Regulation of Intestinal Epithelial Barrier Function by Long Noncoding RNA through Interaction with MicroRNA 29b.

The mammalian intestinal epithelium establishes a selectively permeable barrier that supports nutrient absorption and prevents intrusion by noxious luminal substances and microbiota. The effectiveness and integrity of the barrier function are tightly regulated via well-controlled mechanisms. Long noncoding RNAs transcribed from ultraconserved regions (T-UCRs) control diverse cellular processes, but their roles in the regulation of gut permeability remain largely unknown. Here we report that the T-UCR enhances intestinal epithelial barrier function by antagonizing microRNA 29b (miR-29b). Decreasing the levels of by gene silencing led to dysfunction of the intestinal epithelial barrier in cultured cells and increased the vulnerability of the gut barrier to septic stress in mice. specifically stimulated translation of the tight junction (TJ) claudin-1 (CLDN1) by associating with miR-29b rather than by binding directly to mRNA. acted as a natural decoy RNA for miR-29b, which interacts with mRNA via the 3' untranslated region and represses its translation. Ectopically expressed abolished the association of miR-29b with mRNA and restored claudin-1 expression to normal levels in cells overexpressing miR-29b, thus rescuing the barrier function. These results highlight a novel function of in controlling gut permeability and define a mechanism by which stimulates claudin-1 translation, by decreasing the availability of miR-29b to mRNA.