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<biogps><data><item key="owner">ArrayExpress Uploader</item><item key="pop_total">0</item><item key="id">8054</item><item key="factors"><item><item key="BMM_ko-rep1"><item key="cell type">macrophage</item><item key="genotype">Upf2fl/fl;LysMCre</item></item></item><item><item key="BMM_ko-rep1"><item key="cell type">macrophage</item><item key="genotype">Upf2fl/fl;LysMCre</item></item></item><item><item key="BMM_ko-rep1"><item key="cell type">macrophage</item><item key="genotype">Upf2fl/fl;LysMCre</item></item></item><item><item key="BMM_wt-rep1"><item key="cell type">macrophage</item><item key="genotype">wild type genotype</item></item></item><item><item key="BMM_wt-rep1"><item key="cell type">macrophage</item><item key="genotype">wild type genotype</item></item></item><item><item key="BMM_wt-rep1"><item key="cell type">macrophage</item><item key="genotype">wild type genotype</item></item></item><item><item key="Thy_ko-rep1"><item key="cell type">thymocyte</item><item key="genotype">Upf2fl/fl;LckCre</item></item></item><item><item key="Thy_ko-rep1"><item key="cell type">thymocyte</item><item key="genotype">Upf2fl/fl;LckCre</item></item></item><item><item key="Thy_ko-rep1"><item key="cell type">thymocyte</item><item key="genotype">Upf2fl/fl;LckCre</item></item></item><item><item key="Thy_wt-rep1"><item key="cell type">thymocyte</item><item key="genotype">wild type genotype</item></item></item><item><item key="Thy_wt-rep1"><item key="cell type">thymocyte</item><item key="genotype">wild type genotype</item></item></item><item><item key="Thy_wt-rep1"><item key="cell type">thymocyte</item><item key="genotype">wild type genotype</item></item></item></item><item key="ownerprofile_id">arrayexpress_sid</item><item key="platform">6</item><item key="summary_wrapped">Knockdown experiments in transformed human cells, suggested that nonsense-mediated mRNA decay (NMD) components had extensive effects on...</item><item key="pubmed_id">18483223</item><item key="geo_gse_id">E-MEXP-1371</item><item key="owner_profile">/profile/8773/arrayexpressuploader</item><item key="factor_count">2</item><item key="sample_count">12</item><item key="tags"><item>cell</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-t-cell-thymocytes</item><item key="geo_id_plat">E-MEXP-1371_A-AFFY-45</item><item key="name">Transcription profiling of mouse T-cell thymocytes and bone marrow-derived macrophages dervied from Upf2fl/fl;LysMCre and Upf2fl/fl;LckCre mice to test the importance of nonsense-mediated mRNA decay on global transcription</item><item key="created">Nov.21, 2014</item><item key="summary">Knockdown experiments in transformed human cells, suggested that nonsense-mediated mRNA decay (NMD) components had extensive effects on the regulation of a significant fraction of the transcriptome   In order to test the importance of NMD on global transcription we subjected BMDMs and T-cell thymocytes derived from Upf2fl/fl;LysMCre and Upf2fl/fl;LckCre mice, respectively, to microarray-based gene expression profiling. Both these cell types display strong, if not complete, reduction of NMD as assayed by transfection with reporter constructs or sequencing of Tcrb transcripts. Upf2&#175;/&#175; BMDMs displayed significant changes in the expression of 182 genes (234 probe sets) of which 179 were upregulated.</item><item key="source">http://www.ebi.ac.uk/arrayexpress/experiments/E-MEXP-1371</item><item key="species">mouse</item><item key="sample_source">http://www.ebi.ac.uk/arrayexpress/experiments/E-MEXP-1371/samples/</item></data></biogps>
