Mechanisms of transcriptional regulation of the human IL-3/GM-CSF locus by inducible tissue-specific promoters and enhancers

被引:21
作者
Cockerill, PN [1 ]
机构
[1] Univ Leeds, St Jamess Univ Hosp, Mol Med Unit, Leeds LS9 7TF, W Yorkshire, England
关键词
NFAT; enhancer; DNaseI hypersensitive sites; T cells; chromatin;
D O I
10.1615/CritRevImmunol.v24.i6.10
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The IL-3 and GM-CSF genes are closely linked in the genome and reside within a cluster of cytokine genes. IL-3 and GM-CSF are expressed in a highly inducible and tissue-specific pattern, and this review attempts to provide a comprehensive description of the key regulatory elements in this locus that control their expression. Although these genes are typically coexpressed in T cells, they are differentially regulated in many other cell types, whereby cells such as monocytes and endothelial cells express GM-CSF, but not IL-3. This suggests that they are likely to be regulated by distinct mechanisms. This view is reinforced by the identification of three inducible enhancers in the locus that have different specificities. These enhancers are embedded within arrays of tissue-specific DNaseI hypersensitive sites that most likely play additional roles in establishing distinct patterns of gene expression. This locus also represents a valuable model system for studying the role of chromatin remodeling in cytokine gene activation. NFAT is one inducible factor that appears to play a major role in the formation of DNaseI hypersensitive sites within enhancers, and which functions in a highly cooperative manner with other classes of transcription factors to direct specific patterns of cytokine gene expression.
引用
收藏
页码:385 / 408
页数:24
相关论文
共 73 条
[1]  
Alexander W S, 1998, Int Rev Immunol, V16, P651, DOI 10.3109/08830189809043013
[2]  
Annicotte JS, 2001, BIOTECHNIQUES, V31, P993
[3]   Affinity-driven peptide selection of an NFAT inhibitor more selective than cyclosporin A [J].
Aramburu, J ;
Yaffe, MB ;
López-Rodríguez, C ;
Cantley, LC ;
Hogan, PG ;
Rao, A .
SCIENCE, 1999, 285 (5436) :2129-2133
[4]   Generation of an improved luciferase reporter gene plasmid that employs a novel mechanism for high-copy replication [J].
Bert, AG ;
Burrows, J ;
Osborne, CS ;
Cockerill, PN .
PLASMID, 2000, 44 (02) :173-182
[5]   Reconstitution of T cell-specific transcription directed by composite NFAT/Oct elements [J].
Bert, AG ;
Burrows, J ;
Hawwari, A ;
Vadas, MA ;
Cockerill, PN .
JOURNAL OF IMMUNOLOGY, 2000, 165 (10) :5646-5655
[6]   A NF-κB/Sp1 region is essential for chromatin remodeling and correct transcription of a human granulocyte-macrophage colony-stimulating factor transgene [J].
Cakouros, D ;
Cockerill, PN ;
Bert, AG ;
Mital, R ;
Roberts, DC ;
Shannon, MF .
JOURNAL OF IMMUNOLOGY, 2001, 167 (01) :302-310
[7]   IDENTIFICATION OF A CRITICAL REGULATORY SITE IN THE HUMAN INTERLEUKIN-3 PROMOTER BY IN-VIVO FOOTPRINTING [J].
CAMERON, S ;
TAYLOR, DS ;
TEPAS, EC ;
SPECK, NA ;
MATHEYPREVOT, B .
BLOOD, 1994, 83 (10) :2851-2859
[8]   REGULATION OF EXPRESSION OF HUMAN GRANULOCYTE-MACROPHAGE COLONY-STIMULATING FACTOR [J].
CHAN, JY ;
SLAMON, DJ ;
NIMER, SD ;
GOLDE, DW ;
GASSON, JC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (22) :8669-8673
[9]  
COCKERILL GW, 1995, BLOOD, V86, P2689
[10]  
Cockerill P N, 2000, Methods Mol Biol, V130, P29