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<biogps><data><item key="owner">ArrayExpress Uploader</item><item key="pop_total">0</item><item key="id">8366</item><item key="factors"><item><item key="GSE12356GSM310371"/></item><item><item key="GSE12356GSM310372"/></item><item><item key="GSE12356GSM310373"/></item><item><item key="GSE12356GSM310374"/></item><item><item key="GSE12356GSM310375"/></item><item><item key="GSE12356GSM310376"/></item><item><item key="GSE12356GSM310377"/></item><item><item key="GSE12356GSM310378"/></item></item><item key="ownerprofile_id">arrayexpress_sid</item><item key="platform">8</item><item key="summary_wrapped">The chromatin regulator Aiolos and the transcriptional coactivator OBF-1 have been implicated in regulating aspects of B cell maturation...</item><item key="pubmed_id">18974788</item><item key="geo_gse_id">E-GEOD-12356</item><item key="owner_profile">/profile/8773/arrayexpressuploader</item><item key="factor_count">0</item><item key="sample_count">8</item><item key="tags"><item>cell</item><item>chromatin</item><item>compartment</item><item>immunoglobulin</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-mouse-bone-marrow-with</item><item key="geo_id_plat">E-GEOD-12356_A-AFFY-36</item><item key="name">Transcription profiling of mouse bone marrow with Aiolos and OBF-1 deletions from 7 week old mice</item><item key="created">Nov.24, 2014</item><item key="summary">The chromatin regulator Aiolos and the transcriptional coactivator OBF-1 have been implicated in regulating aspects of B cell maturation and activation. Mice lacking either of these factors have a largely normal early B cell development. However, when both factors are eliminated simultaneously a block is uncovered at the transition between pre-B and immature B cells, indicating that these proteins exert a critical function in developing B lymphocytes. In mice deficient for Aiolos and OBF-1, the numbers of immature B cells are reduced, small pre-BII cells are increased and a significant impairment in immunoglobulin light chain DNA rearrangement is observed. We identified genes whose expression is deregulated in the pre-B cell compartment of these mice. In particular, we found that components of the pre-BCR, such as the surrogate light chain genes l5l5 and VpreB, fail to be efficiently silenced in double-mutant mice. Strikingly, developmentally regulated nuclear repositioning of the l5l5 gene is impaired in pre-B cells lacking OBF-1 and Aiolos. These studies uncover a novel role for OBF-1 and Aiolos in controlling the transcription and nuclear organization of genes involved in pre-BCR function. OBF-1 or Aiolos or both were deleted and the gene expression profiles for these animals investigated using Affymetrix arrays Experiment Overall Design: Two control wildtype animals, then duplicates for each of the single Aiolos or OBF-1 mutants and further duplicates for the Aiolos/OBF-1 double mutants</item><item key="source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-12356</item><item key="species">mouse</item><item key="sample_source">http://www.ebi.ac.uk/arrayexpress/experiments/E-GEOD-12356/samples/</item></data></biogps>
