AUTOREGULATION OF GLUCOCORTICOID RECEPTOR GENE-EXPRESSION

被引:141
作者
BURNSTEIN, KL
BELLINGHAM, DL
JEWELL, CM
POWELLOLIVER, FE
CIDLOWSKI, JA
机构
[1] UNIV N CAROLINA,DEPT PHYSIOL,CB 7545,460 MED SCI RES BLDG,CHAPEL HILL,NC 27599
[2] UNIV N CAROLINA,DEPT BIOCHEM,CHAPEL HILL,NC 27599
[3] UNIV N CAROLINA,LINEBERGER CANC RES CTR,CHAPEL HILL,NC 27599
关键词
GLUCOCORTICOID RECEPTOR; DOWN-REGULATION; STEROID HORMONE RECEPTOR; AUTOREGULATION;
D O I
10.1016/0039-128X(91)90124-E
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Glucocorticoid receptors are members of a highly conserved family of steroid receptor proteins, which are ligand-dependent transcription factors. Previous studies have shown that the presence of functional glucocorticoid receptors is a prerequisite for manifestation of cellular responses to hormone. Glucocorticoid receptors undergo down-regulation following treatment with glucocorticoids. To define the molecular mechanisms that are involved in this process we have analyzed the down-regulation of glucocorticoid receptors both in HeLa cells, which contain endogenous receptors, and in cells containing receptors that have been introduced by DNA transfection. Our results show that cells that contain contain glucocorticoid receptors-either endogenous or transfected-undergo down-regulation of steroid-binding capabilities, as well as reductions in receptor protein and mRNA levels, in a remarkably similar fashion. DNA sequences in the coding region of the human glucocorticoid receptor cDNA appear to be sufficient to account for down-regulation of receptor. This novel finding suggests that unique mechanisms are involved in controlling glucocorticoid receptor homeostasis.
引用
收藏
页码:52 / 58
页数:7
相关论文
共 45 条
  • [1] BADLEY JE, 1988, BIOTECHNIQUES, V6, P114
  • [2] Ballard P L, 1979, Monogr Endocrinol, V12, P493
  • [3] STABLE OVERPRODUCTION OF INTACT GLUCOCORTICOID RECEPTORS IN MAMMALIAN-CELLS USING A SELECTABLE GLUCOCORTICOID RESPONSIVE DIHYDROFOLATE-REDUCTASE GENE
    BELLINGHAM, DL
    CIDLOWSKI, JA
    [J]. MOLECULAR ENDOCRINOLOGY, 1989, 3 (11) : 1733 - 1747
  • [4] BLOOMFIELD CD, 1981, CANCER RES, V41, P4857
  • [5] BOURGEOIS S, 1979, CANCER RES, V39, P4749
  • [6] BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
  • [7] REGULATION OF GENE-EXPRESSION BY GLUCOCORTICOIDS
    BURNSTEIN, KL
    CIDLOWSKI, JA
    [J]. ANNUAL REVIEW OF PHYSIOLOGY, 1989, 51 : 683 - 699
  • [8] BURNSTEIN KL, 1990, J BIOL CHEM, V265, P7284
  • [9] ISOLATION OF BIOLOGICALLY-ACTIVE RIBONUCLEIC-ACID FROM SOURCES ENRICHED IN RIBONUCLEASE
    CHIRGWIN, JM
    PRZYBYLA, AE
    MACDONALD, RJ
    RUTTER, WJ
    [J]. BIOCHEMISTRY, 1979, 18 (24) : 5294 - 5299
  • [10] NOVEL ANTIPEPTIDE ANTIBODIES TO THE HUMAN GLUCOCORTICOID RECEPTOR - RECOGNITION OF MULTIPLE RECEPTOR FORMS INVITRO AND DISTINCT LOCALIZATION OF CYTOPLASMIC AND NUCLEAR RECEPTORS
    CIDLOWSKI, JA
    BELLINGHAM, DL
    POWELLOLIVER, FE
    LUBAHN, DB
    SAR, M
    [J]. MOLECULAR ENDOCRINOLOGY, 1990, 4 (10) : 1427 - 1437