A Study of Alterations in DNA Epigenetic Modifications (5mC and 5hmC) and Gene Expression Influenced by Simulated Microgravity in Human Lymphoblastoid Cells

dc.contributor.author Chowdhury, Basudev
dc.contributor.author Seetharam, Arun
dc.contributor.author Wang, Zhiping
dc.contributor.author Liu, Yunlong
dc.contributor.author Lossie, Amy
dc.contributor.author Thimmapuram, Jyothi
dc.contributor.author Irudayaraj, Joseph
dc.contributor.department Genome Informatics Facility
dc.date 2018-04-13T21:35:32.000
dc.date.accessioned 2020-06-30T04:05:18Z
dc.date.available 2020-06-30T04:05:18Z
dc.date.copyright Fri Jan 01 00:00:00 UTC 2016
dc.date.issued 2016-01-28
dc.description.abstract <p>Cells alter their gene expression in response to exposure to various environmental changes. Epigenetic mechanisms such as DNA methylation are believed to regulate the alterations in gene expression patterns. <em>In vitro</em> and <em>in vivo</em> studies have documented changes in cellular proliferation, cytoskeletal remodeling, signal transduction, bone mineralization and immune deficiency under the influence of microgravity conditions experienced in space. However microgravity induced changes in the epigenome have not been well characterized. In this study we have used Next-generation Sequencing (NGS) to profile ground-based “simulated” microgravity induced changes on DNA methylation (5-methylcytosine or 5mC), hydroxymethylation (5-hydroxymethylcytosine or 5hmC), and simultaneous gene expression in cultured human lymphoblastoid cells. Our results indicate that simulated microgravity induced alterations in the methylome (~60% of the differentially methylated regions or DMRs are hypomethylated and ~92% of the differentially hydroxymethylated regions or DHMRs are hyperhydroxymethylated). Simulated microgravity also induced differential expression in 370 transcripts that were associated with crucial biological processes such as oxidative stress response, carbohydrate metabolism and regulation of transcription. While we were not able to obtain any global trend correlating the changes of methylation/ hydroxylation with gene expression, we have been able to profile the simulated microgravity induced changes of 5mC over some of the differentially expressed genes that includes five genes undergoing differential methylation over their promoters and twenty five genes undergoing differential methylation over their gene-bodies. To the best of our knowledge, this is the first NGS-based study to profile epigenomic patterns induced by short time exposure of simulated microgravity and we believe that our findings can be a valuable resource for future explorations.</p>
dc.description.comments <p>This article is published as Chowdhury B, Seetharam A, Wang Z, Liu Y, Lossie AC, Thimmapuram J, et al. (2016) A Study of Alterations in DNA Epigenetic Modifications (5mC and 5hmC) and Gene Expression Influenced by Simulated Microgravity in Human Lymphoblastoid Cells. <em>PLoS ONE</em> 11(1): e0147514. doi: <a href="http://dx.doi.org/10.1371/%20journal.pone.0147514" target="_blank">10.1371/ journal.pone.0147514</a>. Posted with permission.</p>
dc.format.mimetype application/pdf
dc.identifier archive/lib.dr.iastate.edu/genomeinformatics_pubs/4/
dc.identifier.articleid 1004
dc.identifier.contextkey 11961167
dc.identifier.s3bucket isulib-bepress-aws-west
dc.identifier.submissionpath genomeinformatics_pubs/4
dc.identifier.uri https://dr.lib.iastate.edu/handle/20.500.12876/38331
dc.language.iso en
dc.source.bitstream archive/lib.dr.iastate.edu/genomeinformatics_pubs/4/2016_Seetharam_StudyAlterations.PDF|||Sat Jan 15 00:04:07 UTC 2022
dc.source.uri 10.1371/journal.pone.0147514
dc.subject.disciplines Bioinformatics
dc.subject.disciplines Genetics
dc.subject.disciplines Genomics
dc.title A Study of Alterations in DNA Epigenetic Modifications (5mC and 5hmC) and Gene Expression Influenced by Simulated Microgravity in Human Lymphoblastoid Cells
dc.type article
dc.type.genre article
dspace.entity.type Publication
relation.isAuthorOfPublication e2191023-2773-4daf-8d00-0f57cd714bc1
relation.isOrgUnitOfPublication a408457b-982c-4070-a227-0aa9592ac0b5
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