five

Genome-wide RELA binding sites in response to 5 microbial stimuli in Detroit562 cells [ChIP-seq]

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NIAID Data Ecosystem2026-03-11 收录
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https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE91018
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NFKB is a family of transcription factors (TF), which are master regulators of the innate immune system. It is activated downstream of pathogen recognition receptors after ligand binding and regulates the expression of antimicrobials, cytokines and chemokines, thus helping to fight infections as well as recruiting the adaptive immune system. Although NFKB responds to a wide variety of signals, the processes in which stimulus-specificity is attained are still unclear. Here, we characterized the response of one of the NFKB members, RELA, to five stimuli mimicking infection in nasopharyngeal epithelial cells. When comparing RELA genome-wide binding sites , we detected most of them to be overlapping among the different stimulations. Yet, we distinguished a minority of stimulus-specific RELA binding sites. Interestingly, some of these seemed to have a biological effect as they correlated with corresponding gene expression. Specifically, the response to Poly I:C mimicking viral dsRNA gave a distinct RELA profile binding the vicinity of antiviral genes. This group of binding sites was also enriched in Interferon Regulatory Factor motifs indicating that the interaction with more specialized TFs could contribute to stimulus-specific RELA activity. Furthermore, motif analysis revealed differences in the sequence of the NFKB motifs between certain stimulus-specific sets of peaks suggesting preferences for particular NFKB dimers in response to defined signals. Treatment of Detroit 562 cells with 5 stimuli: LPS, TNFα, Pam2CSK4, Poly I:C or M tri-DAP. Examination of RELA genome-wide binding sites by ChIP-seq after the 5 stimulations. Two biological duplicates were analyzed for each condition. Please note that the 'Input' and 'No Treatment' samples were used as background to call the peaks and generate the wig files for the processed data of Treatment RELA ChIP-seq (each treatment RELA ChIP-seq samples was processed against Input DNA + No Treatment RELA ChIP-seq (of the same batch) so the wig files generated are normalized ).
创建时间:
2019-05-29
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