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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="GSE16751GSM419953"/></item><item><item key="GSE16751GSM419954"/></item><item><item key="GSE16751GSM419955"/></item><item><item key="GSE16751GSM419956"/></item><item><item key="GSE16751GSM419957"/></item><item><item key="GSE16751GSM419958"/></item></item><item key="id">5739</item><item key="ownerprofile_id">arrayexpress_sid</item><item key="platform">6</item><item key="summary_wrapped">Activation-Induced Cytidine Deaminase (AID) is required for somatic hypermutation and immunoglobulin (Ig) class switch recombination in...</item><item key="geo_gse_id">E-GEOD-16751</item><item key="owner_profile">/profile/8773/arrayexpressuploader</item><item key="factor_count">0</item><item key="sample_count">6</item><item key="tags"><item>acute lymphoblastic leukemia</item><item>bone</item><item>bone marrow</item><item>cell</item><item>class</item><item>immunoglobulin</item><item>leukemia</item><item>lymphoblastic leukemia</item></item><item key="lastmodified">Dec.12, 2014</item><item key="is_default">False</item><item key="geo_gds_id"/><item key="slug">transcription-profiling-of-aid-expressing-leukemia</item><item key="geo_id_plat">E-GEOD-16751_A-AFFY-45</item><item key="name">Transcription profiling of AID expressing leukemia and AID deficient leukemia in a mouse model of BCR-ABL1 ALL</item><item key="created">Nov.11, 2014</item><item key="summary">Activation-Induced Cytidine Deaminase (AID) is required for somatic hypermutation and immunoglobulin (Ig) class switch recombination in germinal center B lymphocytes.  Occasionally, AID targets non-Ig genes, thereby contributing to B cell lymphomagenesis.  We recently reported aberrant expression of AID in BCR-ABL1-driven acute lymphoblastic leukemia (ALL).  To elucidate the biological significance of aberrant AID expression, we studied loss of AID function in a murine model of BCR-ABL1 ALL.  Mice transplanted with BCR-ABL1-transduced AID-/- bone marrow had prolonged survival as compared to mice transplanted with leukemia cells generated from AID+/+ bone marrow.  Consistent with a causative role of AID in genetic instability, AID-/- leukemia had a decreased frequency of amplifications, deletions and a lower frequency of mutations in non-Ig genes including Pax5 and Rhoh as compared to AID+/+ leukemias.  AID-/- and AID+/+ ALL cells showed a markedly distinct gene expression pattern as determined by principle component analysis, with 2,365 genes differentially expressed.  In contrast to AID+/+ leukemia, AID-/- ALL cells failed to downregulate a number of tumor suppressor genes such as Rhoh, Cdkn1a (p21), and Blnk (SLP65).  We conclude that AID accelerates clonal evolution in BCR-ABL1 ALL by enhancing genetic instability, aberrant somatic hypermutation, and by transcriptional inactivation of tumor suppressor genes. Experiment Overall Design: We used microarrays to detect differences in gene expression profiles between AID expressing leukemia and AID deficient leukemia</item><item key="source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-16751</item><item key="sample_source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-16751/samples/</item></data></biogps>
