DNA-BINDING FACTOR GT-2 FROM ARABIDOPSIS

被引:70
作者
KUHN, RM
CASPAR, T
DEHESH, K
QUAIL, PH
机构
[1] UNIV CALIF BERKELEY,DEPT PLANT BIOL,BERKELEY,CA 94720
[2] USDA,CTR PLANT GENE EXPRESS,ALBANY,CA 94710
关键词
ARABIDOPSIS; DNA-BINDING FACTOR; GT-2; PLANT GENE REGULATION; TRANSCRIPTION FACTOR; TRIHELIX;
D O I
10.1007/BF00029009
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
Complementary DNA clones encoding a DNA-binding factor have been obtained from Arabidopsis by DNA hybridization with a GT-2 factor cDNA clone from rice. The GT-2 gene appears to be present as a single copy in the Arabidopsis genome and is transcribed as a 2.1 kb mRNA which is not light-regulated. The longest open reading frame in the sequenced clones predicts a protein of 65 kDa, beginning with the first in-frame methionine. The protein contains basic, acidic, and proline/glutamine-rich motifs and has significant amino acid sequence homology to the rice GT-2 factor, including three regions of 50-75 amino acids each of greater than 60% identity. Two of these regions are predicted to form similar trihelix structures postulated to be involved in selective binding to specific variations of a GT-box motif DNA sequence found in the promoter regions of several plant genes. Except for weak similarity to a tobacco GT-box binding factor, GT-1a/B2F, Arabidopsis GT-2 has no similarity to other sequences in the databases. DNA-binding studies show that Arabidopsis GT-2 has binding characteristics similar to those of the rice GT-2 factor, but dissimilar to those of the tobacco GT- 1 a/B2F factor. The data indicate that a DNA-binding factor containing domains of similar structure and target-sequence specificity has been conserved between monocots and dicots.
引用
收藏
页码:337 / 348
页数:12
相关论文
共 40 条
[1]   THE GENE FAMILY ENCODING THE ARABIDOPSIS-THALIANA TRANSLATION ELONGATION-FACTOR EF-1-ALPHA - MOLECULAR-CLONING, CHARACTERIZATION AND EXPRESSION [J].
AXELOS, M ;
BARDET, C ;
LIBOZ, T ;
LEVANTHAI, A ;
CURIE, C ;
LESCURE, B .
MOLECULAR & GENERAL GENETICS, 1989, 219 (1-2) :106-112
[2]   A NEGATIVELY ACTING DNA-SEQUENCE ELEMENT MEDIATES PHYTOCHROME-DIRECTED REPRESSION OF PHYA GENE-TRANSCRIPTION [J].
BRUCE, WB ;
DENG, XW ;
QUAIL, PH .
EMBO JOURNAL, 1991, 10 (10) :3015-3024
[3]  
CASPAR T, 1993, PLANT J, V3, P161, DOI 10.1111/j.1365-313X.1993.tb00019.x
[4]   EMPIRICAL PREDICTIONS OF PROTEIN CONFORMATION [J].
CHOU, PY ;
FASMAN, GD .
ANNUAL REVIEW OF BIOCHEMISTRY, 1978, 47 :251-276
[5]   SEQUENCE AND NITRATE REGULATION OF THE ARABIDOPSIS-THALIANA MESSENGER-RNA ENCODING NITRATE REDUCTASE, A METALLOFLAVOPROTEIN WITH 3 FUNCTIONAL DOMAINS [J].
CRAWFORD, NM ;
SMITH, M ;
BELLISSIMO, D ;
DAVIS, RW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (14) :5006-5010
[6]   A TRANS-ACTING FACTOR THAT BINDS TO A GT-MOTIF IN A PHYTOCHROME GENE PROMOTER [J].
DEHESH, K ;
BRUCE, WB ;
QUAIL, PH .
SCIENCE, 1990, 250 (4986) :1397-1399
[7]   GT-2 - A TRANSCRIPTION FACTOR WITH TWIN AUTONOMOUS DNA-BINDING DOMAINS OF CLOSELY RELATED BUT DIFFERENT TARGET SEQUENCE SPECIFICITY [J].
DEHESH, K ;
HUNG, H ;
TEPPERMAN, JM ;
QUAIL, PH .
EMBO JOURNAL, 1992, 11 (11) :4131-4144
[8]   A COMPREHENSIVE SET OF SEQUENCE-ANALYSIS PROGRAMS FOR THE VAX [J].
DEVEREUX, J ;
HAEBERLI, P ;
SMITHIES, O .
NUCLEIC ACIDS RESEARCH, 1984, 12 (01) :387-395
[9]   A TECHNIQUE FOR RADIOLABELING DNA RESTRICTION ENDONUCLEASE FRAGMENTS TO HIGH SPECIFIC ACTIVITY [J].
FEINBERG, AP ;
VOGELSTEIN, B .
ANALYTICAL BIOCHEMISTRY, 1983, 132 (01) :6-13
[10]   TURBO-SCREENING OF BACTERIAL COLONIES USING MICROWAVE DENATURATION ON PAPER FILTERS [J].
FORSTER, A ;
BULUWELA, L ;
RABBITTS, TH .
TRENDS IN GENETICS, 1990, 6 (05) :141-141