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<biogps><data><item key="owner">ArrayExpress Uploader</item><item key="pop_total">0</item><item key="species">human</item><item key="factors"><item><item key="GSM758764 1"/></item><item><item key="GSM758765 1"/></item><item><item key="GSM758766 1"/></item><item><item key="GSM758767 1"/></item><item><item key="GSM758768 1"/></item><item><item key="GSM758769 1"/></item><item><item key="GSM758770 1"/></item><item><item key="GSM758771 1"/></item><item><item key="GSM758772 1"/></item><item><item key="GSM758773 1"/></item><item><item key="GSM758774 1"/></item><item><item key="GSM758775 1"/></item></item><item key="id">4168</item><item key="ownerprofile_id">arrayexpress_sid</item><item key="platform">4</item><item key="summary_wrapped">Homodimerization of Mpl can also be accomplished in the absence of Tpo, by binding of a synthetic ligand (Chemical inducer of...</item><item key="geo_gse_id">E-GEOD-30585</item><item key="owner_profile">/profile/8773/arrayexpressuploader</item><item key="factor_count">0</item><item key="sample_count">12</item><item key="tags"><item>protein</item><item>stroma</item></item><item key="lastmodified">Dec.12, 2014</item><item key="is_default">False</item><item key="geo_gds_id"/><item key="slug">gene-expression-changes-induced-by-dimerization-of</item><item key="geo_id_plat">E-GEOD-30585_A-AFFY-44</item><item key="name">Gene expression changes induced by dimerization of intracellular c-Mpl in cord blood CD34+ progenitors</item><item key="created">Sep.16, 2014</item><item key="summary">Homodimerization of Mpl can also be accomplished in the absence of Tpo, by binding of a synthetic ligand (Chemical inducer of dimerization, CID) to a constitutively expressed fusion protein F36VMpl consisting of a ligand binding domain (F36V) and the intracellular signaling domain of Mpl. In contrast to Tpo stimulation, F36VMpl dimerization in human CD34+ progenitor cells generates robust erythropoiesis. Microarray gene expression profiling of progenitors demonstrated that F36VMpl dimerization, but not Tpo, results in upregulation of critical erythroid genes. CD34+ cord blood cells were transduced with F36VMpl-GFP (GFP reporter gene) and cultured on MS-5 stroma for 7 days in the presence of CID, Tpo, Epo or no factors (no CID, negative control). CD34+GFP+ cells were sorted on day 7 and subjected to microarray (n=3 independent experiments).</item><item key="source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-30585</item><item key="sample_source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-30585/samples/</item></data></biogps>
