REPRESSION OF I-A-BETA GENE-EXPRESSION BY THE TRANSCRIPTION FACTOR PU.1

被引:34
作者
BORRAS, FE
LLOBERAS, J
MAKI, RA
CELADA, A
机构
[1] UNIV BARCELONA, FAC BIOL, DEPT FISIOL IMMUNOL, E-08028 BARCELONA, SPAIN
[2] UNIV BARCELONA, FDN AUGUST PI & SUNYER, E-08028 BARCELONA, SPAIN
[3] LA JOLLA CANC RES FDN, LA JOLLA, CA 92037 USA
关键词
D O I
10.1074/jbc.270.41.24385
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
The PU.1 protein is an ets-related transcription factor that is expressed in macrophages and B lymphocytes. We present evidence that PU.1 binds to the promoter of the I-A beta gene, i.e. a PU box located next to the Y box. Transfection of PU.1 in B lymphocytes or in interferon-gamma-treated macrophages represses I-A beta gene expression. The inhibitory effect of PU.1 was obtained with the DNA binding domain of the protein, but not with the activation domain. Using the gel shift retardation assay we found that in vitro transcribed/translated NF-YA and NF-YB bind to the Y box of the I-A beta promoter. When PU.1 was added to the assay, a supershifted DNA band was found, indicating that PU.1 and NFY proteins bind to the same DNA molecule. We conclude that I-A beta gene expression is repressed by PU.1 binding to the PU box domain.
引用
收藏
页码:24385 / 24391
页数:7
相关论文
共 56 条
[1]   CHARACTERIZATION OF A CIS-ACTING REGULATORY ELEMENT WHICH SILENCES EXPRESSION OF THE CLASS II-A BETA-GENE IN EPITHELIUM [J].
ALBERT, SE ;
STRUTZ, F ;
SHELTON, K ;
HAVERTY, T ;
SUN, MJ ;
LI, SR ;
DENHAM, A ;
MAKI, RA ;
NEILSON, EG .
JOURNAL OF EXPERIMENTAL MEDICINE, 1994, 180 (01) :233-240
[2]   A SWITCH FROM MYC-MAX TO MAD-MAX HETEROCOMPLEXES ACCOMPANIES MONOCYTE/MACROPHAGE DIFFERENTIATION [J].
AYER, DE ;
EISENMAN, RN .
GENES & DEVELOPMENT, 1993, 7 (11) :2110-2119
[3]   REGULATION OF MAJOR HISTOCOMPATIBILITY COMPLEX CLASS-II GENES - X, Y AND OTHER LETTERS OF THE ALPHABET [J].
BENOIST, C ;
MATHIS, D .
ANNUAL REVIEW OF IMMUNOLOGY, 1990, 8 :681-715
[4]   THE EXPRESSION OF I-A CORRELATES WITH THE UPTAKE OF INTERFERON-GAMMA BY MACROPHAGES [J].
CELADA, A ;
MAKI, RA .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1989, 19 (01) :205-208
[5]   INTERFERON-GAMMA ACTIVATES MULTIPLE PATHWAYS TO REGULATE THE EXPRESSION OF THE GENES FOR MAJOR HISTOCOMPATIBILITY CLASS-II I-A-BETA, TUMOR NECROSIS FACTOR AND COMPLEMENT COMPONENT C-3 IN MOUSE MACROPHAGES [J].
CELADA, A ;
KLEMSZ, MJ ;
MAKI, RA .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1989, 19 (06) :1103-1109
[6]   REPRESSION OF MAJOR HISTOCOMPATIBILITY COMPLEX-IA EXPRESSION BY GLUCOCORTICOIDS - THE GLUCOCORTICOID RECEPTOR INHIBITS THE DNA-BINDING OF THE X-BOX DNA-BINDING PROTEIN [J].
CELADA, A ;
MCKERCHER, S ;
MAKI, RA .
JOURNAL OF EXPERIMENTAL MEDICINE, 1993, 177 (03) :691-698
[7]  
CELADA A, 1988, J IMMUNOL, V140, P3995
[8]   DNA-BINDING OF THE MOUSE CLASS-II MAJOR HISTOCOMPATIBILITY CCAAT FACTOR DEPENDS ON 2 COMPONENTS [J].
CELADA, A ;
MAKI, RA .
MOLECULAR AND CELLULAR BIOLOGY, 1989, 9 (07) :3097-3100
[9]  
CHEN HM, 1993, J BIOL CHEM, V268, P8230
[10]   MICE LACKING MHC CLASS-II MOLECULES [J].
COSGROVE, D ;
GRAY, D ;
DIERICH, A ;
KAUFMAN, J ;
LEMEUR, M ;
BENOIST, C ;
MATHIS, D .
CELL, 1991, 66 (05) :1051-1066