MIR149
microRNA 149 | hsa-mir-149, MIRN149

microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]

Biological processes 25 terms
RISC complex (GO:0016442)cellular response to fibroblast growth factor stimulus (GO:0044344)cellular response to interleukin-6 (GO:0071354)mRNA base-pairing post-transcriptional repressor activity (GO:1903231)mRNA base-pairing post-transcriptional repressor activity (GO:1903231)miRNA-mediated gene silencing by mRNA destabilization (GO:0035279)miRNA-mediated post-transcriptional gene silencing (GO:0035195)miRNA-mediated post-transcriptional gene silencing (GO:0035195)miRNA-mediated post-transcriptional gene silencing (GO:0035195)negative regulation of blood vessel endothelial cell proliferation involved in sprouting angiogenesis (GO:1903588)negative regulation of cell migration (GO:0030336)negative regulation of cell migration involved in sprouting angiogenesis (GO:0090051)negative regulation of cell population proliferation (GO:0008285)negative regulation of endothelial cell chemotaxis to fibroblast growth factor (GO:2000545)negative regulation of epithelial to mesenchymal transition (GO:0010719)negative regulation of fibroblast growth factor receptor signaling pathway (GO:0040037)negative regulation of inflammatory response (GO:0050728)negative regulation of interleukin-6 production (GO:0032715)negative regulation of non-canonical NF-kappaB signal transduction (GO:1901223)negative regulation of receptor signaling pathway via STAT (GO:1904893)negative regulation of stress fiber assembly (GO:0051497)negative regulation of toll-like receptor 4 signaling pathway (GO:0034144)negative regulation of tumor necrosis factor production (GO:0032720)positive regulation of collagen biosynthetic process (GO:0032967)positive regulation of transforming growth factor beta3 production (GO:0032916)
Expression (TPM)
MIR149 — as a Regulated Gene

TFs regulating MIR149 0 TFs

Transcription factors with Perturb-seq knockdown data for MIR149. The Binding column indicates whether any binding evidence exists for this TF–gene pair (ChIP-seq or motif footprint peaks). The Mean coef is the average Perturb-seq regression coefficient across active gRNAs (positive = MIR149 upregulated upon KD; negative = downregulated). The Outlier column indicates whether this gene is in the top or bottom 5% of all TF knockdown effects.

Data: Effect:
TF Mean coef Binding Outlier TF→Gene link

Elements linked to MIR149

Open chromatin peaks (ATAC-seq) in the genomic neighbourhood of MIR149, linked by TSS proximity or chromatin conformation (Multiome / HiCAR). Each element overlaps at least one TF ChIP-seq binding site — the TFs column shows how many distinct TFs bind that element.

Accessibility Element Dist. to TSS Link type TFs
chr2:240,452,173–240,453,282 2.7 kb Proximal (<10kb) 285
chr2:240,455,722–240,456,136 at TSS At TSS 143

Genome Browser

Genomic view of the MIR149 locus showing ATAC-seq accessibility and RNA-seq expression across the ESC → DE time course, together with TF binding peaks and element-to-TSS loop connections.

chr2:240,442,173 – 240,466,136
Proximal 1 kb Distal 10 kb Multiome HiCAR ATAC-seq RNA-seq