THE ZEBRAFISH EGR1 GENE ENCODES A HIGHLY CONSERVED, ZINC-FINGER TRANSCRIPTIONAL REGULATOR

被引:16
作者
DRUMMOND, IA
ROHWERNUTTER, P
SUKHATME, VP
机构
[1] BETH ISRAEL HOSP, DEPT MED, DIV RENAL, BOSTON, MA 02215 USA
[2] UNIV WISCONSIN, MCARDLE LAB CANC RES, MADISON, WI 53706 USA
关键词
D O I
10.1089/dna.1994.13.1047
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 Egr family of transcriptional regulators comprises a group of genes which encode members of the Cys(2)-His(2) class of zinc-finger proteins. We have isolated a zebrafish egr1 homologue by screening a zebrafish genomic library with a mouse Egr1 zinc finger probe. Southern blotting indicated the existence of a single zebrafish egr1 gene and, as in higher vertebrates, the presence of related members of a larger gene family. Sequence analysis of the zebrafish egr1 coding region revealed a high level of homology to the mouse, rat, and human Egr1 genes with the notable exception of a polymorphic, triplet nucleotide repeat sequence in the region coding for the amino terminus of the Egr1 protein. The predicted DNA-binding, zinc-finger domain protein sequence was strictly conserved. The 5' region of the zebrafish egr1 gene contained a variety of transcription factor binding sites, also present in the mouse gene, for serum response factor, CREB and c-Ets. The zebrafish egr1 transcript was approximately 3.4 kb in size and was expressed in adult zebrafish brain and muscle RNA, a pattern of expression similar to that observed in mice. The potential for zebrafish egr1 to function as a transcriptional regulator was tested by constructing an expression vector containing zebrafish egr1 coding sequences under the control of a cytomegalovirus promoter. This construct was found to activate transcription of a reporter plasmid bearing multiple Egr1 binding sites when transiently cotransfected into mouse 3T3 cells. Our results indicate that the structure, regulation, and function of the Egr1 gene have been highly conserved during vertebrate evolution and suggest an important role for this gene in growth and development.
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页码:1047 / 1055
页数:9
相关论文
共 39 条
[1]  
ANDERSSON S, 1989, J BIOL CHEM, V264, P8222
[2]  
BAYER TA, 1992, DEVELOPMENT, V115, P421
[3]   The CREB family of transcription activators [J].
Brindle, Paul K. ;
Montminy, Marc R. .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 1992, 2 (02) :199-204
[4]   TRIPLET REPEAT MUTATIONS IN HUMAN-DISEASE [J].
CASKEY, CT ;
PIZZUTI, A ;
FU, YH ;
FENWICK, RG ;
NELSON, DL .
SCIENCE, 1992, 256 (5058) :784-789
[5]  
CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2
[6]   FUNCTIONAL SERUM RESPONSE ELEMENTS UPSTREAM OF THE GROWTH FACTOR-INDUCIBLE GENE ZIF268 [J].
CHRISTY, B ;
NATHANS, D .
MOLECULAR AND CELLULAR BIOLOGY, 1989, 9 (11) :4889-4895
[7]   DNA-BINDING SITE OF THE GROWTH FACTOR-INDUCIBLE PROTEIN ZIF268 [J].
CHRISTY, B ;
NATHANS, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (22) :8737-8741
[8]   A GENE ACTIVATED IN MOUSE 3T3-CELLS BY SERUM GROWTH-FACTORS ENCODES A PROTEIN WITH ZINC FINGER SEQUENCES [J].
CHRISTY, BA ;
LAU, LF ;
NATHANS, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (21) :7857-7861
[9]   HIGH-FREQUENCY GERM-LINE TRANSMISSION OF PLASMID DNA-SEQUENCES INJECTED INTO FERTILIZED ZEBRAFISH EGGS [J].
CULP, P ;
NUSSLEINVOLHARD, C ;
HOPKINS, N .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (18) :7953-7957
[10]   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