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dc.contributor.authorRudgalvyte Martina
dc.contributor.authorPeltonen Juhani
dc.contributor.authorLakso Merja
dc.contributor.authorWong Garry
dc.date.accessioned2017-09-13T10:36:23Z
dc.date.available2017-09-13T10:36:23Z
dc.date.issued2017
dc.identifier.urihttps://erepo.uef.fi/handle/123456789/4277
dc.description.abstractMethylmercury (MeHg) is a persistent environmental pollutant that occurs in the food chain, at occupational sites, and via medical procedures. Exposure in humans and animal models results in renal, neuro, and reproductive toxicities. In this study, we demonstrate that chronic exposure to MeHg (10 μM) causes epigenetic landscape modifications of histone H3K4 trimethylation (H3K4me3) marks in Caenorhabditis elegans using chromatin immuno-precipitation sequencing (ChIP-seq). The modifications correspond to the locations of 1467 genes with enhanced and 508 genes with reduced signals. Among enhanced genes are those encoding glutathione-S-transferases, lipocalin-related protein and a cuticular collagen. ChIP-seq enhancement of these genes was confirmed with increased mRNA expression levels revealed by qRT-PCR. Furthermore, we observed enhancement of H3K4me3 marks in these genes in animals exposed to MeHg in utero and assayed at L4 stage. In utero exposure enhanced marks without alterations in mRNA expression except for the lpr-5 gene. Finally, knockdown of lipocalin-related protein gene lpr-5, which is involved in intercellular signaling, and cuticular collagen gene dpy-7, structural component of the cuticle, by RNA interference (RNAi) resulted in increased lethality of animals after MeHg exposure. Our results provide new data on the epigenetic landscape changes elicited by MeHg exposure, as well as describe a unique model for studying in utero effects of heavy metals. Together, these findings may help to understand the toxicological effects of MeHg at the molecular level.en
dc.language.isoENen
dc.publisherElsevier BVen
dc.relation.ispartofseriesComparative Biochemistry and Physiology. Part C. Toxicology & Pharmacologyen
dc.relation.urihttp://dx.doi.org/10.1016/j.cbpc.2016.10.001en
dc.rightsCC BY-NC-ND https://creativecommons.org/licenses/by-nc-nd/4.0/en
dc.subjectChromatin immunoprecipitation sequencingen
dc.subject(ChIP-seq)en
dc.subjectRNA sequencing (RNA-seq)en
dc.subjectHeavy metalen
dc.subjectEpigeneticsen
dc.subjectMercuryen
dc.titleChronic MeHg exposure modifies the histone H3K4me3 epigenetic landscape in Caenorhabditis elegansen
dc.description.versionpublished versionen
dc.contributor.departmentA.I. Virtanen -instituutti / Neurobiologiaen
uef.solecris.id45034773en
dc.type.publicationinfo:eu-repo/semantics/articleen
dc.rights.accessrights© Authorsen
dc.relation.doi10.1016/j.cbpc.2016.10.001en
dc.description.reviewstatuspeerRevieweden
dc.format.pagerange109-116en
dc.relation.issn1532-0456en
dc.relation.volume191en
dc.rights.accesslevelopenAccessen
dc.type.okmA1en
dc.type.versioninfo:eu-repo/semantics/publishedVersionen


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