Recognition of NFATp/AP-1 composite elements within genes induced upon the activation of immune cells

被引:98
作者
Kel, A
Kel-Margoulis, O
Babenko, V
Wingender, E
机构
[1] Russian Acad Sci, Inst Cytol & Genet, Novosibirsk 630090, Russia
[2] Gesell Biotechnol Forsch mbH, D-38124 Braunschweig, Germany
关键词
computer-assisted prediction; composite elements; NFATp/AP-1; immune response;
D O I
10.1006/jmbi.1999.2684
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
Composite elements are regulatory modules of promoters or enhancers that consist of binding sites of two different but synergizing transcription factors. A well-studied example is nuclear factors of activated T-cell (NFAT) sites which are composite elements of a NFATp/c and an activating protein 1 (AP-1) binding site. We have developed a computational approach to identify potential NFAT target genes which (a) comprises an improved method to scan for individual NFAT composite elements; (b) considers positional effects relative to transcription start sites; and (c) involves cluster analysis of potential NFAT composite elements. All three steps progressively helped to discriminate T-cell-specific promoter sequences against other functional regions (coding and intronic sequences) of the same genes, against promoters of muscle-specific genes or against random sequences. Using this approach, we identified potential NFAT composite elements in promoters of cytokine genes and their receptors as well as in promoters of genes for AP-1 family members, Ca2+-binding proteins and some other components of the regulatory network operating in activated T-cells and other immune cells. The method developed can be adapted to characterize and identify other composite elements as well. The program for recognition NFAT composite elements is available through the World Wide Web (http://compel.bionet.nsc.ru/FunSite/CompelScan.html and http://trans-fac.gbf.de/dbsearch/funsitep/s_comp.html). (C) 1999 Academic Press.
引用
收藏
页码:353 / 376
页数:24
相关论文
共 115 条
[1]   TRANSFORMING P21(RAS) MUTANTS AND C-ETS-2 ACTIVATE THE CYCLIN D1 PROMOTER THROUGH DISTINGUISHABLE REGIONS [J].
ALBANESE, C ;
JOHNSON, J ;
WATANABE, G ;
EKLUND, N ;
VU, D ;
ARNOLD, A ;
PESTELL, RG .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (40) :23589-23597
[2]   CYTOKINES - COORDINATORS OF IMMUNE AND INFLAMMATORY RESPONSES [J].
ARAI, K ;
LEE, F ;
MIYAJIMA, A ;
MIYATAKE, S ;
ARAI, N ;
YOKOTA, T .
ANNUAL REVIEW OF BIOCHEMISTRY, 1990, 59 :783-836
[3]   ACTIVATION AND EXPRESSION OF THE NUCLEAR FACTORS OF ACTIVATED T-CELLS, NFATP AND NFATC, IN HUMAN NATURAL-KILLER-CELLS - REGULATION UPON CD16 LIGAND-BINDING [J].
ARAMBURU, J ;
AZZONI, L ;
RAO, A ;
PERUSSIA, B .
JOURNAL OF EXPERIMENTAL MEDICINE, 1995, 182 (03) :801-810
[4]   SELECTION OF DNA-BINDING SITES BY REGULATORY PROTEINS .2. THE BINDING-SPECIFICITY OF CYCLIC-AMP RECEPTOR PROTEIN TO RECOGNITION SITES [J].
BERG, OG ;
VONHIPPEL, PH .
JOURNAL OF MOLECULAR BIOLOGY, 1988, 200 (04) :709-723
[5]   SELECTION OF DNA-BINDING SITES BY REGULATORY PROTEINS - STATISTICAL-MECHANICAL THEORY AND APPLICATION TO OPERATORS AND PROMOTERS [J].
BERG, OG ;
VONHIPPEL, PH .
JOURNAL OF MOLECULAR BIOLOGY, 1987, 193 (04) :723-743
[6]   THE NFAT-1 DNA-BINDING COMPLEX IN ACTIVATED T-CELLS CONTAINS FRA-1 AND JUNB [J].
BOISE, LH ;
PETRYNIAK, B ;
MAO, XH ;
JUNE, CH ;
WANG, CY ;
LINDSTEN, T ;
BRAVO, R ;
KOVARY, K ;
LEIDEN, JM ;
THOMPSSON, CB .
MOLECULAR AND CELLULAR BIOLOGY, 1993, 13 (03) :1911-1919
[7]   THE IMMUNOSUPPRESSIVES FK-506 AND CYCLOSPORINE-A INHIBIT THE GENERATION OF PROTEIN FACTORS BINDING TO THE 2 PURINE BOXES OF THE INTERLEUKIN-2 ENHANCER [J].
BRABLETZ, T ;
PIETROWSKI, I ;
SERFLING, E .
NUCLEIC ACIDS RESEARCH, 1991, 19 (01) :61-67
[8]  
BRAZMA A, 1997, P GERM C BIOINF GCB, P57
[9]   WEIGHT MATRIX DESCRIPTIONS OF 4 EUKARYOTIC RNA POLYMERASE-II PROMOTER ELEMENTS DERIVED FROM 502 UNRELATED PROMOTER SEQUENCES [J].
BUCHER, P .
JOURNAL OF MOLECULAR BIOLOGY, 1990, 212 (04) :563-578
[10]   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