dc.contributor.authorFang, Hai-Tong
dc.contributor.authorEL Farran, Chadi A.
dc.contributor.authorXing, Qiao Rui
dc.contributor.authorZhang, Li-Feng
dc.contributor.authorLi, Hu
dc.contributor.authorLim, Bing
dc.contributor.authorLoh, Yuin-Han
dc.date.accessioned2018-07-27T04:03:32Z
dc.date.available2018-07-27T04:03:32Z
dc.date.issued2018
dc.identifier.citationFang, H.-T., EL Farran, C. A., Xing, Q. R., Zhang, L.-F., Li, H., Lim, B., et al. (2018). Global H3.3 dynamic deposition defines its bimodal role in cell fate transition. Nature Communications, 9(1) 1537-.en_US
dc.identifier.urihttp://hdl.handle.net/10220/45296
dc.description.abstractH3.3 is a histone variant, which is deposited on genebodies and regulatory elements, by Hira, marking active transcription. Moreover, H3.3 is deposited on heterochromatin by Atrx/Daxx complex. The exact role of H3.3 in cell fate transition remains elusive. Here, we investigate the dynamic changes in the deposition of the histone variant H3.3 during cellular reprogramming. H3.3 maintains the identities of the parental cells during reprogramming as its removal at early time-point enhances the efficiency of the process. We find that H3.3 plays a similar role in transdifferentiation to hematopoietic progenitors and neuronal differentiation from embryonic stem cells. Contrastingly, H3.3 deposition on genes associated with the newly reprogrammed lineage is essential as its depletion at the later phase abolishes the process. Mechanistically, H3.3 deposition by Hira, and its K4 and K36 modifications are central to the role of H3.3 in cell fate conversion. Finally, H3.3 safeguards fibroblast lineage by regulating Mapk cascade and collagen synthesis.en_US
dc.description.sponsorshipNRF (Natl Research Foundation, S’pore)en_US
dc.description.sponsorshipASTAR (Agency for Sci., Tech. and Research, S’pore)en_US
dc.description.sponsorshipNMRC (Natl Medical Research Council, S’pore)en_US
dc.description.sponsorshipMOH (Min. of Health, S’pore)en_US
dc.format.extent17 p.en_US
dc.language.isoenen_US
dc.relation.ispartofseriesNature Communicationsen_US
dc.rights© 2018 The Author(s). This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.en_US
dc.subjectCell Fate Transitionen_US
dc.subjectDynamic Depositionen_US
dc.titleGlobal H3.3 dynamic deposition defines its bimodal role in cell fate transitionen_US
dc.typeJournal Article
dc.contributor.schoolSchool of Biological Sciencesen_US
dc.identifier.doihttp://dx.doi.org/10.1038/s41467-018-03904-7
dc.description.versionPublished versionen_US


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