Negative regulation of cytokine gene transcription

被引:32
作者
Ye, JP [1 ]
Young, HA [1 ]
机构
[1] NCI, FREDERICK CANC RES & DEV CTR, DIV BASIC SCI, EXPT IMMUNOL LAB, FREDERICK, MD 21702 USA
关键词
nuclear factor; DNA methylation; T cell;
D O I
10.1096/fasebj.11.11.9285480
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
Cytokines are a class of soluble proteins that mediate signals throughout the immune system as well as between immune effector cells and other cell populations, This class of proteins includes interleukins, interferons, and chemokines, The expression of cytokines is tightly controlled in the producing cells, and one of the most important regulatory steps in this control is gene transcription, The transcription of most cytokine genes is silent until a producing cell is activated by extracellular stimuli, It is very common that transcription of these genes initiates immediately upon activation and shuts down quickly even in the continuous presence of the stimulating agent, Work performed over the past decade has revealed much about the molecular mechanism responsible for transcriptional regulation of these genes, Positive and negative transcription factors function in a concerted manner to regulate transcription of a specific cytokine at the promoter or intron region. We focus on recent progress in the field of transcriptional regulation of cytokine genes with an emphasis on the negative regulation of cytokine gene transcription.
引用
收藏
页码:825 / 833
页数:9
相关论文
共 99 条
[1]   E1A-ASSOCIATED P300 AND CREB-ASSOCIATED CBP BELONG TO A CONSERVED FAMILY OF COACTIVATORS [J].
ARANY, Z ;
SELLERS, WR ;
LIVINGSTON, DM ;
ECKNER, R .
CELL, 1994, 77 (06) :799-800
[2]   ACTIVATION OF CAMP AND MITOGEN RESPONSIVE GENES RELIES ON A COMMON NUCLEAR FACTOR [J].
ARIAS, J ;
ALBERTS, AS ;
BRINDLE, P ;
CLARET, FX ;
SMEAL, T ;
KARIN, M ;
FERAMISCO, J ;
MONTMINY, M .
NATURE, 1994, 370 (6486) :226-229
[3]  
ARYA SK, 1984, J IMMUNOL, V133, P273
[4]   The CBP co-activator is a histone acetyltransferase [J].
Bannister, AJ ;
Kouzarides, T .
NATURE, 1996, 384 (6610) :641-643
[5]   CBP-INDUCED STIMULATION OF C-FOS ACTIVITY IS ABROGATED BY E1A [J].
BANNISTER, AJ ;
KOUZARIDES, T .
EMBO JOURNAL, 1995, 14 (19) :4758-4762
[6]  
Bannister AJ, 1995, ONCOGENE, V11, P2509
[7]   Identification of a calcium-inducible, cyclosporine-sensitive element in the IFN-gamma promoter that is a potential NFAT binding site [J].
Campbell, PM ;
Pimm, J ;
Ramassar, V ;
Halloran, PF .
TRANSPLANTATION, 1996, 61 (06) :933-939
[8]  
Cantorna MT, 1996, J IMMUNOL, V156, P2674
[9]   INHIBITION OF NF-AT-DEPENDENT TRANSCRIPTION BY NF-KAPPA-B - IMPLICATIONS FOR DIFFERENTIAL GENE-EXPRESSION IN T-HELPER CELL SUBSETS [J].
CASOLARO, V ;
GEORAS, SN ;
SONG, ZM ;
ZUBKOFF, ID ;
ABDULKADIR, SA ;
THANOS, D ;
ONO, SJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (25) :11623-11627
[10]   Role of CBP/P300 in nuclear receptor signalling [J].
Chakravarti, D ;
LaMorte, VJ ;
Nelson, MC ;
Nakajima, T ;
Schulman, IG ;
Juguilon, H ;
Montminy, M ;
Evans, RM .
NATURE, 1996, 383 (6595) :99-103