Comparison of human and Xenopus GATA-2 promoters

被引:15
作者
Fleenor, DE
Langdon, SD
deCastro, CM
Kaufman, RE
机构
[1] Duke University Medical Center, Box 3250, Department of Medicine, Durham
关键词
ets factors; CCAAT factors; gene; cloning; erythropoiesis;
D O I
10.1016/S0378-1119(96)00355-1
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
GATA proteins comprise a family of transcription factors that are required for appropriate development of hematopoietic lineages. In order to understand the transcriptional regulation of GATA genes, we have cloned the human GATA-2 gene and identified and characterized its promoter. Comparison with the Xenopus GATA-2 promoter demonstrates highly conserved CCAAT box elements, which are essential for appropriate Xenopus expression. Unlike the Xenopus gene, the human GATA-2 gene lacks GATA binding motifs within the first 800 bp of 5' flanking sequence. In addition, the human GATA-2 promoter has two highly conserved ets sites that resemble the binding site for a recently described ets repressor factor, ERF. These conserved DNA sequence motifs provide strong candidate regions for the regulation of GATA-2.
引用
收藏
页码:219 / 223
页数:5
相关论文
共 48 条
[21]  
LEE ME, 1991, J BIOL CHEM, V266, P16188
[22]  
LEONARD M, 1993, BLOOD, V82, P1071
[23]   THE ETS GENE FAMILY [J].
MACLEOD, K ;
LEPRINCE, D ;
STEHELIN, D .
TRENDS IN BIOCHEMICAL SCIENCES, 1992, 17 (07) :251-256
[24]   THE HUMAN ENHANCER-BINDING PROTEIN GATA3 BINDS TO SEVERAL T-CELL RECEPTOR REGULATORY ELEMENTS [J].
MARINE, J ;
WINOTO, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (16) :7284-7288
[25]   TRANSCRIPTIONAL ACTIVATION AND DNA-BINDING BY THE ERYTHROID FACTOR GF-1/NF-E1/ERYF-1 [J].
MARTIN, DIK ;
ORKIN, SH .
GENES & DEVELOPMENT, 1990, 4 (11) :1886-1898
[26]  
MAVROTHALASSITIS GJ, 1991, CELL GROWTH DIFFER, V2, P215
[27]  
MINIE M, 1992, J CELL SCI S, V16, P15
[28]  
MOUTHON MA, 1993, BLOOD, V81, P647
[29]   TRANSCRIPTION FACTOR GATA-2 IS EXPRESSED IN ERYTHROID, EARLY MYELOID, AND CD34+ HUMAN LEUKEMIA-DERIVED CELL-LINES [J].
NAGAI, T ;
HARIGAE, H ;
ISHIHARA, H ;
MOTOHASHI, H ;
MINEGISHI, N ;
TSUCHIYA, S ;
HAYASHI, N ;
GU, L ;
ANDRES, B ;
ENGEL, JD ;
YAMAMOTO, M .
BLOOD, 1994, 84 (04) :1074-1084
[30]  
ORKIN SH, 1992, BLOOD, V80, P575