The activity of the human interleukin-5 conserved lymphokine element 0 is regulated by octamer factors in human cells

被引:25
作者
Thomas, MA
Mordvinov, VA
Sanderson, CJ
机构
[1] TVWT Inst Child Hlth Res, W Perth, Australia
[2] Curtin Univ Technol, Sch Biomed Sci, Perth, WA 6001, Australia
来源
EUROPEAN JOURNAL OF BIOCHEMISTRY | 1999年 / 265卷 / 01期
关键词
CLEO; gene expression; interleukin-5; octamer factors; regulation;
D O I
10.1046/j.1432-1327.1999.00732.x
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
Interleukin-5 (IL-5) controls the development of eosinophilia and contributes to a number of disease states including asthma. Expression of IL-5 is inducible under tight transcriptional regulation. This requires the contribution of several promoter elements; however, the conserved lymphokine element 0 (CLE0) in particular, is essential for expression of IL-5. In this study, we report the nuclear factors which regulate human IL-5 CLE0 activity in the human cell line PER-117. Using specific antibodies, we identified the transcriptional factors Oct-1 and Oct-2 binding to the 5' region of the CLE0 element. The involvement of Oct factors with CLE0 has not been reported previously in any of the lymphokines. In addition, the CLE0 element also appeared to complex with the transcriptional activator AP-1, consisting of the family members Jun D and Fra-2. We observed the binding of Oct-1 to be constitutive in comparison to Oct-2 and AP-1, both of which were induced in response to cell activation by PMA/A23187. Although the interaction of all three factors with CLE0 was closely linked and overlapping, residues critical to their binding were identified. We demonstrate, using site-directed mutagenesis and cotransfection experiments, that the CLE0 element is indispensable for IL-5 promoter activity and that Octamer factors contribute to the positive regulation of the hIL-5 gene.
引用
收藏
页码:300 / 307
页数:8
相关论文
共 43 条
[11]  
KARLEN S, 1996, BLOOD, V88, P210
[12]   PER-117 - A NEW HUMAN ALL CELL-LINE WITH AN IMMATURE THYMIC PHENOTYPE [J].
KEES, UR ;
FORD, J ;
PRICE, PJ ;
MEYER, BF ;
HERRMANN, RP .
LEUKEMIA RESEARCH, 1987, 11 (05) :489-+
[13]   DEGRADATION OF G(11)ALPHA/G(Q)ALPHA IS ACCELERATED BY AGONIST OCCUPANCY OF ALPHA(1A/D), ALPHA(1B), AND ALPHA(1C) ADRENERGIC-RECEPTORS [J].
WISE, A ;
LEE, TW ;
MACEWAN, DJ ;
MILLIGAN, G .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (29) :17196-17203
[14]  
Lee HJ, 1998, J IMMUNOL, V160, P2343
[15]   RECOMBINANT HUMAN INTERLEUKIN-5 IS A SELECTIVE ACTIVATOR OF HUMAN EOSINOPHIL FUNCTION [J].
LOPEZ, AF ;
SANDERSON, CJ ;
GAMBLE, JR ;
CAMPBELL, HD ;
YOUNG, IG ;
VADAS, MA .
JOURNAL OF EXPERIMENTAL MEDICINE, 1988, 167 (01) :219-224
[16]   A KERATINOCYTE-SPECIFIC TRANSCRIPTION FACTOR, KRF-1, INTERACTS WITH AP-1 TO ACTIVATE EXPRESSION OF HUMAN PAPILLOMAVIRUS TYPE-18 IN SQUAMOUS EPITHELIAL-CELLS [J].
MACK, DH ;
LAIMINS, LA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (20) :9102-9106
[17]   THE GRANULOCYTE-MACROPHAGE COLONY-STIMULATING FACTOR PROMOTER CIS-ACTING ELEMENT CLE0 MEDIATES INDUCTION SIGNALS IN T-CELLS AND IS RECOGNIZED BY FACTORS RELATED TO AP1 AND NFAT [J].
MASUDA, ES ;
TOKUMITSU, H ;
TSUBOI, A ;
SHLOMAI, J ;
HUNG, P ;
ARAI, KI ;
ARAI, N .
MOLECULAR AND CELLULAR BIOLOGY, 1993, 13 (12) :7399-7407
[18]   IL-5 PRODUCTION BY CD4(+) T-CELLS OF ASTHMATIC-PATIENTS IS SUPPRESSED BY GLUCOCORTICOIDS AND THE IMMUNOSUPPRESSANTS FK506 AND CYCLOSPORINE-A [J].
MORI, A ;
SUKO, M ;
NISHIZAKI, Y ;
KAMINUMA, O ;
KOBAYASHI, S ;
MATSUZAKI, G ;
YAMAMOTO, K ;
ITO, K ;
TSURUOKA, N ;
OKUDAIRA, H .
INTERNATIONAL IMMUNOLOGY, 1995, 7 (03) :449-457
[19]  
NAORA H, 1994, J IMMUNOL, V153, P3466
[20]  
NAORA H, 1994, BLOOD, V83, P3620