DRIFTER, A DROSOPHILA POU-DOMAIN TRANSCRIPTION FACTOR, IS REQUIRED FOR CORRECT DIFFERENTIATION AND MIGRATION OF TRACHEAL CELLS AND MIDLINE GLIA

被引:135
作者
ANDERSON, MG [1 ]
PERKINS, GL [1 ]
CHITTICK, P [1 ]
SHRIGLEY, RJ [1 ]
JOHNSON, WA [1 ]
机构
[1] UNIV IOWA, COLL MED, DEPT PHYSIOL & BIOPHYS, GENET PHD PROGRAM, IOWA CITY, IA 52242 USA
关键词
DROSOPHILA; NEURON; GLIA; POU DOMAIN; CELL MIGRATION; TRACHEA;
D O I
10.1101/gad.9.1.123
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The Drosophila drifter (dfr) gene, previously referred to as Cf1a, encodes a POU-domain DNA-binding protein implicated as a neuron-specific regulator in the developing central nervous system (CNS). We have isolated full-length dfr cDNA clones that encode a 46-kD protein containing the conserved POU-domain DNA-binding domain. The use of alternate polyadenylation sites produces two dfr mRNA transcripts that are first expressed in stage 10 embryos at 5- to 6-hr of development. A specific anti-dfr polyclonal antiserum generated against a dfr-glutathione S-transferase fusion protein recognizes a 46-kD protein on Western blots and has been used to analyze the cell-specific distribution of dfr protein during embryonic development. dfr protein is distributed in a complex expression pattern including the tracheal system, the middle pair of midline glia, and selected CNS neurons. We have carried out a genetic characterization of the dfr locus, previously localized to region 65D of the third chromosome, by generating a series of overlapping deficiencies between 65A and 65E1 that were used to isolate dfr(E82), an EMS-induced lethal allele. Analysis of dfr(E82) mutant embryos shows a disruption of the developing tracheal tree as well as commissural defects in the developing CNS. Based on an examination of a cell-specific marker for tracheal cells and midline glia, these defects appear to be caused by a failure of these cells to follow their characteristic routes of migration. The dfr(E82) tracheal phenotype is rescued by a dfr minigene present as a P-element transposon expressing wild-type dfr protein in tracheal cells. These results suggest that the dfr protein plays a fundamental role in the differentiation of tracheal cells and midline glia possibly by regulating the expression of essential cell-surface proteins required for cell-cell interactions involved in directed cell migrations.
引用
收藏
页码:123 / 137
页数:15
相关论文
共 79 条
[1]   XLPOU 1 AND XLPOU 2, 2 NOVEL POU DOMAIN GENES EXPRESSED IN THE DORSOANTERIOR REGION OF XENOPUS EMBRYOS [J].
AGARWAL, VR ;
SATO, SM .
DEVELOPMENTAL BIOLOGY, 1991, 147 (02) :363-373
[2]  
ANDERSEN B, 1993, J BIOL CHEM, V268, P23390
[3]  
ASHBURNER M, 1989, DROSOPHILA LABORATOR
[4]   THE SOLUTION STRUCTURE OF THE OCT-1 POU-SPECIFIC DOMAIN REVEALS A STRIKING SIMILARITY TO THE BACTERIOPHAGE-LAMBDA REPRESSOR DNA-BINDING DOMAIN [J].
ASSAMUNT, N ;
MORTISHIRESMITH, RJ ;
AURORA, R ;
HERR, W ;
WRIGHT, PE .
CELL, 1993, 73 (01) :193-205
[5]   NUCLEOTIDE-SEQUENCE OF XLPOU3 CDNA, A MEMBER OF THE POU DOMAIN GENE FAMILY EXPRESSED IN XENOPUS-LAEVIS EMBRYOS [J].
BALTZINGER, M ;
PAYEN, E ;
REMY, P .
NUCLEIC ACIDS RESEARCH, 1992, 20 (08) :1993-1993
[6]  
BHAT KM, 1994, DEVELOPMENT, V120, P1483
[7]   ISOLATION OF A FAMILY OF DROSOPHILA POU DOMAIN GENES EXPRESSED IN EARLY DEVELOPMENT [J].
BILLIN, AN ;
COCKERILL, KA ;
POOLE, SJ .
MECHANISMS OF DEVELOPMENT, 1991, 34 (2-3) :75-84
[8]   MOBILIZATION OF HOBO ELEMENTS RESIDING WITHIN THE DECAPENTAPLEGIC GENE-COMPLEX - SUGGESTION OF A NEW HYBRID DYSGENESIS SYSTEM IN DROSOPHILA-MELANOGASTER [J].
BLACKMAN, RK ;
GRIMAILA, R ;
KOEHLER, MMD ;
GELBART, WM .
CELL, 1987, 49 (04) :497-505
[9]   ENVIRONMENTAL-INFLUENCES ON NEURAL CREST CELL-MIGRATION [J].
BRONNERFRASER, M .
JOURNAL OF NEUROBIOLOGY, 1993, 24 (02) :233-247
[10]   FUNCTIONAL CDNA LIBRARIES FROM DROSOPHILA EMBRYOS [J].
BROWN, NH ;
KAFATOS, FC .
JOURNAL OF MOLECULAR BIOLOGY, 1988, 203 (02) :425-437