MINERALOCORTICOID AND GLUCOCORTICOID RECEPTOR ACTIVITIES DISTINGUISHED BY NONRECEPTOR FACTORS AT A COMPOSITE RESPONSE ELEMENT

被引:401
作者
PEARCE, D
YAMAMOTO, KR
机构
[1] UNIV CALIF SAN FRANCISCO, DEPT BIOCHEM & BIOPHYS, SAN FRANCISCO, CA 94143 USA
[2] UNIV CALIF SAN FRANCISCO, DIV NEPHROL, SAN FRANCISCO, CA 94143 USA
关键词
D O I
10.1126/science.8382376
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Mineralocorticoid and glucocorticoid hormones elicit distinct physiologic responses, yet the mineralocorticoid receptor (MR) and glucocorticoid receptor (GR) bind to and activate transcription similarly from a consensus simple hormone response element (HRE). The activities of GR and MR at plfG, a 25-base pair composite response element to which both the steroid receptors and transcription factor AP1 can bind, are analyzed here. Under conditions in which GR represses AP1-stimulated transcription from plfG, MR was inactive. With the use of MR-GR chimeras, a segment of the NH2-terminal region of GR (amino acids 105 to 440) was shown to be required for this repression. Thus, the distinct physiologic effects mediated by MR and GR may be determined by differential interactions of nonreceptor factors with specific receptor domains at composite response elements.
引用
收藏
页码:1161 / 1165
页数:5
相关论文
共 42 条
  • [1] ADLER AA, IN PRESS P NATL ACAD
  • [2] THE ORIGIN OF NUCLEAR RECEPTOR PROTEINS - A SINGLE PRECURSOR DISTINCT FROM OTHER TRANSCRIPTION FACTORS
    AMERO, SA
    KRETSINGER, RH
    MONCRIEF, ND
    YAMAMOTO, KR
    PEARSON, WR
    [J]. MOLECULAR ENDOCRINOLOGY, 1992, 6 (01) : 3 - 7
  • [3] CLONING OF HUMAN MINERALOCORTICOID RECEPTOR COMPLEMENTARY-DNA - STRUCTURAL AND FUNCTIONAL KINSHIP WITH THE GLUCOCORTICOID RECEPTOR
    ARRIZA, JL
    WEINBERGER, C
    CERELLI, G
    GLASER, TM
    HANDELIN, BL
    HOUSMAN, DE
    EVANS, RM
    [J]. SCIENCE, 1987, 237 (4812) : 268 - 275
  • [4] LOW-DOSE GLUCOCORTICOIDS STIMULATE ELECTRONEUTRAL NACL ABSORPTION IN RAT COLON
    BASTL, CP
    SCHULMAN, G
    CRAGOE, EJ
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY, 1989, 257 (06): : F1027 - F1038
  • [5] DNA-SEQUENCES BOUND SPECIFICALLY BY GLUCOCORTICOID RECEPTOR INVITRO RENDER A HETEROLOGOUS PROMOTER HORMONE RESPONSIVE INVIVO
    CHANDLER, VL
    MALER, BA
    YAMAMOTO, KR
    [J]. CELL, 1983, 33 (02) : 489 - 499
  • [6] JUN-B DIFFERS IN ITS BIOLOGICAL PROPERTIES FROM, AND IS A NEGATIVE REGULATOR OF, C-JUN
    CHIU, R
    ANGEL, P
    KARIN, M
    [J]. CELL, 1989, 59 (06) : 979 - 986
  • [7] COHEN DR, 1990, ONCOGENE, V5, P929
  • [8] TRANSCRIPTIONAL CONTROL OF C-JUN BY RETINOIC ACID
    DEGROOT, RP
    PALS, C
    KRUIJER, W
    [J]. NUCLEIC ACIDS RESEARCH, 1991, 19 (07) : 1585 - 1591
  • [9] TRANSCRIPTION FACTOR INTERACTIONS - SELECTORS OF POSITIVE OR NEGATIVE REGULATION FROM A SINGLE DNA ELEMENT
    DIAMOND, MI
    MINER, JN
    YOSHINAGA, SK
    YAMAMOTO, KR
    [J]. SCIENCE, 1990, 249 (4974) : 1266 - 1272
  • [10] LOCALIZATION OF 11-BETA-HYDROXYSTEROID DEHYDROGENASE TISSUE SPECIFIC PROTECTOR OF THE MINERALOCORTICOID RECEPTOR
    EDWARDS, CRW
    BURT, D
    MCINTYRE, MA
    DEKLOET, ER
    STEWART, PM
    BRETT, L
    SUTANTO, WS
    MONDER, C
    [J]. LANCET, 1988, 2 (8618) : 986 - 989