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Thyroid hormone receptor and liver X receptor competitively up-regulate human selective Alzheimer's disease indicator-1 gene expression at the transcriptional levels.

Abstract
Selective Alzheimer's disease (AD) indicator-1 (Seladin-1) gene has been identified as a gene, whose expression is down-regulated in the vulnerable region in the brain of AD patients. Thyroid hormone (TH) is important to maintain the function of central nervous system and TH receptor (TR) is known to crosstalk with liver X receptor (LXR) on the lipid metabolism-related gene promoter. Recently, we have demonstrated that TR-β up-regulates the mouse Seladin-1 gene promoter at the transcriptional levels and LXR-α compensates the promoter activation only when the thyroid function is insufficient. In the current study, we have identified that TH and an LXR artificial agonist, TO901317 (TO) activated the human Seladin-1 promoter (-1024/+57 base pair (bp)) including consensus TH response element (TRE) half site (site A: -381 to -375 bp), and the site A mutation deteriorated the activation by TH and TO. Both TR-β and LXR-α heterodimerize with retinoid X receptor (RXR)-α on the site A, and chromatin immunoprecipitation (ChIP) assay revealed that TR-β, LXR-α and RXR-α are recruited to the site A. Moreover, TR-β and LXR-α functionally compete for the promoter activation in CV1 cells. Taken together, we concluded that TR-β and LXR-α competitively up-regulate the human Seladin-1 promoter, sharing the same response element, site A.
AuthorsEmi Ishida, Koshi Hashimoto, Shuichi Okada, Tetsurou Satoh, Masanobu Yamada, Masatomo Mori
JournalBiochemical and biophysical research communications (Biochem Biophys Res Commun) Vol. 432 Issue 3 Pg. 513-8 (Mar 15 2013) ISSN: 1090-2104 [Electronic] United States
PMID23416078 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
CopyrightCopyright © 2013 Elsevier Inc. All rights reserved.
Chemical References
  • Hydrocarbons, Fluorinated
  • Liver X Receptors
  • NR1H3 protein, human
  • Nerve Tissue Proteins
  • Nr1h3 protein, mouse
  • Orphan Nuclear Receptors
  • Sulfonamides
  • T0901317
  • Thyroid Hormone Receptors beta
  • Oxidoreductases Acting on CH-CH Group Donors
  • DHCR24 protein, human
Topics
  • Alzheimer Disease (genetics)
  • Base Sequence
  • Binding, Competitive
  • Cell Line, Tumor
  • Consensus Sequence
  • Gene Expression Regulation
  • Humans
  • Hydrocarbons, Fluorinated (pharmacology)
  • Liver X Receptors
  • Nerve Tissue Proteins (genetics)
  • Orphan Nuclear Receptors (agonists, metabolism)
  • Oxidoreductases Acting on CH-CH Group Donors (genetics)
  • Response Elements (drug effects, genetics)
  • Sulfonamides (pharmacology)
  • Thyroid Hormone Receptors beta (agonists, metabolism)
  • Transcription, Genetic
  • Up-Regulation

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