Cargando…

Foxm1 transcription factor is required for maintenance of pluripotency of P19 embryonal carcinoma cells

Transcription factor Foxm1 plays a critical role during embryonic development and its expression is repressed during retinoic acid (RA)-induced differentiation of pluripotent P19 embryonal carcinoma cells at the early stage, correlated with downregulation of expression of pluripotency markers. To st...

Descripción completa

Detalles Bibliográficos
Autores principales:	Xie, Zhongqiu, Tan, Guixiang, Ding, Miao, Dong, Difei, Chen, Tuanhui, Meng, Xiangxian, Huang, Xiaoqin, Tan, Yongjun
Formato:	Texto
Lenguaje:	English
Publicado:	Oxford University Press 2010
Materias:	Gene Regulation, Chromatin and Epigenetics
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3001083/ https://www.ncbi.nlm.nih.gov/pubmed/20702419 http://dx.doi.org/10.1093/nar/gkq715

Ejemplares similares

Sin3a–Tet1 interaction activates gene transcription and is required for embryonic stem cell pluripotency
por: Zhu, Fugui, et al.
Publicado: (2018)

Evaluation of the determinants for improved pluripotency induction and maintenance by engineered SOX17
por: Hu, Haoqing, et al.
Publicado: (2023)

HDAC1 regulates pluripotency and lineage specific transcriptional networks in embryonic and trophoblast stem cells
por: Kidder, Benjamin L., et al.
Publicado: (2012)

A hyperdynamic H3.3 nucleosome marks promoter regions in pluripotent embryonic stem cells
por: Schlesinger, Sharon, et al.
Publicado: (2017)

HP1γ regulates H3K36 methylation and pluripotency in embryonic stem cells
por: Zaidan, Nur Zafirah, et al.
Publicado: (2020)

PML bodies provide an important platform for the maintenance of telomeric chromatin integrity in embryonic stem cells
por: Chang, Fiona T. M., et al.
Publicado: (2013)

A novel requirement for DROSHA in maintenance of mammalian CG methylation
por: Stathopoulou, Athanasia, et al.
Publicado: (2017)

Relaxed 3D genome conformation facilitates the pluripotent to totipotent-like state transition in embryonic stem cells
por: Zhu, Yezhang, et al.
Publicado: (2021)

The tail-module of yeast Mediator complex is required for telomere heterochromatin maintenance
por: Peng, Jing, et al.
Publicado: (2012)

GCNA is a histone binding protein required for spermatogonial stem cell maintenance
por: Ribeiro, Jonathan, et al.
Publicado: (2023)

Transcriptional network dynamics during the progression of pluripotency revealed by integrative statistical learning
por: Kim, Hani Jieun, et al.
Publicado: (2020)

CstF-64 supports pluripotency and regulates cell cycle progression in embryonic stem cells through histone 3′ end processing
por: Youngblood, Bradford A., et al.
Publicado: (2014)

An epigenetic switch regulates de novo DNA methylation at a subset of pluripotency gene enhancers during embryonic stem cell differentiation
por: Petell, Christopher J., et al.
Publicado: (2016)

G-quadruplexes as novel cis-elements controlling transcription during embryonic development
por: David, Aldana P., et al.
Publicado: (2016)

Set7 mediated interactions regulate transcriptional networks in embryonic stem cells
por: Tuano, Natasha K., et al.
Publicado: (2016)

Yin Yang 1 extends the Myc-related transcription factors network in embryonic stem cells
por: Vella, Pietro, et al.
Publicado: (2012)

Targeted transcriptional activation of silent oct4 pluripotency gene by combining designer TALEs and inhibition of epigenetic modifiers
por: Bultmann, Sebastian, et al.
Publicado: (2012)

Requirement of CRTC1 coactivator for hepatitis B virus transcription
por: Tang, Hei-Man Vincent, et al.
Publicado: (2014)

Activation of transcription factor circuity in 2i-induced ground state pluripotency is independent of repressive global epigenetic landscapes
por: Shukla, Ruchi, et al.
Publicado: (2020)

Modeling the relative relationship of transcription factor binding and histone modifications to gene expression levels in mouse embryonic stem cells
por: Cheng, Chao, et al.
Publicado: (2012)

Nono deficiency compromises TET1 chromatin association and impedes neuronal differentiation of mouse embryonic stem cells
por: Li, Wenjing, et al.
Publicado: (2020)

The forkhead transcription factor FOXK2 premarks lineage-specific genes in human embryonic stem cells for activation during differentiation
por: Ji, Zongling, et al.
Publicado: (2021)

Differential coregulator requirements for function of the hematopoietic transcription factor GATA-1 at endogenous loci
por: Pope, Nathaniel J., et al.
Publicado: (2010)

TFIIS is required for the balanced expression of the genes encoding ribosomal components under transcriptional stress
por: Gómez-Herreros, Fernando, et al.
Publicado: (2012)

Histone deacetylase 3 controls a transcriptional network required for B cell maturation
por: Stengel, Kristy R, et al.
Publicado: (2019)

HDAC1 is required for GATA-1 transcription activity, global chromatin occupancy and hematopoiesis
por: Yan, Bowen, et al.
Publicado: (2021)

Suppression of intragenic transcription requires the MOT1 and NC2 regulators of TATA-binding protein
por: Koster, Maria J. E., et al.
Publicado: (2014)

The SIN3A histone deacetylase complex is required for a complete transcriptional response to hypoxia
por: Tiana, Maria, et al.
Publicado: (2018)

Transcription factor Tcf4 is the preferred heterodimerization partner for Olig2 in oligodendrocytes and required for differentiation
por: Wedel, Miriam, et al.
Publicado: (2020)

A genetic analysis reveals novel histone residues required for transcriptional reprogramming upon stress
por: Viéitez, Cristina, et al.
Publicado: (2020)

Thyroid hormone dependent transcriptional programming by TRβ requires SWI/SNF chromatin remodelers
por: Gillis, Noelle E, et al.
Publicado: (2022)

H3K4 demethylase KDM5B regulates global dynamics of transcription elongation and alternative splicing in embryonic stem cells
por: He, Runsheng, et al.
Publicado: (2017)

A primary role of TET proteins in establishment and maintenance of De Novo bivalency at CpG islands
por: Kong, Lingchun, et al.
Publicado: (2016)

The dimerization domain of SOX9 is required for transcription activation of a chondrocyte-specific chromatin DNA template
por: Coustry, Françoise, et al.
Publicado: (2010)

The chromatin remodeller CHD8 is required for E2F-dependent transcription activation of S-phase genes
por: Subtil-Rodríguez, Alicia, et al.
Publicado: (2014)

Tetramerization of MADS family transcription factors SEPALLATA3 and AGAMOUS is required for floral meristem determinacy in Arabidopsis
por: Hugouvieux, Véronique, et al.
Publicado: (2018)

Single-cell profiling reveals that eRNA accumulation at enhancer–promoter loops is not required to sustain transcription
por: Rahman, Samir, et al.
Publicado: (2017)

The conserved elongation factor Spn1 is required for normal transcription, histone modifications, and splicing in Saccharomyces cerevisiae
por: Reim, Natalia I, et al.
Publicado: (2020)

Promoter RNA links transcriptional regulation of inflammatory pathway genes
por: Matsui, Masayuki, et al.
Publicado: (2013)

Activated transcription via mammalian amino acid response elements does not require enhanced recruitment of the Mediator complex
por: Thiaville, Michelle M., et al.
Publicado: (2008)

Cannot write session to /tmp/vufind_sessions/sess_js7g3aprad70dv2knp9etj7le6