<HashMap><database>biostudies-arrayexpress</database><scores/><additional><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-16640</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 response of these mice to Influenza A infection.  WT or mNLS mice were anaesthetized by 2.5% inhalation isoflurane and intranasally infected with 10^3 PFU of the IAV strain X31 (H3N2), in a volume of 30 µL PBS, on day 0. Infected WT and mNLS mice, and heterozygous control uninfected mice, were culled on day 7 post-IAV X31 infection, and the lung RNA was extracted.</description><repository>biostudies-arrayexpress</repository><sample_protocol>Library Construction - Illumina TruSeq Stranded mRNA kit, according to the manufacturer’s protocol.</sample_protocol><sample_protocol>Sample Collection - Infected WT, mNLS, and heterozygous control mice were culled on day 7 post-IAV X31 (H3N2) infection. One lung lobe was collected and placed in RNAlater stabilisation solution prior to subsequent RNA extraction.</sample_protocol><sample_protocol>Sequencing - Sequenced paired end 76bp on NOVASEQ6000 at the Genomic Technologies Core Facility University of Manchester</sample_protocol><sample_protocol>Nucleic Acid Extraction - Total RNA was extracted by transferring to a 2 mL tube containing RLT buffer supplemented with β-mercaptoethanol and a single 2 mm stainless steel bead. Tissue was homogenised into suspension using a Qiagen Tissue Lyser. Total RNA was then extracted using the RNeasy Mini Kit according to the manufacturer's protocol.</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 lung tissue from WT or interleukin-1alpha nuclear localisation sequence mutant mice infected with influenza A</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 response of these mice to Influenza A infection.  WT or mNLS mice were anaesthetized by 2.5% inhalation isoflurane and intranasally infected with 10^3 PFU of the IAV strain X31 (H3N2), in a volume of 30 µL PBS, on day 0. Infected WT and mNLS mice, and heterozygous control uninfected mice, were culled on day 7 post-IAV X31 infection, and the lung RNA was extracted.</description><dates><release>2026-02-28T00:00:00Z</release><modification>2026-02-28T02:02:24.619Z</modification><creation>2026-02-11T12:07:47.342Z</creation></dates><accession>E-MTAB-16640</accession><cross_references><ENA>ERP188994</ENA><EFO>EFO_0002944</EFO><EFO>EFO_0004170</EFO><EFO>EFO_0009653</EFO><EFO>EFO_0005518</EFO><EFO>EFO_0004184</EFO></cross_references></HashMap>