Title of article :
Epigenetics and Chromatin Remodeling Play a Role in Lung Disease
Author/Authors :
Mortaz، Esmaeil نويسنده Assistant to Editor-in-Chief , , Masjedi، Mohammad-Reza نويسنده , , Barnes، Peter J. نويسنده Department of Thoracic Medicine, National Heart & Lung Institute, Imperial College, London, United Kingdom , , Adcock، Ian M نويسنده Cell and Molecular Biology Group, Airways Disease Section, National Heart and Lung Institute, Imperial College London, UK ,
Issue Information :
فصلنامه با شماره پیاپی 0 سال 2011
Abstract :
Epigenetics is defined as heritable changes that affect gene expression without
altering the DNA sequence. Epigenetic regulation of gene expression is
facilitated through different mechanisms such as DNA methylation, histone
modifications and RNA-associated silencing by small non-coding RNAs. All
these mechanisms are crucial for normal development, differentiation and
tissue-specific gene expression. These three systems interact and stabilize one
another and can initiate and sustain epigenetic silencing, thus determining
heritable changes in gene expression. Histone acetylation regulates diverse
cellular functions including inflammatory gene expression, DNA repair and cell
proliferation. Transcriptional coactivators possess intrinsic histone
acetyltransferase activity and this activity drives inflammatory gene expression.
Eleven classical histone deacetylases (HDACs) act to regulate the expression of
distinct subsets of inflammatory/immune genes. Thus, loss of HDAC activity
or the presence of HDAC inhibitors can further enhance inflammatory gene
expression by producing a gene-specific change in HAT activity. For example,
HDAC2 expression and activity are reduced in lung macrophages, biopsy
specimens, and blood cells from patients with severe asthma and smoking
asthmatics, as well as in patients with chronic obstructive pulmonary disease
(COPD). This may account, at least in part, for the enhanced inflammation and
reduced steroid responsiveness seen in these patients. Other proteins,
particularly transcription factors, are also acetylated and are targets for
deacetylation by HDACs and sirtuins, a related family of 7 predominantly
protein deacetylases. Thus the acetylation/deacetylation status of NF-?B and
the glucocorticoid receptor can also affect the overall expression pattern of
inflammatory genes and regulate the inflammatory response. Understanding
and targeting specific enzymes involved in this process might lead to new
therapeutic agents, particularly in situations in which current antiinflammatory
therapies are suboptimal.
Journal title :
Tanaffos (Respiration)
Journal title :
Tanaffos (Respiration)