Literature DB >> 12456302

Transcriptional regulation of the apolipoprotein AI gene.

Sohail Malik1.   

Abstract

Since the original description of the gene encoding apolipoprotein AI (apoAI) considerable progress has been made in identifying the regulatory regions and corresponding transcription factors that regulate its transcription in liver and intestinal cells. Nuclear receptors (in particular HNF-4) have emerged as the dominant (although by no means the exclusive) transcriptional activators that drive high levels of apoAI gene expression. In this review, some of the mechanisms (including interactions with recently described coactivators, as well as synergism with additional transcription factors bound to proximal and distal enhancers) that may underlie this process are discussed. Furthermore, apoAI gene expression has long been known to be subject to a variety of developmental, hormonal, dietary and pharmacological stimuli. The review thus also describes selected examples of these phenomena with the aim of highlighting how the operative transcriptional mechanisms are likely to be continually modified while maintaining the appropriate output.

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Year:  2003        PMID: 12456302     DOI: 10.2741/1005

Source DB:  PubMed          Journal:  Front Biosci        ISSN: 1093-4715


  7 in total

1.  Two functional modes of a nuclear receptor-recruited arginine methyltransferase in transcriptional activation.

Authors:  María J Barrero; Sohail Malik
Journal:  Mol Cell       Date:  2006-10-20       Impact factor: 17.970

2.  Type 1 Deiodinase Regulates ApoA-I Gene Expression and ApoA-I Synthesis Independent of Thyroid Hormone Signaling.

Authors:  Jing Liu; Antonio Hernandez-Ono; Mark J Graham; Valerie Anne Galton; Henry N Ginsberg
Journal:  Arterioscler Thromb Vasc Biol       Date:  2016-05-05       Impact factor: 8.311

3.  Activation of peroxisome proliferator activated receptor-gamma results in an atheroprotective apolipoprotein profile in HepG2 cells.

Authors:  Diala F Dahabreh; Jheem D Medh
Journal:  Adv Biol Chem       Date:  2012-08-22

4.  Enhanced hepatic apoA-I secretion and peripheral efflux of cholesterol and phospholipid in CD36 null mice.

Authors:  Pin Yue; Zhouji Chen; Fatiha Nassir; Carlos Bernal-Mizrachi; Brian Finck; Salman Azhar; Nada A Abumrad
Journal:  PLoS One       Date:  2010-03-26       Impact factor: 3.240

5.  Identification of DNA-dependent protein kinase as a cofactor for the forkhead transcription factor FoxA2.

Authors:  Adam Nock; Janice M Ascano; Tara Jones; Maria J Barrero; Naoyuki Sugiyama; Masaru Tomita; Yasushi Ishihama; Sohail Malik
Journal:  J Biol Chem       Date:  2009-05-28       Impact factor: 5.157

6.  The transcriptional activity of hepatocyte nuclear factor 4 alpha is inhibited via phosphorylation by ERK1/2.

Authors:  Borbála Vető; Dóra Bojcsuk; Caroline Bacquet; Judit Kiss; Szabolcs Sipeki; Ludovic Martin; László Buday; Bálint L Bálint; Tamás Arányi
Journal:  PLoS One       Date:  2017-02-14       Impact factor: 3.240

7.  Transcriptomic Analysis of Gonadal Adipose Tissue in Male Mice Exposed Perinatally to 2,2',4,4'-Tetrabromodiphenyl Ether (BDE-47).

Authors:  Aser Abrha; Alexander Suvorov
Journal:  Toxics       Date:  2018-03-29
  7 in total

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