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

被引:137
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