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PMID: 17211451 Published · ppublish English Journal Article Review

Nanog and transcriptional networks in embryonic stem cell pluripotency.

Cell research ·Vol. 17 ·No. 1 ·2007-01-00 ·Pages 42-9

Pan G, Thomson JA

Abstract

Several extrinsic signals such as LIF, BMP and Wnt can support the self-renewal and pluripotency of embryonic stem (ES) cells through regulating the "pluripotent genes." A unique homeobox transcription factor, Nanog, is one of the key downstream effectors of these signals. Elevated level of Nanog can maintain the mouse ES cell self-renewal independent of LIF and enable human ES cell growth without feeder cells. In addition to the external signal pathways, intrinsic transcription factors such as FoxD3, P53 and Oct4 are also involved in regulating the expression of Nanog. Functionally, Nanog works together with other key pluripotent factors such as Oct4 and Sox2 to control a set of target genes that have important functions in ES cell pluripotency. These key factors form a regulatory network to support or limit each other's expression level, which maintains the properties of ES cells.

MeSH Terms
Amino Acid Sequence Animals DNA-Binding Proteins/genetics,physiology Embryonic Stem Cells/cytology,metabolism,physiology Gene Expression Regulation, Developmental/physiology Homeodomain Proteins/genetics,physiology Humans Molecular Sequence Data Nanog Homeobox Protein Pluripotent Stem Cells/cytology,metabolism,physiology Transcription, Genetic/physiology
Chemicals
DNA-Binding Proteins Homeodomain Proteins NANOG protein, human Nanog Homeobox Protein
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Pan Guangjin
The Wisconsin National Primate Research Center, University of Wisconsin-Madison, 1220 Capitol Court, Madison, WI 53715-1299, USA. gpan@primate.wisc.edu
Thomson James A
Article Info
Journal
Cell research
Abbr.
Cell Res
ISSN
1748-7838
Published
2007-01-00
Pages
42-9
Language
English
Region
England
NLM ID
9425763
Subset
IM
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