<HashMap><database>biostudies-arrayexpress</database><scores/><additional><submitter>Ya Chun Yu</submitter><organism>Mus musculus</organism><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/E-MTAB-16196</full_dataset_link><description>The aim of this study is to profile the distribution of the active histone modification H3K4me3 in BMDMs from WT and SLC1A5_var transgenic mice after low-dose LPS training. We compared the data of ChIP-seq performed on fragmented chromatin immunoprecipitated with anti-H3K4me3 antibody in naive and trained BMDM from both genotypes. Inter-group comparisons revealed increased differentially enriched peaks near promoters of pro-inflammatory genes of trained WT BMDMs, where as this changes were blunted in Tg BMDMs. Since SLC1A5_var function as unique mitochondrial glutamine transporter, the results indicate that altered glutaminolysis could impact epigenetic regulation under LPS-training,</description><repository>biostudies-arrayexpress</repository><sample_protocol>Library Construction - Purified DNA was subjected to library construction using the NEBNext® UltraTM DNA Library Prep Kit for Illumina (New England Biolabs). In brief, the chipped DNA was ligated with adaptors for PCR with index primers for multiplexing sequencing.</sample_protocol><sample_protocol>Sample Collection - BMDM form both of WT and SLC1A5_var were trained with PBS or LPS overnight. Cells were washed and rested until day 6 and harvested.</sample_protocol><sample_protocol>Nucleic Acid Extraction - Approximately 5 × 106 BMDMs were fixed, and the nuclei were collected, after which the chromatin was isolated and immunoprecipitated using an anti-histone H3 (trimethylated K4) antibody (Abcam) and a high-sensitivity ChIP kit (Abcam) according to the manufacturer’s instructions.</sample_protocol><sample_protocol>Sequencing - High-throughput sequencing was performed as paired-end 150-bp sequencing using NovaSeq X Plus (Illumina).</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><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><instrument_platform>Illumina NovaSeq X</instrument_platform><study_type>ChIP-seq</study_type><species>Mus musculus</species><pubmed_title>Mitochondrial Glutaminolysis Governs the Epigenetic Training of Macrophages for Antitumor Immunity.</pubmed_title><pubmed_authors>Ya Chun Yu, Yulseung Sung, Seonghun Lim, Jeoung Ah Kwon, Kuglae Kim, Do Sik Min, Hee Chan Yoo, Jung Min Han</pubmed_authors><pubmed_authors>Jung Min Han</pubmed_authors><pubmed_authors>Ya Chun Yu</pubmed_authors></additional><is_claimable>false</is_claimable><name>ChIP-seq analysis of LPS trained BMDMs  reveals remodeling of Histone 3 Lysine 4 tri-methylation (H3K4me3)</name><description>The aim of this study is to profile the distribution of the active histone modification H3K4me3 in BMDMs from WT and SLC1A5_var transgenic mice after low-dose LPS training. We compared the data of ChIP-seq performed on fragmented chromatin immunoprecipitated with anti-H3K4me3 antibody in naive and trained BMDM from both genotypes. Inter-group comparisons revealed increased differentially enriched peaks near promoters of pro-inflammatory genes of trained WT BMDMs, where as this changes were blunted in Tg BMDMs. Since SLC1A5_var function as unique mitochondrial glutamine transporter, the results indicate that altered glutaminolysis could impact epigenetic regulation under LPS-training,</description><dates><release>2026-06-24T00:00:00Z</release><modification>2026-06-24T03:04:00.41Z</modification><creation>2025-11-19T11:38:57.708Z</creation></dates><accession>E-MTAB-16196</accession><cross_references><ENA>ERP191643</ENA><EFO>EFO_0002944</EFO><EFO>EFO_0004170</EFO><EFO>EFO_0002692</EFO><EFO>EFO_0005518</EFO><EFO>EFO_0004184</EFO></cross_references></HashMap>