Genome-Wide Studies Reveal that H3K4me3 Modification in Bivalent Genes Is Dynamically Regulated during the Pluripotent Cell Cycle and Stabilized upon Differentiation

Vista sencilla de ítem
dc.contributor.authorGrandy, R.
dc.contributor.authorWhitfield, T.W.
dc.contributor.authorWu, H.
dc.contributor.authorFitzgerald, M.P.
dc.contributor.authorVanOudenhove, J.J.
dc.contributor.authorZaidi, S.K.
dc.contributor.authorMontecino, M.A.
dc.contributor.authorLian, J.B.
dc.contributor.authorvan Wijnen, A.J.
dc.contributor.authorStein, J.L.
dc.contributor.authorStein, G.S.
dc.date.accessioned2017-08-17T20:19:17Z
dc.date.available2017-08-17T20:19:17Z
dc.date.issued2016-02
dc.descriptionIndexación: Web of Science; Scopus.es_CL
dc.description.abstractStem cell phenotypes are reflected by posttranslational histone modifications, and this chromatin-related memory must be mitotically inherited to maintain cell identity through proliferative expansion. In human embryonic stem cells (hESCs), bivalent genes with both activating (H3K4me3) and repressive (H3K27me3) histone modifications are essential to sustain pluripotency. Yet, the molecular mechanisms by which this epigenetic landscape is transferred to progeny cells remain to be established. By mapping genomic enrichment of H3K4me3/H3K27me3 in pure populations of hESCs in G2, mitotic, and G1 phases of the cell cycle, we found striking variations in the levels of H3K4me3 through the G2-M-G1 transition. Analysis of a representative set of bivalent genes revealed that chromatin modifiers involved in H3K4 methylation/demethylation are recruited to bivalent gene promoters in a cell cycle-dependent fashion. Interestingly, bivalent genes enriched with H3K4me3 exclusively during mitosis undergo the strongest upregulation after induction of differentiation. Furthermore, the histone modification signature of genes that remain bivalent in differentiated cells resolves into a cell cycle-independent pattern after lineage commitment. These results establish a new dimension of chromatin regulation important in the maintenance of pluripotencyes_CL
dc.description.urihttp://mcb.asm.org/content/36/4/615
dc.identifier.citationMol. Cell. Biol. February 2016 vol. 36 no. 4 615-627es_CL
dc.identifier.issn0270-7306
dc.identifier.other10.1128/MCB.00877-15
dc.identifier.urihttp://repositorio.unab.cl/xmlui/handle/ria/3966
dc.language.isoenes_CL
dc.publisherAmerican Society for Microbiologyes_CL
dc.subjectChromatines_CL
dc.subjectDNA binding proteines_CL
dc.subjectHistonees_CL
dc.subjectHistone lysine methyltransferasees_CL
dc.subjectMixed lineage leukemia proteines_CL
dc.subjectMLL protein, humanes_CL
dc.subjectMLL2 protein, humanes_CL
dc.subjectTumor proteines_CL
dc.titleGenome-Wide Studies Reveal that H3K4me3 Modification in Bivalent Genes Is Dynamically Regulated during the Pluripotent Cell Cycle and Stabilized upon Differentiationes_CL
dc.typeArtículoes_CL
Archivos
Bloque original
Mostrando 1 - 1 de 1
Miniatura
Nombre:
Grandy_R_Genome-Wide_Studies_Reveal.pdf
Tamaño:
3.74 MB
Formato:
Adobe Portable Document Format
Descripción:
TEXTO COMPLETO INGLES
Descargar
Bloque de licencias
Mostrando 1 - 1 de 1
No hay miniatura disponible
Nombre:
license.txt
Tamaño:
1.71 KB
Formato:
Item-specific license agreed upon to submission
Descripción:
Descargar
Colecciones
Fac.CV - Artículos de Revista
FM - Artículos de Revista