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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="GSM1009613 1"/></item><item><item key="GSM1009614 1"/></item></item><item key="id">7032</item><item key="ownerprofile_id">arrayexpress_sid</item><item key="platform">6</item><item key="summary_wrapped">Box C/D-type small nucleolar RNAs (snoRNAs) are functional RNAs responsible for mediating 2&#8217;-O-ribose methylation of ribosomal RNAs...</item><item key="geo_gse_id">E-GEOD-41164</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>b-cell lymphoma</item><item>cell</item><item>intron</item><item>lymphoma</item><item>nucleolus</item><item>protein</item></item><item key="lastmodified">Dec.12, 2014</item><item key="is_default">False</item><item key="geo_id_plat">E-GEOD-41164_A-AFFY-45</item><item key="slug">expression-data-from-splenic-b-cells-isolated-from</item><item key="geo_gds_id"/><item key="name">Expression data from splenic B-cells isolated from DmU50(HG-b) mice or wild-type C57BL/6J</item><item key="created">Nov.12, 2014</item><item key="summary">Box C/D-type small nucleolar RNAs (snoRNAs) are functional RNAs responsible for mediating 2&#8217;-O-ribose methylation of ribosomal RNAs (rRNAs) within the nucleolus. Previously, in relation to a novel chromosomal translocation in a human B-cell lymphoma, we identified U50HG, a non-protein-coding gene that hosted a box C/D-type U50 snoRNA within its intron. To investigate the physiological importance of the U50 snoRNA and its involvement in tumorigenesis, we generated a mouse model deficient in mouse U50 (mU50) snoRNA expression without altering the expression of mouse mU50 host-gene, mU50HG-b. The established mU50 snoRNA-deficient mice showed a significant reduction of mU50 snoRNA expression and the corresponding target rRNA methylation in various organs. Lifelong phenotypic monitoring showed that the mU50-deficient mice looked almost normal without accelerated tumorigenicity; however, a notable difference was the propensity for anomalies in the lymphoid organs. B-cells were isolated from spleens of DmU50(HG-b) mice or wild-type C57BL/6J with antibody-conjugated magnetic beads system (Myltenyi Biotec). Total RNA was purified with QIAGEN RNeasy Micro kit. Affymetrix GeneChip&#174; Microarrays (Mouse Expression 430 2.0 Array) were used.</item><item key="source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-41164</item><item key="sample_source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-41164/samples/</item></data></biogps>
