<HashMap><database>ENA</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR866/003/SRR8662713/SRR8662713_2.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR866/004/SRR8662714/SRR8662714_1.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR866/003/SRR8662713/SRR8662713_1.fastq.gz</Fastqsanger.gz><Fastqsanger.gz>ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR866/004/SRR8662714/SRR8662714_2.fastq.gz</Fastqsanger.gz></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Genomics</omics_type><center_name>immunology, PUMC</center_name><full_dataset_link>https://www.ebi.ac.uk/ena/browser/view/PRJNA525363</full_dataset_link><scientific_name>Mus musculus</scientific_name><long_description>To identify new target genes of miR-1, the affinity based purification experiments of mouse mRNAs using biotin-labeled miR-1 as probes was performed in peritoneal macorphages. Enriched RNAs and input samples were then subjected to RNA sequencing using an Illumina platform. Overall design: To de novo explore miR-1 target genes in peritnoeal macrophage cells, we performed a modified miRIP protocol using biotin-labeled miR-1 as oligo nucleotide probes to in vivo affinity purify the genes using nucleic acid hybridization and use Illumina Next Generation Sequencing assay to identify the associated RNAs.</long_description><repository>ENA</repository><description_synonyms>biochemical pathways, macrophagocyte, single-organism catabolic process, multicellular organismal catabolic process, cellular breakdown, RNA, degradation, Monocyte Derived Macrophages, Polyadenylated, STAT91, typical plasmatocyte, Messenger RNA, IFNA@, Monocyte Derived, XStat1, monocyte-derived macrophage, cellular catabolism, DD6G4-4, IFNA13, Monocyte-Derived, Non-Polyadenylated mRNA., macrophage, ISGF-3, Messenger, Poly(A)+ mRNA, responsivity, Monocyte-Derived Macrophage, INSDC_feature:mRNA, cellular degradation, Signal transducer and activator of transcription 1-alpha/beta, secretion, Polyadenylated RNA, agranular plasmatocyte, Non Polyadenylated, breakdown of molecule, Monocyte-Derived Macrophages, Macrophage, Polyadenylated Messenger RNA, reactivity, Poly(A)+ RNA, Non Polyadenylated mRNA, breakdown, CANDF7, protein_coding_transcript, biodegradation, IFN-alphaD, mRNA, Poly(A) Tail, breakdown of chemical, catabolism, Macrophages, 2010005J02Rik, IFL, Polyadenylated Messenger, IFN, Non-Polyadenylated, messenger RNA, Bone Marrow Derived Macrophages, Bone Marrow-Derived Macrophage, Bone Marrow-Derived, breakdown of substance, template RNA, STAT1, lamellocyte, IMD31B, IMD31C, IMD31A, Bone Marrow-Derived Macrophages, AA408197, granulocyte, biotransformation, histiocyte, response, Polyadenylated mRNA, transcription factor ISGF-3 components p91/p84, Poly(A) RNA, IFN-ALPHA</description_synonyms><name_synonyms>biochemical pathways, macrophagocyte, single-organism catabolic process, multicellular organismal catabolic process, cellular breakdown, RNA, degradation, Monocyte Derived Macrophages, Polyadenylated, STAT91, typical plasmatocyte, Messenger RNA, IFNA@, Monocyte Derived, XStat1, monocyte-derived macrophage, cellular catabolism, DD6G4-4, IFNA13, Monocyte-Derived, Non-Polyadenylated mRNA., macrophage, ISGF-3, Messenger, Poly(A)+ mRNA, responsivity, Monocyte-Derived Macrophage, INSDC_feature:mRNA, cellular degradation, Signal transducer and activator of transcription 1-alpha/beta, secretion, Polyadenylated RNA, agranular plasmatocyte, Non Polyadenylated, breakdown of molecule, Monocyte-Derived Macrophages, Macrophage, Polyadenylated Messenger RNA, reactivity, Poly(A)+ RNA, Non Polyadenylated mRNA, breakdown, CANDF7, protein_coding_transcript, biodegradation, IFN-alphaD, mRNA, Poly(A) Tail, breakdown of chemical, catabolism, Macrophages, 2010005J02Rik, IFL, Polyadenylated Messenger, IFN, Non-Polyadenylated, messenger RNA, Bone Marrow Derived Macrophages, Bone Marrow-Derived Macrophage, Bone Marrow-Derived, breakdown of substance, template RNA, STAT1, lamellocyte, IMD31B, IMD31C, IMD31A, Bone Marrow-Derived Macrophages, AA408197, granulocyte, biotransformation, histiocyte, response, Polyadenylated mRNA, transcription factor ISGF-3 components p91/p84, Poly(A) RNA, IFN-ALPHA</name_synonyms></additional><is_claimable>false</is_claimable><name>Inducible degradation of Sros1 promotes IFN-γ-activated macrophage innate response by stabilizing STAT1 mRNA</name><description>Inducible degradation of Sros1 promotes IFN-γ-activated macrophage innate response by stabilizing STAT1 mRNA</description><dates><last_updated>2025-09-24</last_updated><first_public>2019-09-20</first_public></dates><accession>PRJNA525363</accession><cross_references><GEO>GSE127769</GEO><taxon>10090</taxon></cross_references></HashMap>