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Tissue- specific DNA methylation profiles in newborns

dc.contributor.advisorSteegers - Theunissen, Regine
dc.creatorGalvez Bermudez, Jubby Marcela
dc.creator.degreeMagíster en Ciencias con Énfasis en Genética Humana
dc.date.accessioned2013-01-30T17:53:45Z
dc.date.available2013-01-30T17:53:45Z
dc.date.created2011-09-02
dc.date.issued2011
dc.description.abstractExperimental and epidemiological studies demonstrate that fetal growth restriction and low birth weight enhance the risk of chronic diseases in adulthood. Derangements in tissue-specific epigenetic programming of fetal and placental tissues are a suggested mechanism of which DNA methylation is best understood. DNA methylation profiles in human tissue are mostly performed in DNA from white blood cells. The objective of this study was to assess DNA methylation profiles of IGF2 DMR and H19 in DNA derived from four tissues of the newborn. We obtained from 6 newborns DNA from fetal placental tissue (n = 5), umbilical cord CD34+ hematopoietic stem cells (HSC) and CD34- mononuclear cells (MNC) (n = 6), and umbilical cord Wharton jelly (n = 5). HCS were isolated using magnetic-activated cell separation. DNA methylation of the imprinted fetal growth genes IGF2 DMR and H19 was measured in all tissues using quantitative mass spectrometry. ANOVA testing showed tissue-specific differences in DNA methylation of IGF2 DMR (p value 0.002) and H19 (p value 0.001) mainly due to a higher methylation of IGF2 DMR in Wharton jelly (mean 0.65, sd 0.14) and a lower methylation of H19 in placental tissue (mean 0.25, sd 0.02) compared to other tissues. This study demonstrates the feasibility of the assessment of differential tissue specific DNA methylation. Although the results have to be confirmed in larger sample sizes, our approach gives opportunities to investigate epigenetic profiles as underlying mechanism of associations between pregnancy exposures and outcome, and disease risks in later life.eng
dc.description.sponsorshipErasmus MC, University Medical Center Rotterdam, The Netherlandsspa
dc.format.mimetypeapplication/pdf
dc.format.tipoDocumentospa
dc.identifier.doihttps://doi.org/10.48713/10336_4138
dc.identifier.urihttp://repository.urosario.edu.co/handle/10336/4138
dc.language.isospa
dc.publisherUniversidad del Rosariospa
dc.publisher.departmentFacultad de medicinaspa
dc.publisher.programMaestría en Ciencias con Énfasis en Genética Humanaspa
dc.rights.accesRightsinfo:eu-repo/semantics/closedAccess
dc.rights.accesoBloqueado (Texto referencial)spa
dc.rights.ccAtribución-NoComercial-SinDerivadas 2.5 Colombiaspa
dc.rights.licenciaEL AUTOR, manifiesta que la obra objeto de la presente autorización es original y la realizó sin violar o usurpar derechos de autor de terceros, por lo tanto la obra es de exclusiva autoría y tiene la titularidad sobre la misma. PARÁGRAFO: En caso de presentarse cualquier reclamación o acción por parte de un tercero en cuanto a los derechos de autor sobre la obra en cuestión, EL AUTOR, asumirá toda la responsabilidad, y saldrá en defensa de los derechos aquí autorizados; para todos los efectos la universidad actúa como un tercero de buena fe. EL AUTOR, autoriza a LA UNIVERSIDAD DEL ROSARIO, para que en los términos establecidos en la Ley 23 de 1982, Ley 44 de 1993, Decisión andina 351 de 1993, Decreto 460 de 1995 y demás normas generales sobre la materia, utilice y use la obra objeto de la presente autorización.spa
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/2.5/co/
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dc.source.instnameinstname:Universidad del Rosariospa
dc.source.reponamereponame:Repositorio Institucional EdocURspa
dc.subjectEpigenomicsspa
dc.subjectUmbilical cordspa
dc.subjecthematopoietic stem cellspa
dc.subjectWharton jellyspa
dc.subjectPlacentaspa
dc.subjectImprintingspa
dc.subjectIGF2spa
dc.subjectH19spa
dc.subject.keywordEpigenomicseng
dc.subject.keywordUmbilical cordeng
dc.subject.keywordHematopoietic stem celleng
dc.subject.keywordLeukocyteseng
dc.subject.keywordWharton jellyeng
dc.subject.keywordPlacentaeng
dc.subject.keywordImprintingeng
dc.subject.keywordIGF2eng
dc.subject.keywordH19eng
dc.subject.lembComplicaciones del embarazo::Aspectos Genéticosspa
dc.subject.lembEnfermedades crónicasspa
dc.subject.lembEnfermedades genéticas en el embarazospa
dc.subject.lembMetilación de adnspa
dc.titleTissue- specific DNA methylation profiles in newbornsspa
dc.typemasterThesiseng
dc.type.hasVersioninfo:eu-repo/semantics/acceptedVersion
dc.type.spaTesis de maestríaspa
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