Literature DB >> 27621183

BRD4 regulates fructose-inducible lipid accumulation-related genes in the mouse liver.

Aki Yamada1, Kazue Honma1, Kazuki Mochizuki2, Toshinao Goda3.   

Abstract

OBJECTIVE: Fructose intake induces hepatic steatosis by activating fat synthesis. In this study, we searched for genes that showed acute induction in the livers of mice force-fed with fructose, and examined how this induction is regulated. MATERIALS/
METHODS: We identified genes induced at 6h after the fructose force-feeding using a microarray and quantitative real-time RT-PCR. Histone acetylation and an acetylated histone binding protein bromodomain containing (BRD)4 binding around the fructose-inducible genes were examined using a chromatin immunoprecipitation assay. We examined whether (+)-JQ1, an inhibitor of the binding between the BRD4 and acetylated histones, inhibited the expressions of fructose-inducible genes, histone acetylation and BRD4 binding around the genes.
RESULTS: We identified upregulated genes related to lipid accumulation, such as Cyp8b1, Dak and Plin5, in mice force-fed with fructose compared with those force-fed with glucose. Acetylation of histones H3 and H4, and BRD4 binding around the transcribed region of those fructose-inducible genes, were enhanced by fructose force-feeding. Meanwhile, (+)-JQ1 treatment reduced expressions of fructose-inducible genes, histone acetylation and BRD4 binding around these genes.
CONCLUSIONS: Acute induction of genes related to lipid accumulation in the livers of mice force-fed with fructose is associated with the induction of histone acetylation and BRD4 binding around these genes.
Copyright © 2016 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  BRD4; Fructose; Histone acetylation; Lipid metabolism; Liver

Mesh:

Substances:

Year:  2016        PMID: 27621183     DOI: 10.1016/j.metabol.2016.07.001

Source DB:  PubMed          Journal:  Metabolism        ISSN: 0026-0495            Impact factor:   8.694


  7 in total

1.  Glucose-6-Phosphate Regulates Hepatic Bile Acid Synthesis in Mice.

Authors:  Joanne A Hoogerland; Yu Lei; Justina C Wolters; Jan Freark de Boer; Trijnie Bos; Aycha Bleeker; Niels L Mulder; Theo H van Dijk; Jan A Kuivenhoven; Fabienne Rajas; Gilles Mithieux; Rebecca A Haeusler; Henkjan J Verkade; Vincent W Bloks; Folkert Kuipers; Maaike H Oosterveer
Journal:  Hepatology       Date:  2019-06-24       Impact factor: 17.425

2.  Bromodomain Protein BRD4 Accelerates Glucocorticoid Dysregulation of Bone Mass and Marrow Adiposis by Modulating H3K9 and Foxp1.

Authors:  Feng-Sheng Wang; Yu-Shan Chen; Jih-Yang Ko; Chung-Wen Kuo; Huei-Jing Ke; Chin-Kuei Hsieh; Shao-Yu Wang; Pei-Chen Kuo; Holger Jahr; Wei-Shiung Lian
Journal:  Cells       Date:  2020-06-19       Impact factor: 6.600

Review 3.  Plin5 Bidirectionally Regulates Lipid Metabolism in Oxidative Tissues.

Authors:  Xinqing Zhang; Wu Xu; Rui Xu; Zhen Wang; Xinyan Zhang; Peng Wang; Ke Peng; Meiling Li; Jing Li; Yanfei Tan; Xiong Wang; Haifeng Pei
Journal:  Oxid Med Cell Longev       Date:  2022-03-31       Impact factor: 6.543

Review 4.  Roles of Bromodomain Extra Terminal Proteins in Metabolic Signaling and Diseases.

Authors:  Dayu Wu; Qiong Duan
Journal:  Pharmaceuticals (Basel)       Date:  2022-08-22

Review 5.  Therapeutic targets, novel drugs, and delivery systems for diabetes associated NAFLD and liver fibrosis.

Authors:  Virender Kumar; Xiaofei Xin; Jingyi Ma; Chalet Tan; Natalia Osna; Ram I Mahato
Journal:  Adv Drug Deliv Rev       Date:  2021-07-24       Impact factor: 17.873

6.  Plasticity of histone modifications around Cidea and Cidec genes with secondary bile in the amelioration of developmentally-programmed hepatic steatosis.

Authors:  Jeenat Ferdous Urmi; Hiroaki Itoh; Keiko Muramatsu-Kato; Yukiko Kohmura-Kobayashi; Natsuyo Hariya; Divyanu Jain; Naoaki Tamura; Toshiyuki Uchida; Kazunao Suzuki; Yoshihiro Ogawa; Nobuaki Shiraki; Kazuki Mochizuki; Takeo Kubota; Naohiro Kanayama
Journal:  Sci Rep       Date:  2019-11-19       Impact factor: 4.379

Review 7.  Regulation of Carbohydrate-Responsive Metabolic Genes by Histone Acetylation and the Acetylated Histone Reader BRD4 in the Gene Body Region.

Authors:  Kazuki Mochizuki; Shiori Ishiyama; Natsuyo Hariya; Toshinao Goda
Journal:  Front Mol Biosci       Date:  2021-07-15
  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.