The Sp transcription factors are involved in the cellular expression of the human glucose-dependent insulinotropic polypeptide receptor gene and overexpressed in adrenals of patients with Cushing's syndrome

J Mol Endocrinol. 2005 Aug;35(1):61-71. doi: 10.1677/jme.1.01765.

Abstract

The best characterized effect of glucose-dependent insulinotropic polypeptide (GIP) is its stimulatory effect on insulin secretion by pancreatic beta-cells. Recently, it was demonstrated that some cases of primary adrenal Cushing's syndrome were secondary to the ectopic expression of non-mutated GIP receptor (GIP-R) in bilateral adrenal hyperplasias or unilateral adrenal adenomas, resulting in food-dependent steroidogenesis. Using a human multiple-expression tissue array, GIP-R was found to be expressed in a large number of human adult and fetal tissues, but not in the adrenal gland. The analysis of the promoter region of human (h) GIP-R gene revealed six consensus sequences important in regulating the reporter gene activity and capable of binding to Sp1 and Sp3 transcription factors. Data obtained by gene array and semi-quantitative RT-PCR showed an increase in the expression of Sp3 and CRSP9 (co-regulator of Sp1 transcription factor, subunit 9) in the adrenal adenomas or bilateral macronodular hyperplasias of patients with GIP-dependent Cushing's syndrome; they were, however, also increased in some patients with non-GIP-dependent cortisol-secreting adenomas or with ACTH-dependent Cushing's disease. This study represents the first step in our understanding of the mechanisms involved in the regulation of the expression of the hGIP-R gene.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adrenal Glands / metabolism*
  • Adult
  • Base Sequence
  • Binding Sites / genetics
  • Case-Control Studies
  • Consensus Sequence
  • Cushing Syndrome / genetics*
  • Cushing Syndrome / metabolism*
  • DNA / genetics
  • DNA / metabolism
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / metabolism*
  • Fetus / metabolism
  • Gene Expression
  • Genes, Reporter
  • Humans
  • Mediator Complex
  • Molecular Sequence Data
  • Promoter Regions, Genetic
  • Receptors, Gastrointestinal Hormone / genetics*
  • Sp1 Transcription Factor / genetics
  • Sp1 Transcription Factor / metabolism*
  • Sp3 Transcription Factor
  • Tissue Distribution
  • Trans-Activators / genetics
  • Trans-Activators / metabolism
  • Transcription Factors / genetics
  • Transcription Factors / metabolism*
  • Transfection

Substances

  • DNA-Binding Proteins
  • MED7 protein, human
  • Mediator Complex
  • Receptors, Gastrointestinal Hormone
  • SP3 protein, human
  • Sp1 Transcription Factor
  • Trans-Activators
  • Transcription Factors
  • Sp3 Transcription Factor
  • DNA
  • gastric inhibitory polypeptide receptor