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<biogps><data><item key="platform">6</item><item key="owner">ArrayExpress Uploader</item><item key="pop_total">0</item><item key="species">mouse</item><item key="factors"><item><item key="GSM723804"><item key="AGE">4 weeks after birth</item><item key="CELL TYPE">VSEL</item><item key="STRAIN OR LINE">C57BL/6</item></item></item><item><item key="GSM723804"><item key="AGE">4 weeks after birth</item><item key="CELL TYPE">VSEL</item><item key="STRAIN OR LINE">C57BL/6</item></item></item><item><item key="GSM723804"><item key="AGE">4 weeks after birth</item><item key="CELL TYPE">VSEL</item><item key="STRAIN OR LINE">C57BL/6</item></item></item><item><item key="GSM723807"><item key="AGE">4 weeks after birth</item><item key="CELL TYPE">HSC</item><item key="STRAIN OR LINE">C57BL/6</item></item></item><item><item key="GSM723807"><item key="AGE">4 weeks after birth</item><item key="CELL TYPE">HSC</item><item key="STRAIN OR LINE">C57BL/6</item></item></item><item><item key="GSM723807"><item key="AGE">4 weeks after birth</item><item key="CELL TYPE">HSC</item><item key="STRAIN OR LINE">C57BL/6</item></item></item><item><item key="GSM723810"><item key="AGE">embryo before implantation</item><item key="CELL TYPE">not specified</item><item key="STRAIN OR LINE">129S2/SvPas</item></item></item><item><item key="GSM723810"><item key="AGE">embryo before implantation</item><item key="CELL TYPE">not specified</item><item key="STRAIN OR LINE">129S2/SvPas</item></item></item><item><item key="GSM723810"><item key="AGE">embryo before implantation</item><item key="CELL TYPE">not specified</item><item key="STRAIN OR LINE">129S2/SvPas</item></item></item></item><item key="id">6471</item><item key="ownerprofile_id">arrayexpress_sid</item><item key="source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-29281</item><item key="summary_wrapped">Recently, we identified a population of Oct4+Sca-1+Lin-CD45- very small embryonic-like stem-cells (VSELs) in adult tissues. Open...</item><item key="pubmed_id">22023227</item><item key="owner_profile">/profile/8773/arrayexpressuploader</item><item key="factor_count">3</item><item key="sample_count">9</item><item key="tags"><item>bone</item><item>cell</item><item>chromatin</item><item>genome</item><item>protein</item></item><item key="lastmodified">Dec.12, 2014</item><item key="is_default">False</item><item key="geo_gds_id"/><item key="slug">single-cell-based-genomewide-gene-expression-analy</item><item key="geo_id_plat">E-GEOD-29281_A-AFFY-45</item><item key="name">Single Cell based genomewide gene expression analysis of murine bone-marrow derived Very Small Embryonic-Like Stem Cells (VSELs)</item><item key="created">Nov.11, 2014</item><item key="summary">Recently, we identified a population of Oct4+Sca-1+Lin-CD45- very small embryonic-like stem-cells (VSELs) in adult tissues. Open chromatin structure of pluripotency genes and genomic imprinting-related epigenetic mechanisms maintain pluripotency and quiescence of VSELs, respectively. However, global transcriptome signature of this rare stem-cell population remains elusive. Here, we demonstrate by genomewide gene-expression analysis with a small number of highly purified murine bone-marrow (BM)-derived VSELs, that Oct4+ VSELs i) express a similar, yet nonidentical, transcriptome as embryonic stem-cells (ESCs), ii) up-regulate cell-cycle checkpoint genes, iii) down-regulate genes involved in protein turnover and mitogenic pathways, and iv) highly express Ezh2, a polycomb group protein. Furthermore, as a result of Ezh2 overexpression, VSELs, like ESCs, exhibit bivalently modified nucleosomes (trimethylated H3K27 and H3K4) at promoters of important homeodomain-containing developmental transcription factors, thus preventing their premature transcription. Notably, spontaneous or RNA interference-enforced down-regulation of Ezh2 during VSEL differentiation removes the bivalent-domain (BD) structure, which leads to de-repression of several BD-regulated genes. Therefore, we suggest that VSELs, like other pluripotent stem-cells, maintain their pluripotent state through an Ezh2-dependent BD-mediated epigenetic mechanism. T7-primed cDNA libraries was synthesized using FACS sorted twenty cells. T7-primed libraries were biotin-labeled using the GeneChip 3&#8217; in vitro transcription (IVT) kit (Affymetrix), starting from &#8216;&#8216;In vitro Transcription to Synthesize Labeled aRNA. Nine Samples (3 VSELs, 3 HSC, and 3 ESC-D3) are analyzed using GeneChip 3&#8217; Mouse Genome 430 2.0 array (Affymetrix), according to the manufacturer&#8217;s instructions.</item><item key="geo_gse_id">E-GEOD-29281</item><item key="sample_source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-29281/samples/</item></data></biogps>
