IDENTIFICATION OF PROTEIN-BINDING DNA-SEQUENCES IN AN AUXIN-REGULATED GENE OF SOYBEAN

被引:63
作者
NAGAO, RT
GOEKJIAN, VH
HONG, JC
KEY, JL
机构
[1] Department of Botany, University of Georgia, Athens, 30602, GA
关键词
AUXIN-REGULATED GENE; DNASE-I FOOTPRINTING; GEL MOBILITY SHIFT ASSAY; PROTEIN BINDING DNA SEQUENCE; SOYBEAN;
D O I
10.1007/BF00023610
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
The promoter region of a soybean auxin-responsive gene, GmAux28, was analyzed to identify protein-binding DNA sequences that may be involved in regulation of expression. Using DNase I footprinting and gel mobility shift assays, multiple regions of interaction, including eight major protein-binding sites, were observed in the GmAux28 gene. Two sequence motifs, TGACGACA and TCCACGTGTC, related to as-l/Hex and G-box elements, respectively, found in several plant promoters, were identified. Four distinct A/T-rich domains were identified; such A/T-rich domains appear to modulate, but not to specify, the expression of many genes. Two new sequence motifs, delta-1 (DI) and delta-4 (D4) were also identified. D1 and D4 share a very similar core sequence, TAGTxxCTGT and TAGTxCTGT, respectively. In gel mobility shift analyses, D1 and D4 elements exhibit a complex interaction of binding proteins. The GmAux22 promoter also contains D1-related elements which compete with the GmAux28 elements. Sequence comparisons have identified D1/D4-like sequences in several other auxin-responsive genes suggesting the possible importance of D1/D4 and the respective binding proteins in the regulation of expression of these genes.
引用
收藏
页码:1147 / 1162
页数:16
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