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<biogps><data><item key="owner">ArrayExpress Uploader</item><item key="ownerprofile_id">arrayexpress_sid</item><item key="species">human</item><item key="factors"><item><item key="GSM841045"><item key="TREATMENT">control</item></item></item><item><item key="GSM841046"><item key="TREATMENT">Tamoxifen induced</item></item></item><item><item key="GSM841047"><item key="TREATMENT">shRNA SAE2</item></item></item><item><item key="GSM841048"><item key="TREATMENT">Tamoxifen+shRNA</item></item></item><item><item key="GSM841045"><item key="TREATMENT">control</item></item></item><item><item key="GSM841046"><item key="TREATMENT">Tamoxifen induced</item></item></item><item><item key="GSM841047"><item key="TREATMENT">shRNA SAE2</item></item></item><item><item key="GSM841048"><item key="TREATMENT">Tamoxifen+shRNA</item></item></item><item><item key="GSM841045"><item key="TREATMENT">control</item></item></item><item><item key="GSM841046"><item key="TREATMENT">Tamoxifen induced</item></item></item><item><item key="GSM841047"><item key="TREATMENT">shRNA SAE2</item></item></item><item><item key="GSM841048"><item key="TREATMENT">Tamoxifen+shRNA</item></item></item></item><item key="id">4328</item><item key="pop_total">0</item><item key="platform">4</item><item key="summary_wrapped">Myc is an oncogenic transcription factor frequently dysregulated in human cancer. To identify pathways supporting the Myc oncogenic...</item><item key="geo_gse_id">E-GEOD-34055</item><item key="owner_profile">/profile/8773/arrayexpressuploader</item><item key="factor_count">1</item><item key="sample_count">12</item><item key="tags"><item>cancer</item><item>genome</item><item>spindle</item></item><item key="lastmodified">Dec.12, 2014</item><item key="is_default">False</item><item key="geo_id_plat">E-GEOD-34055_A-AFFY-44</item><item key="slug">a-sumoylation-dependent-transcriptional-subprogram</item><item key="geo_gds_id"/><item key="name">A sumoylation-dependent transcriptional subprogram is required for Myc-driven tumorigenesis</item><item key="created">Sep.16, 2014</item><item key="summary">Myc is an oncogenic transcription factor frequently dysregulated in human cancer. To identify pathways supporting the Myc oncogenic program, we employed a genome-wide RNAi screen for Myc-synthetic-lethal (MySL) genes and uncovered a role for the SUMO-activating-enzyme (SAE1/2). Loss of SAE1/2 enzymatic activity drives synthetic lethality with Myc.  Mechanistically, SAE2 inhibition switches a transcriptional subprogram of Myc from activated to repressed. A subset of these SUMOylation-dependent Myc-switchers (SMS genes) governs mitotic spindle function and is required to support the Myc oncogenic program. comparison of 4 treatments: normal HMEC, High Myc in HMEC, SUMO depleted in HMEC, High Myc+Sumo Depleted in HMEC</item><item key="source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-34055</item><item key="sample_source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-34055/samples/</item></data></biogps>
