Regulation of mRNA turnover in cystic fibrosis lung disease

Abstract

Cystic fibrosis (CF) is an autosomal recessive disease due to mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene, F508del‐CFTR being the most frequent mutation. The CF lung is characterized by a hyperinflammatory phenotype and is regulated by multiple factors that coordinate its pathophysiology. In CF the expression of CFTR as well as proinflammatory genes are regulated at the level of messenger RNA (mRNA) stability, which subsequently affect translation. These mechanisms are mediated by inflammatory RNA‐binding proteins as well as small endogenous noncoding microRNAs, in coordination with cellular signaling pathways. These regulatory factors exhibit altered expression and function in vivo in the CF lung, and play a key role in the pathophysiology of CF lung disease. In this review, we have described the role of mRNA stability and associated regulatory mechanisms in CF lung disease. WIREs RNA 2017, 8:e1408. doi: 10.1002/wrna.1408

Document Details

Document Type
Pub Defense Publication
Publication Date
Nov 13, 2016
Source ID
10.1002/wrna.1408

Entities

People

  • Harvey B. Pollard
  • Parameet Kumar
  • Roopa Biswas

Organizations

  • Cystic Fibrosis Foundation
  • Uniformed Services University of the Health Sciences

Tags

Fields of Study

  • Biology

Readers

  • Immunology and Pathology
  • Molecular Biology and Genetics
  • Molecular Genetics