic mechanisms in play in their vertebrate hosts: histone variants, histone tail modifications, non-coding RNA and, perhaps, DNA methylation. Moreover, we are acquiring an increasing understanding of the ways in which these mechanisms come into play during the complex schistosome developmental program. In turn, interest in the actors involved in epigenetic mechanisms, particularly the enzymes that carry out epigenetic modifications of histones or nucleic acid, as therapeutic targets has been stimulated by the finding that their inhibitors exert profound effects, not only on survival, but also on the reproductive function of Schistosoma mansoni. Here, we review our current knowledge, and what we can infer, about the role of epigenetic mechanisms in schistosome development, differentiation and survival. We will consider which epigenetic actors can be targeted for drug discovery and what strategies can be employed to develop potent, selective inhibitors as drugs to cure schistosomiasis.

Highlights

  • Schistosomiasis is caused by flatworm parasites of the genus Schistosoma, five species of which infect humans in 74 tropical and sub-tropical countries

  • The precise mechanism of action of praziquantel in killing schistosomes is unknown, its initial effects include the rapid influx of Ca2+ ions and calcium-dependent muscle contraction and paralysis (Day et al, 1992) and this may be mediated via its interaction with a calcium channel beta subunit (Kohn et al, 2001)

  • This example proves the concept that individual epigenetic enzymes can be valid therapeutic targets, and that, even though www.frontiersin.org these enzymes generally have conserved catalytic domains, sufficient differences in structure can exist to allow the development of selective inhibitors that are drug precursors

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Summary

INTRODUCTION

Schistosomiasis is caused by flatworm parasites of the genus Schistosoma, five species of which infect humans in 74 tropical and sub-tropical countries. After both inhibitor treatment and RNAi to knock down transcripts of the HATs, the phenotypic effects on egg laying and development were correlated with decreased acetylation of H3 and H4, increased methylation at H3K27, a marker of transcriptional repression, on the p14 proximal promoter The effects of both HDAC and HAT inhibitors on schistosomes suggest that histone acetylation may be a legitimate therapeutic target and this was further supported by a preliminary study showing that HDAC inhibitors like TSA and valproic acid could induce time and dose-dependent death of schistosomes (adult worms or schistosomula larvae) in culture (Dubois et al, 2009). - These enzymes are evolutionarily conserved, their catalytic domains, and in order to avoid potential side effects, inhibitors that are selective for the schistosome enzyme have to be developed

Substrate specificity
Gene Ida
JmjC JmjC JmjC JmjC JmjC JmjC
CONCLUSIONS
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