<HashMap><database>biostudies-arrayexpress</database><scores/><additional><omics_type>Metabolomics</omics_type><omics_type>Unknown</omics_type><omics_type>Transcriptomics</omics_type><omics_type>Genomics</omics_type><omics_type>Proteomics</omics_type><submitter>Christopher Hoyle</submitter><instrument_platform>Illumina NovaSeq 6000</instrument_platform><study_type>RNA-seq of total RNA</study_type><organism>Mus musculus</organism><species>Mus musculus</species><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/E-MTAB-16641</full_dataset_link><description>We generated a mouse with a mutated IL-1alpha nuclear localisation sequence, causing loss of pro-IL-1alpha nuclear localisation. We tested whether this loss of nuclear pro-IL-1alpha affected the transcriptional response of primary BMDMs to LPS priming.  Primary BMDMs from WT or mNLS mice were treated with vehicle or LPS (1ug/ml, 4h).</description><repository>biostudies-arrayexpress</repository><sample_protocol>Library Construction - Illumina TruSeq Stranded mRNA kit, according to the manufacturer’s protocol.</sample_protocol><sample_protocol>Sequencing - Sequenced paired end 59bp on NOVASEQ6000 at the Genomic Technologies Core Facility University of Manchester.</sample_protocol><sample_protocol>Nucleic Acid Extraction - Total RNA was extracted using a PureLink RNA mini kit.</sample_protocol><sample_protocol>Sample Collection - Primary BMDMs from WT or mNLS mice were treated with vehicle or LPS (1ug/ml, 4h). Supernatant was aspirated, cells washed once with PBS, and then lysis buffer containing 1% mercaptoethanol was added.</sample_protocol><figure_sub>Organization</figure_sub><figure_sub>MINSEQE Score</figure_sub><figure_sub>Assays and Data</figure_sub><figure_sub>MAGE-TAB Files</figure_sub><pubmed_authors>Christopher Hoyle</pubmed_authors></additional><is_claimable>false</is_claimable><name>RNA-Seq of vehicle- vs LPS-treated primary BMDMs from WT or interleukin-1alpha nuclear localisation sequence mutant mice</name><description>We generated a mouse with a mutated IL-1alpha nuclear localisation sequence, causing loss of pro-IL-1alpha nuclear localisation. We tested whether this loss of nuclear pro-IL-1alpha affected the transcriptional response of primary BMDMs to LPS priming.  Primary BMDMs from WT or mNLS mice were treated with vehicle or LPS (1ug/ml, 4h).</description><dates><release>2026-02-28T00:00:00Z</release><modification>2026-02-28T02:02:20.947Z</modification><creation>2026-02-11T12:11:00.129Z</creation></dates><accession>E-MTAB-16641</accession><cross_references><ENA>ERP188995</ENA><EFO>EFO_0002944</EFO><EFO>EFO_0004170</EFO><EFO>EFO_0009653</EFO><EFO>EFO_0005518</EFO><EFO>EFO_0004184</EFO></cross_references></HashMap>