Epigenomic Landscapes of hESC-Derived Neural Rosettes: Modeling Neural Tube Formation and Diseases

dc.contributor.authorCristina Valensisi
dc.contributor.authorColin Andrus
dc.contributor.authorSam Buckberry
dc.contributor.authorNaresh Doni Jayavelu
dc.contributor.authorRiikka Lund
dc.contributor.authorRyan Lister
dc.contributor.authorDavid Hawkins
dc.contributor.organizationfi=Turun biotiedekeskus|en=Turku Bioscience Centre|
dc.contributor.organization-code1.2.246.10.2458963.20.18586209670
dc.contributor.organization-code2609200
dc.contributor.organization-code2609201
dc.contributor.organization-code2609210
dc.converis.publication-id24980552
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/24980552
dc.date.accessioned2022-10-28T12:39:14Z
dc.date.available2022-10-28T12:39:14Z
dc.description.abstract<p>We currently lack a comprehensive understanding of the mechanisms underlying neural tube formation and their contributions to neural tube defects (NTDs). Developing a model to study such a complex morphogenetic process, especially one that models human-specific aspects, is critical. Three-dimensional, human embryonic stem cell (hESC)-derived neural rosettes (NRs) provide a powerful resource for in vitro modeling of human neural tube formation. Epigenomic maps reveal enhancer elements unique to NRs relative to 2D systems. A master regulatory network illustrates that key NR properties are related to their epigenomic landscapes. We found that folate-associated DNA methylation changes were enriched within NR regulatory elements near genes involved in neural tube formation and metabolism. Our comprehensive regulatory maps offer insights into the mechanisms by which folate may prevent NTDs. Lastly, our distal regulatory maps provide a better understanding of the potential role of neurological-disorder-associated SNPs.</p>
dc.format.pagerange1448
dc.format.pagerange1462
dc.identifier.jour-issn2211-1247
dc.identifier.olddbid177989
dc.identifier.oldhandle10024/161083
dc.identifier.urihttps://www.utupub.fi/handle/11111/35267
dc.identifier.urlhttps://doi.org/10.1016/j.celrep.2017.07.036
dc.identifier.urnURN:NBN:fi-fe2021042716958
dc.language.isoen
dc.okm.affiliatedauthorValensisi, Cristina
dc.okm.affiliatedauthorDoni Jayavelu, Naresh
dc.okm.affiliatedauthorLund, Riikka
dc.okm.affiliatedauthorHawkins, David
dc.okm.discipline1182 Biochemistry, cell and molecular biologyen_GB
dc.okm.discipline1184 Genetics, developmental biology, physiologyen_GB
dc.okm.discipline1182 Biokemia, solu- ja molekyylibiologiafi_FI
dc.okm.discipline1184 Genetiikka, kehitysbiologia, fysiologiafi_FI
dc.okm.internationalcopublicationinternational co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisherElsevier
dc.publisher.countryUnited Statesen_GB
dc.publisher.countryYhdysvallat (USA)fi_FI
dc.publisher.country-codeUS
dc.relation.doi10.1016/j.celrep.2017.07.036
dc.relation.ispartofjournalCell Reports
dc.relation.issue6
dc.relation.volume20
dc.source.identifierhttps://www.utupub.fi/handle/10024/161083
dc.titleEpigenomic Landscapes of hESC-Derived Neural Rosettes: Modeling Neural Tube Formation and Diseases
dc.year.issued2017

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