{"id":{"repo_id":"missouri","oai_identifier":"oai:mospace.umsystem.edu:10355/14379"},"canonical_url":"https://search.dev.ndltd.org/etd/missouri/oai:mospace.umsystem.edu:10355/14379","repository":{"repo_id":"missouri","name":"University of Missouri","base_url":"https://mospace.umsystem.edu/oai/request"},"display":{"title":"Establishment of a phenotypical model of adverse outcomes associated with assisted reproductive technologies","abstract":"Beckwith-Wiedemann syndrome (BWS) is a loss-of-imprinting pediatric overgrowth syndrome. BWS is speculated to occur primarily as the result of the misregulation of imprinted genes associated with two clusters on chromosome 11p15.5, namely the KvDMR1 and H19/IGF2. There is a similar overgrowth phenotype that is observed in ruminants as a result of embryo culture. This syndrome is known as large offspring syndrome (LOS). The genomic region/s associated with LOS have not yet been determined. We hypothesized that BWS and LOS are epigenetically similar. The aim of this research was to ascertain baseline allelic expression and DNA methylation in bovine of imprinted loci known to be misregulated in BWS. We conclude that the imprinted gene expression of KCNQ1OT1, CDKN1C, H19, and PLAGL1 are conserved between the bovine and human. In addition, the KvDMR1 and H19/IGF2 imprinting control regions also have conserved DNA methylation patterns between humans and bovine.","abstract_html":"Beckwith-Wiedemann syndrome (BWS) is a loss-of-imprinting pediatric overgrowth syndrome. BWS is speculated to occur primarily as the result of the misregulation of imprinted genes associated with two clusters on chromosome 11p15.5, namely the KvDMR1 and H19/IGF2. There is a similar overgrowth phenotype that is observed in ruminants as a result of embryo culture. This syndrome is known as large offspring syndrome (LOS). The genomic region/s associated with LOS have not yet been determined. We hypothesized that BWS and LOS are epigenetically similar. The aim of this research was to ascertain baseline allelic expression and DNA methylation in bovine of imprinted loci known to be misregulated in BWS. We conclude that the imprinted gene expression of KCNQ1OT1, CDKN1C, H19, and PLAGL1 are conserved between the bovine and human. In addition, the KvDMR1 and H19/IGF2 imprinting control regions also have conserved DNA methylation patterns between humans and bovine.","abstract_has_math":false,"creators":["Robbins, Katherine Marie"],"institution":"University of Missouri--Columbia","degree_name":"M.S.","degree_level":"Masters","degree_discipline":"Animal sciences (MU)","degree_department":null,"school":null,"contributors":[],"advisors":["Rivera, Rocío Melissa"],"committee_chairs":[],"committee_members":[],"year":2011,"date_issued":"2011","date_published":"2011","updated_at":"2026-07-24T03:07:13Z","subjects":["Beckwith-Wiedemann syndrome","epigenetics","genomic imprinting","methylation","large offspring syndrome"],"languages":["eng","English"],"rights":[],"rights_urls":[],"identifier_entries":[]},"links":{"outbound_url":"http://hdl.handle.net/10355/14379","outbound_label":"Handle","outbound_source":"dc:identifier.uri"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:contributor.advisor","label":"Advisor","values":["Rivera, Rocío Melissa"]},{"key":"dc:creator","label":"Author","values":["Robbins, Katherine Marie"]}]},{"id":"academic_context","label":"Academic Context","entries":[{"key":"dc:date.accessioned","label":"Dc Date Accessioned","values":["2012-05-24T19:57:37Z"]},{"key":"dc:date.available","label":"Dc Date Available","values":["2012-07-29T11:15:07Z"]},{"key":"dc:date.issued","label":"Date","values":["2011"]},{"key":"dc:publisher","label":"Institution","values":["University of Missouri--Columbia"]},{"key":"dc:type","label":"Dc Type","values":["Thesis"]},{"key":"thesis:degree_discipline","label":"Discipline","values":["Animal sciences (MU)"]},{"key":"thesis:degree_level","label":"Degree Level","values":["Masters"]},{"key":"thesis:degree_name","label":"Degree Name","values":["M.S."]},{"key":"thesis:institution_name","label":"Thesis Institution Name","values":["University of Missouri--Columbia"]}]},{"id":"subjects_keywords","label":"Subjects and Keywords","entries":[{"key":"dc:subject","label":"Dc Subject","values":["Beckwith-Wiedemann syndrome","epigenetics","genomic imprinting","methylation","large offspring syndrome"]}]},{"id":"language_rights","label":"Language and Rights","entries":[{"key":"dc:language","label":"Dc Language","values":["English"]},{"key":"dc:language.iso","label":"Language (ISO)","values":["eng"]}]},{"id":"identifiers","label":"Identifiers","entries":[{"key":"dc:identifier.uri","label":"Identifier URI","values":["http://hdl.handle.net/10355/14379"]}]},{"id":"additional","label":"Additional Metadata","entries":[{"key":"dc:description","label":"Description","values":["Title from PDF of title page (University of Missouri--Columbia, viewed on May 24, 2012).","The entire thesis text is included in the research.pdf file; the official abstract appears in the short.pdf file; a non-technical public abstract appears in the public.pdf file.","Thesis advisor: Dr. Rocío Melissa Rivera","Vita.","Includes bibliographical references.","Dissertations, Academic -- University of Missouri--Columbia -- Animal science.","\"July 2011\""]},{"key":"dc:description.abstract","label":"Abstract","values":["Beckwith-Wiedemann syndrome (BWS) is a loss-of-imprinting pediatric overgrowth syndrome. BWS is speculated to occur primarily as the result of the misregulation of imprinted genes associated with two clusters on chromosome 11p15.5, namely the KvDMR1 and H19/IGF2. There is a similar overgrowth phenotype that is observed in ruminants as a result of embryo culture. This syndrome is known as large offspring syndrome (LOS). The genomic region/s associated with LOS have not yet been determined. We hypothesized that BWS and LOS are epigenetically similar. The aim of this research was to ascertain baseline allelic expression and DNA methylation in bovine of imprinted loci known to be misregulated in BWS. We conclude that the imprinted gene expression of KCNQ1OT1, CDKN1C, H19, and PLAGL1 are conserved between the bovine and human. In addition, the KvDMR1 and H19/IGF2 imprinting control regions also have conserved DNA methylation patterns between humans and bovine."]},{"key":"dc:title","label":"Title","values":["Establishment of a phenotypical model of adverse outcomes associated with assisted reproductive technologies"]}]}],"canonical_facts":{"dc:contributor.advisor":["Rivera, Rocío Melissa"],"dc:creator":["Robbins, Katherine Marie"],"dc:date.accessioned":["2012-05-24T19:57:37Z"],"dc:date.available":["2012-07-29T11:15:07Z"],"dc:date.issued":["2011"],"dc:description":["Title from PDF of title page (University of Missouri--Columbia, viewed on May 24, 2012).","The entire thesis text is included in the research.pdf file; the official abstract appears in the short.pdf file; a non-technical public abstract appears in the public.pdf file.","Thesis advisor: Dr. Rocío Melissa Rivera","Vita.","Includes bibliographical references.","Dissertations, Academic -- University of Missouri--Columbia -- Animal science.","\"July 2011\""],"dc:description.abstract":["Beckwith-Wiedemann syndrome (BWS) is a loss-of-imprinting pediatric overgrowth syndrome. BWS is speculated to occur primarily as the result of the misregulation of imprinted genes associated with two clusters on chromosome 11p15.5, namely the KvDMR1 and H19/IGF2. There is a similar overgrowth phenotype that is observed in ruminants as a result of embryo culture. This syndrome is known as large offspring syndrome (LOS). The genomic region/s associated with LOS have not yet been determined. We hypothesized that BWS and LOS are epigenetically similar. The aim of this research was to ascertain baseline allelic expression and DNA methylation in bovine of imprinted loci known to be misregulated in BWS. We conclude that the imprinted gene expression of KCNQ1OT1, CDKN1C, H19, and PLAGL1 are conserved between the bovine and human. In addition, the KvDMR1 and H19/IGF2 imprinting control regions also have conserved DNA methylation patterns between humans and bovine."],"dc:identifier.uri":["http://hdl.handle.net/10355/14379"],"dc:language":["English"],"dc:language.iso":["eng"],"dc:publisher":["University of Missouri--Columbia"],"dc:subject":["Beckwith-Wiedemann syndrome","epigenetics","genomic imprinting","methylation","large offspring syndrome"],"dc:title":["Establishment of a phenotypical model of adverse outcomes associated with assisted reproductive technologies"],"dc:type":["Thesis"],"thesis:degree_discipline":["Animal sciences (MU)"],"thesis:degree_level":["Masters"],"thesis:degree_name":["M.S."],"thesis:institution_name":["University of Missouri--Columbia"]},"updated_at":"2026-07-24T03:07:13Z"}