Transcriptomic studies of mouse naïve and Th17 cell from wildtype or Malat1 deficient background. Transcriptomic studies of mouse naïve and Th17 cell from wildtype or Malat1 deficient background

Long non-coding RNAs (lncRNAs) are critical regulators of mammalian gene programs. Metastasis Associated Lung Adenocarcinoma Transcript 1 (Malat1) is the most abundant lncRNA expressed in intestinal Th17 cells critical for maintaining tissue homeostasis and regulating local inflammation. Here, we report that Malat1 negatively regulates IL-17A and IL-17F productions in intestinal Th17 cells during colitis and contributes to local inflammation. Global RNA interactions with DNA by deep sequencing (GRID-seq) coupled with transcriptomic studies revealed Malat1 is recruited to the Il17a-Il17f super enhancer in Th17 cells, and regulates Il17a-Il17f transcription. Overall design: Two independent biological replicates of Th17 cells were performed. The wild type samples are GSM4770961 and GSM4770962.