Differential Expression of SWI/SNF Chromatin Remodeler Subunits Brahma and Brahma-Related Gene During Drug-Induced Liver Injury and Regeneration in Mouse Model
- PMID: 27097303
- DOI: 10.1089/dna.2015.3155
Differential Expression of SWI/SNF Chromatin Remodeler Subunits Brahma and Brahma-Related Gene During Drug-Induced Liver Injury and Regeneration in Mouse Model
Abstract
The chromatin remodeling activity of mammalian SWI/SNF complex is carried out by either Brahma (BRM) or Brahma-related gene (BRG-1). The BRG-1 regulates genes involved in cell proliferation, whereas BRM is associated with cell differentiation, and arrest of cell growth. Global modifications of histones and expression of genes of chromatin-remodeling subunits have not been studied in in vivo model systems. In the present study, we investigate epigenetic modifications of histones and the expression of genes in thioacetamide (TAA)-induced liver injury and regeneration in a mouse model. In the present study, we report that hepatocyte proliferation and H3S10 phosphorylation occur during 60 to 72 h post TAA treatment in mice. Furthermore, there was change in the H3K9 acetylation and H3K9 trimethylation pattern with respect to liver injury and regeneration phase. Looking into the expression pattern of Brg-1 and Brm, it is evident that they contribute substantially to the process of liver regeneration. The SWI/SNF remodeler might contain BRG-1 as its ATPase subunit during injury phase. Whereas, BRM-associated SWI/SNF remodeler might probably be predominant during decline of injury phase and initiation of regeneration phase. Furthermore, during the regeneration phase, BRG-1-containing remodeler again predominates. Considering all these observations, the present study depicts an interplay between chromatin interacting machineries in different phases of thioacetamide-induced liver injury and regeneration.
Similar articles
-
Roles of Brahma and Brahma/SWI2-related gene 1 in hypoxic induction of the erythropoietin gene.J Biol Chem. 2004 Nov 5;279(45):46733-41. doi: 10.1074/jbc.M409002200. Epub 2004 Sep 3. J Biol Chem. 2004. PMID: 15347669
-
Mammalian chromatin remodeling complex SWI/SNF is essential for enhanced expression of the albumin gene during liver development.J Biochem. 2006 Feb;139(2):177-88. doi: 10.1093/jb/mvj015. J Biochem. 2006. PMID: 16452305
-
An essential role for a mammalian SWI/SNF chromatin-remodeling complex during male meiosis.Development. 2012 Mar;139(6):1133-40. doi: 10.1242/dev.073478. Epub 2012 Feb 8. Development. 2012. PMID: 22318225 Free PMC article.
-
The SWI/SNF complex and cancer.Oncogene. 2009 Apr 9;28(14):1653-68. doi: 10.1038/onc.2009.4. Epub 2009 Feb 23. Oncogene. 2009. PMID: 19234488 Review.
-
The BRG1 ATPase of human SWI/SNF chromatin remodeling enzymes as a driver of cancer.Epigenomics. 2017 Jun;9(6):919-931. doi: 10.2217/epi-2017-0034. Epub 2017 May 19. Epigenomics. 2017. PMID: 28521512 Free PMC article. Review.
Cited by
-
ATP-dependent chromatin remodelers in ageing and age-related disorders.Biogerontology. 2021 Feb;22(1):1-17. doi: 10.1007/s10522-020-09899-3. Epub 2020 Sep 23. Biogerontology. 2021. PMID: 32968929 Review.
-
BRM: the core ATPase subunit of SWI/SNF chromatin-remodelling complex-a tumour suppressor or tumour-promoting factor?Epigenetics Chromatin. 2019 Nov 13;12(1):68. doi: 10.1186/s13072-019-0315-4. Epigenetics Chromatin. 2019. PMID: 31722744 Free PMC article. Review.
-
Opening and changing: mammalian SWI/SNF complexes in organ development and carcinogenesis.Open Biol. 2024 Oct;14(10):240039. doi: 10.1098/rsob.240039. Epub 2024 Oct 30. Open Biol. 2024. PMID: 39471843 Free PMC article. Review.
-
Trans-activation of eotaxin-1 by Brg1 contributes to liver regeneration.Cell Death Dis. 2022 May 25;13(5):495. doi: 10.1038/s41419-022-04944-0. Cell Death Dis. 2022. PMID: 35614068 Free PMC article.
-
Mechanism and Therapeutic Opportunities of Histone Modifications in Chronic Liver Disease.Front Pharmacol. 2021 Nov 23;12:784591. doi: 10.3389/fphar.2021.784591. eCollection 2021. Front Pharmacol. 2021. PMID: 34887768 Free PMC article. Review.
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Miscellaneous