STRUCTURE AND REGULATION OF THE CHICKEN GATA-3 GENE

被引:8
作者
ISHIHARA, H
ENGEL, JD
YAMAMOTO, M
机构
[1] TOHOKU UNIV,SCH MED,DEPT BIOCHEM,AOBA KU,SENDAI,MIYAGI 98077,JAPAN
[2] NORTHWESTERN UNIV,DEPT BIOCHEM MOLEC BIOL & CELL BIOL,EVANSTON,IL 60208
关键词
GATA-3; T CELL; TRANSCRIPTION FACTOR; TRANSCRIPTIONAL REGULATION;
D O I
10.1093/oxfordjournals.jbchem.a124736
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
To elucidate the mechanisms underlying the tissue-restricted expression of GATA factor transcription, we have isolated and analyzed the genomic chicken GATA-3 (cGATA-3) locus. Structural analysis of the clones showed that the cGATA-3 gene consists of six exons which span more than 19 kb. Two trans-activating domains and two Zn finger domains of cGATA-3 were found to be encoded separately by exons 2/3 and 4/5, respectively, indicating that each functional domain of GATA-3 is encoded by a discrete exon. We have determined 1.7 kb of upstream promoter sequence and found a number of sequence motifs which match those of known transcription factor binding sites. Activities of presumptive regulatory regions of this gene were assessed by transfecting chimeric constructs into a chicken T cell line MSB-1. The results showed three features of cGATA-3 gene regulation. The basal promoter activity of the cGATA-3 gene is determined by sequences lying between -104 and -29 bp of the promoter region. The upstream region containing the GATA and CACCC elements in close proximity (-1280 to -1152) appeared to act as a negative transcriptional regulator, whereas the region -1151 to -850 acts as a positive regulator. Thus, the expression of cGATA-3 gene is under complex regulation and the mode of regulation of cGATA-3 gene expression is suggested to be different from that of GATA-1 genes.
引用
收藏
页码:499 / 508
页数:10
相关论文
共 53 条
[1]  
ABEL T, 1993, DEVELOPMENT, V119, P623
[2]  
AKIYAMA Y, 1974, BIKEN J, V17, P105
[3]   MOUSE GATA-4 - A RETINOIC ACID-INDUCIBLE GATA-BINDING TRANSCRIPTION FACTOR EXPRESSED IN ENDODERMALLY DERIVED TISSUES AND HEART [J].
ARCECI, RJ ;
KING, AAJ ;
SIMON, MC ;
ORKIN, SH ;
WILSON, DB .
MOLECULAR AND CELLULAR BIOLOGY, 1993, 13 (04) :2235-2246
[4]   SCREENING GAMMAGT RECOMBINANT CLONES BY HYBRIDIZATION TO SINGLE PLAQUES INSITU [J].
BENTON, WD ;
DAVIS, RW .
SCIENCE, 1977, 196 (4286) :180-182
[5]   TRANSCRIPTION TERMINATION AND 3' PROCESSING - THE END IS IN SITE [J].
BIRNSTIEL, ML ;
BUSSLINGER, M ;
STRUB, K .
CELL, 1985, 41 (02) :349-359
[6]  
CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2
[7]   EXPRESSION OF THE DAL80 GENE, WHOSE PRODUCT IS HOMOLOGOUS TO THE GATA FACTORS AND IS A NEGATIVE REGULATOR OF MULTIPLE NITROGEN CATABOLIC GENES IN SACCHAROMYCES-CEREVISIAE, IS SENSITIVE TO NITROGEN CATABOLITE REPRESSION [J].
CUNNINGHAM, TS ;
COOPER, TG .
MOLECULAR AND CELLULAR BIOLOGY, 1991, 11 (12) :6205-6215
[8]  
DORFMAN DM, 1992, J BIOL CHEM, V267, P1279
[9]   OLIGODEOXYRIBONUCLEOTIDE LIGATION TO SINGLE-STRANDED CDNAS - A NEW TOOL FOR CLONING 5'-ENDS OF MESSENGER-RNAS AND FOR CONSTRUCTING CDNA LIBRARIES BY INVITRO AMPLIFICATION [J].
EDWARDS, JBDM ;
DELORT, J ;
MALLET, J .
NUCLEIC ACIDS RESEARCH, 1991, 19 (19) :5227-5232
[10]  
ENGEL JD, 1991, SEMIN HEMATOL, V28, P158