Published April 17, 2009 | Version v1
Journal article

Glucocorticoid receptor (GR) β has intrinsic, GRα-independent transcriptional activity

  • 1. Program in Reproductive and Adult Endocrinology, Eunice Kennedy Shriver National Institute of Child Health and Human Development, Bldg. 10, CRC, Rm. 1-3140, 10 Center Drive MSC 1109, Bethesda, MD 20892-1109 (United States)
  • 2. First Department of Pediatrics, Athens University Medical School (United States)
  • 3. Laboratory of Clinical Investigation, National Center for Complementary and Alternative Medicine (United States)
  • 4. Clinical Molecular Profiling Core, Advanced Technology Center, National Cancer Institute (United States)
  • 5. Department of Biochemistry and Molecular Biology, The Catherine Birch McCormick Genomics Center, George Washington University School of Medicine and Health Sciences (United States)

Description

The human glucocorticoid receptor (GR) gene produces C-terminal GRβ and GRα isoforms through alternative use of specific exons 9β and α, respectively. We explored the transcriptional activity of GRβ on endogenous genes by developing HeLa cells stably expressing EGFP-GRβ or EGFP. Microarray analyses revealed that GRβ had intrinsic gene-specific transcriptional activity, regulating mRNA expression of a large number of genes negatively or positively. Majority of GRβ-responsive genes was distinct from those modulated by GRα, while GRβ and GRα mutually modulated each other's transcriptional activity in a subpopulation of genes. We did not observe in HCT116 cells nuclear translocation of GRβ and activation of this receptor by RU 486, a synthetic steroid previously reported to bind GRβ and to induce nuclear translocation. Our results indicate that GRβ has intrinsic, GRα-independent, gene-specific transcriptional activity, in addition to its previously reported dominant negative effect on GRα-induced transactivation of GRE-driven promoters.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.bbrc.2009.02.110

Additional details

Identifiers

DOI
10.1016/j.bbrc.2009.02.110;
PII
S0006-291X(09)00394-5;

Publishing Information

Journal Title
Biochemical and Biophysical Research Communications
Journal Volume
381
Journal Issue
4
Journal Page Range
p. 671-675
ISSN
0006-291X
CODEN
BBRCA9

INIS

Country of Publication
United States
Country of Input or Organization
International Atomic Energy Agency (IAEA)
INIS RN
45020481
Subject category
S60: APPLIED LIFE SCIENCES;
Descriptors DEI
EXONS; GENES; GLUCOCORTICOIDS; HELA CELLS; MESSENGER-RNA; PROMOTERS; RECEPTORS; SPLICING; TRANSLOCATION
Descriptors DEC
ADRENAL HORMONES; ANIMAL CELLS; CORTICOSTEROIDS; HORMONES; HYDROXY COMPOUNDS; KETONES; MEMBRANE PROTEINS; NUCLEIC ACIDS; ORGANIC COMPOUNDS; PREGNANES; PROTEINS; RNA; RNA PROCESSING; STEROID HORMONES; STEROIDS; TUMOR CELLS

Optional Information

Copyright
Copyright (c) 2009 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.