Identification of a novel glucocorticoid response unit (GRU) in the 5′-flanking region of the mouse IL-2 receptor α gene

被引:12
作者
Lamas, M
Campos, JR
Silva, AG
机构
[1] CSIC, Ctr Invest Biol, Dept Inmunol, E-28006 Madrid, Spain
[2] CSIC, Ctr Invest Biol, Dept Biol Celular, E-28006 Madrid, Spain
关键词
IL-2; receptor; IL-2 receptor alpha gene regulation; glucocorticoid responsive unit; T cell transfection;
D O I
10.1006/cyto.1997.0248
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Glucocorticoid hormones inhibit the production of IL-2 and upregulate mouse interleukin 2 receptor alpha (IL-2R alpha) gene expression in T cell lines by increasing its transcription rate, Now, the authors have used functional approaches to search for regulatory elements present in the 5' flanking region of the IL-2R alpha gene responsible for this effect, An important regulatory region was detected between -1382 and -1100 bp from the transcription initiation site, Within this region the authors characterized two 20 bp long cis-acting regulatory elements, named G1 and G2, which are involved in the modulation of the expression of the IL-2R alpha gene by glucocorticoids, G1 contains a relatively well-conserved GRE half palindrome site, able to bind a partially purified glucocorticoid receptor but giving rise to an unstable complex, The G2 regulatory element contains no consensus sequences of binding sites for GR nor for any other described transcriptional factors but is able to form complexes with factors presents in liver or T cells, Whereas G1 or G2 alone were unable to induce a glucocorticoid-response, the contiguous presence of G1 and G2 gave rise to an efficient response, Therefore, it is postulated that the glucocorticoid-induction of IL-2R alpha gene is mediated, at least partly, through G1 and G2 elements which constitute a novel multicomponent glucocorticoid response unit (GRU). (C) 1997 Academic Press Limited.
引用
收藏
页码:973 / 981
页数:9
相关论文
共 36 条
[1]
INDUCTION OF HIGH-AFFINITY INTERLEUKIN-1 RECEPTOR ON HUMAN PERIPHERAL-BLOOD LYMPHOCYTES BY GLUCOCORTICOID HORMONES [J].
AKAHOSHI, T ;
OPPENHEIM, JJ ;
MATSUSHIMA, K .
JOURNAL OF EXPERIMENTAL MEDICINE, 1988, 167 (03) :924-936
[2]
ARYA SK, 1984, J IMMUNOL, V133, P273
[3]
THE IMMUNE-HYPOTHALAMIC-PITUITARY-ADRENAL AXIS [J].
BATEMAN, A ;
SINGH, A ;
KRAL, T ;
SOLOMON, S .
ENDOCRINE REVIEWS, 1989, 10 (01) :92-112
[4]
GENE-REGULATION BY STEROID-HORMONES [J].
BEATO, M .
CELL, 1989, 56 (03) :335-344
[5]
EFFICIENT BINDING OF GLUCOCORTICOID RECEPTOR TO ITS RESPONSIVE ELEMENT REQUIRES A DIMER AND DNA FLANKING SEQUENCES [J].
CHALEPAKIS, G ;
SCHAUER, M ;
CAO, XN ;
BEATO, M .
DNA AND CELL BIOLOGY, 1990, 9 (05) :355-368
[6]
THE IMMUNE-HYPOTHALAMO-PITUITARY-ADRENAL AXIS AND AUTOIMMUNITY [J].
DERIJK, R ;
BERKENBOSCH, F .
INTERNATIONAL JOURNAL OF NEUROSCIENCE, 1991, 59 (1-3) :91-100
[7]
TRANSCRIPTION FACTOR INTERACTIONS - SELECTORS OF POSITIVE OR NEGATIVE REGULATION FROM A SINGLE DNA ELEMENT [J].
DIAMOND, MI ;
MINER, JN ;
YOSHINAGA, SK ;
YAMAMOTO, KR .
SCIENCE, 1990, 249 (4974) :1266-1272
[8]
NOVEL GLUCOCORTICOID RECEPTOR COMPLEX WITH DNA ELEMENT OF THE HORMONE-REPRESSED POMC GENE [J].
DROUIN, J ;
SUN, YL ;
CHAMBERLAND, M ;
GAUTHIER, Y ;
DELEAN, A ;
NEMER, M ;
SCHMIDT, TJ .
EMBO JOURNAL, 1993, 12 (01) :145-156
[9]
HOMODIMER FORMATION IS RATE-LIMITING FOR HIGH-AFFINITY DNA-BINDING BY GLUCOCORTICOID RECEPTOR [J].
DROUIN, J ;
SUN, YL ;
TREMBLAY, S ;
LAVENDER, P ;
SCHMIDT, TJ ;
DELEAN, A ;
NEMER, M .
MOLECULAR ENDOCRINOLOGY, 1992, 6 (08) :1299-1309
[10]
ACTIVITY AND INTERLEUKIN-1 RESPONSIVENESS OF SV40 ENHANCER MOTIFS IN A RODENT IMMATURE T-CELL LINE [J].
ESPEL, E ;
FROMENTAL, C ;
REICHENBACH, P ;
NABHOLZ, M .
EMBO JOURNAL, 1990, 9 (03) :929-937