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<biogps><data><item key="owner">ArrayExpress Uploader</item><item key="pop_total">0</item><item key="species">mouse</item><item key="factors"><item><item key="GSM474645 1"/></item><item><item key="GSM474646 1"/></item></item><item key="id">8249</item><item key="ownerprofile_id">arrayexpress_sid</item><item key="platform">7</item><item key="summary_wrapped">Understanding the mechanism by which embryonic stem (ES) cells self-renew is critical for the realization of their therapeutic potential....</item><item key="geo_gse_id">E-GEOD-19144</item><item key="owner_profile">/profile/8773/arrayexpressuploader</item><item key="factor_count">0</item><item key="sample_count">2</item><item key="tags"><item>cell</item><item>serum</item></item><item key="lastmodified">Dec.12, 2014</item><item key="is_default">False</item><item key="geo_gds_id"/><item key="slug">id1-maintains-embryonic-stem-cell-self-renewal-by</item><item key="geo_id_plat">E-GEOD-19144_A-AFFY-23</item><item key="name">Id1 maintains embryonic stem cell self-renewal by upregulation of Nanog and repression of Brachyury expression</item><item key="created">Nov.23, 2014</item><item key="summary">Understanding the mechanism by which embryonic stem (ES) cells self-renew is critical for the realization of their therapeutic potential.  Previously it had been shown that in combination with LIF, Id proteins were sufficient to maintain mouse ES cells in a self-renewing state.  Here we investigate the requirement for Id1 in maintaing ES cell self-renewal and blocking differentiation.  We find that Id1-/- ES cells have a propensity to differentiate and a decreased capacity to self-renew.  Chronic or acute loss of Id1 leads to a down-regulation of Nanog, a critical regulator of self-renewal.  In addition, in the absence of Id1, ES cells express elevated levels of Brachyury, a marker of mesendoderm differentiation.  We find that loss of both Nanog and Id1 is required for the up-regulation of Brachyury, and Id1 maintains Nanog expression by blocking the expression of Zeb1, a repressor of Nanog transcription.  These results identify Id1 as an important factor in the maintenance of ES cell self-renewal and suggest a plausible mechanism for its control of lineage commitment. Wild type and Id1-/- ES cells were grown on gelatin under normal self-renewing conditions (in the presence of serum and LIF).</item><item key="source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-19144</item><item key="sample_source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-19144/samples/</item></data></biogps>
