H19 Long Noncoding RNA Regulates Intestinal Epithelial Barrier Function via MicroRNA 675 by Interacting with RNA-Binding Protein HuR
Author(s) -
Tongtong Zou,
Suraj K. Jaladanki,
Lan Liu,
Lan Xiao,
Hee Kyoung Chung,
Junyao Wang,
Yan Xu,
Myriam Gorospe,
JianYing Wang
Publication year - 2016
Publication title -
molecular and cellular biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.14
H-Index - 327
eISSN - 1067-8824
pISSN - 0270-7306
DOI - 10.1128/mcb.01030-15
Subject(s) - adherens junction , biology , microrna , barrier function , rna binding protein , microbiology and biotechnology , tight junction , rna , translation (biology) , non coding rna , messenger rna , cadherin , intestinal mucosa , long non coding rna , gene , genetics , cell , medicine
The disruption of the intestinal epithelial barrier function occurs commonly in various pathologies, but the exact mechanisms responsible are unclear. TheH19 long noncoding RNA (lncRNA) regulates the expression of different genes and has been implicated in human genetic disorders and cancer. Here, we report thatH19 plays an important role in controlling the intestinal epithelial barrier function by serving as a precursor for microRNA 675 (miR-675).H19 overexpression increased the cellular abundance of miR-675, which in turn destabilized and repressed the translation of mRNAs encoding tight junction protein ZO-1 and adherens junction E-cadherin, resulting in the dysfunction of the epithelial barrier. Increasing the level of the RNA-binding protein HuR in cells overexpressingH19 prevented the stimulation of miR-675 processing fromH19 , promoted ZO-1 and E-cadherin expression, and restored the epithelial barrier function to a nearly normal level. In contrast, the targeted deletion of HuR in intestinal epithelial cells enhanced miR-675 production in the mucosa and delayed the recovery of the gut barrier function after exposure to mesenteric ischemia/reperfusion. These results indicate thatH19 interacts with HuR and regulates the intestinal epithelial barrier function via theH19 -encoded miR-675 by altering ZO-1 and E-cadherin expression posttranscriptionally.
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