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Expression data from TFIIA-non-cleavable mouse fetal liver hematopoietic stem cells

ABSTRACT: During embryogenesis, development of hematopoietic stem cells (HSC) occurs in the fetal liver and involves coordinate programs of transcription. Taspase1, a highly conserved threonine protease, directly cleaves and regulates the TFIIA families of transcription factors. We discovered that loss of Taspase1 (Tasp1-/-) or non-cleavage of TFIIAα−β (TFIIAα-βnc/nc) leads to a severe fetal liver developmental retardation that is associated with impaired HSC self-renewal and loss of HSC quiescence. We used microarray to elucidate the mechanism(s) by which TFIIA regulates fetal liver hematopoiesis, and expression of targets of HoxA9 was found to be altered by gene set enrichment analyses.

ORGANISM(S): Mus musculus

PROVIDER: GSE47422 | GEO | 2014/05/28

SECONDARY ACCESSION(S): PRJNA205539

REPOSITORIES: GEO

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Expression data from TFIIA-non-cleavable mouse fetal liver hematopoietic stem cells

Project description:During embryogenesis, development of hematopoietic stem cells (HSC) occurs in the fetal liver and involves coordinate programs of transcription. Taspase1, a highly conserved threonine protease, directly cleaves and regulates the TFIIA families of transcription factors. We discovered that loss of Taspase1 (Tasp1-/-) or non-cleavage of TFIIAa-b (TFIIAa-b nc/nc) leads to a severe fetal liver developmental retardation that is associated with impaired HSC self-renewal and loss of HSC quiescence. We used microarray to elucidate the mechanism(s) by which TFIIA regulates fetal liver hematopoiesis, and expression of targets of HoxA9 was found to be altered by gene set enrichment analyses. Embryonic day 14.5 fetal liver HSCs (defined as Lineage-Sca-1+c-Kit+CD150+cells) of wild-type (n = 4) and TFIIAa-b nc/nc (n = 3) were analyzed.

2014-05-28 | E-GEOD-47422 | biostudies-arrayexpress

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Mus musculus

Project description:Expression data from TFIIA-non-cleavable mouse fetal liver hematopoietic stem cells

| PRJNA205539 | ENA

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