Human Gene Set: TESAR_ALK_AND_JAK_TARGETS_MOUSE_ES_D4_DN

For the Mouse gene set with the same name, see TESAR_ALK_AND_JAK_TARGETS_MOUSE_ES_D4_DN

Standard name TESAR_ALK_AND_JAK_TARGETS_MOUSE_ES_D4_DN
Systematic name M1764
Brief description Genes down-regulated in mES cells (mouse embryonic stem cells) after tratment with the ALK [GeneID=238] inhibitor SB-431542 and JAK inhibitor I [PubChem=4521392;5494425].
Full description or abstract The application of human embryonic stem (ES) cells in medicine and biology has an inherent reliance on understanding the starting cell population. Human ES cells differ from mouse ES cells and the specific embryonic origin of both cell types is unclear. Previous work suggested that mouse ES cells could only be obtained from the embryo before implantation in the uterus. Here we show that cell lines can be derived from the epiblast, a tissue of the post-implantation embryo that generates the embryo proper. These cells, which we refer to as EpiSCs (post-implantation epiblast-derived stem cells), express transcription factors known to regulate pluripotency, maintain their genomic integrity, and robustly differentiate into the major somatic cell types as well as primordial germ cells. The EpiSC lines are distinct from mouse ES cells in their epigenetic state and the signals controlling their differentiation. Furthermore, EpiSC and human ES cells share patterns of gene expression and signalling responses that normally function in the epiblast. These results show that epiblast cells can be maintained as stable cell lines and interrogated to understand how pluripotent cells generate distinct fates during early development.
Collection C2: Curated
      CGP: Chemical and Genetic Perturbations
Source publication Pubmed 17597760   Authors: Tesar PJ,Chenoweth JG,Brook FA,Davies TJ,Evans EP,Mack DL,Gardner RL,McKay RD
Exact source Table 1S: mES d4 +SB431542 & JAK Inh.
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Source species Mus musculus
Contributed by Jessica Robertson (MSigDB Team)
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MOUSE_GENE_SYMBOL
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Version history 3.1: First introduced

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