Literature DB >> 20735177

Transcriptional regulation of energy metabolism in the liver.

Keiko Hirota1, Akiyoshi Fukamizu.   

Abstract

Living organisms maintain energy homeostasis by constantly adjusting internal metabolic activities in response to nutritional states. Energy metabolism is regulated by the quality and quantity of the enzymes that catalyze metabolic reactions. Recruitment and regulation of enzymes responsible for transcriptional control, among others, play an important role in this process. Located downstream from intracellular signaling cascades, transcription factors receive information signals from multiple sources. Their primary function is to integrate and interpret this information in terms of transcriptional output. It was recently suggested that signal content is converted via post-transcriptional modifications of the transcription factors. Many studies have shown that multiple signaling pathways converge on single transcription factors. This review discusses the post-translational modifications of transcription factors involved in the regulation of glucose metabolism, as well as the signaling networks in which they play a role.

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Year:  2010        PMID: 20735177     DOI: 10.3109/10799893.2010.509730

Source DB:  PubMed          Journal:  J Recept Signal Transduct Res        ISSN: 1079-9893            Impact factor:   2.092


  4 in total

Review 1.  Metabolic choreography of gene expression: nutrient transactions with the epigenome.

Authors:  Babukrishna Maniyadath; U S Sandra; Ullas Kolthur-Seetharam
Journal:  J Biosci       Date:  2020       Impact factor: 1.826

2.  Regulation of hepatocyte cell cycle re-entry by RNA polymerase II-associated Gdown1.

Authors:  Miki Jishage; Robert G Roeder
Journal:  Cell Cycle       Date:  2020-11-25       Impact factor: 4.534

3.  Contrasting Patterns in the Evolution of Vertebrate MLX Interacting Protein (MLXIP) and MLX Interacting Protein-Like (MLXIPL) Genes.

Authors:  Parmveer Singh; David M Irwin
Journal:  PLoS One       Date:  2016-02-24       Impact factor: 3.240

4.  Transcriptional down-regulation of metabolic genes by Gdown1 ablation induces quiescent cell re-entry into the cell cycle.

Authors:  Miki Jishage; Keiichi Ito; Chi-Shuen Chu; Xiaoling Wang; Masashi Yamaji; Robert G Roeder
Journal:  Genes Dev       Date:  2020-05-07       Impact factor: 11.361

  4 in total

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