Cloning and characterization of the Drosophila homologue of the AP-2 transcription factor

被引:26
作者
Bauer, R
McGuffin, ME
Mattox, W
Tainsky, MA
机构
[1] Univ Texas, Md Anderson Canc Ctr, Dept Tumor Biol, Houston, TX 77030 USA
[2] Univ Texas, Md Anderson Canc Ctr, Dept Mol Genet, Houston, TX 77030 USA
关键词
Drosophila; AP-2 transcription factor; development regulation; functional conservation;
D O I
10.1038/sj.onc.1202114
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 AP-2 family of transcription factors (AP-2 alpha, AP-2 beta and AP-2 gamma) is temporally and spatially regulated in mammals and has also been implicated in oncogenesis. Here we report the isolation of genomic and cDNA clones encoding the Drosophila homologue of AP-2, designated DAP-2. The predicted amino acid sequence exhibits 42-45% overall identity with the vertebrate AP-2 proteins, A sequence of 107 amino acids within the DNA binding and dimerization domain of the vertebrate AP-2 proteins is highly conserved (90-92%) with the DAP-2 homologue. An in vitro translation product of DAP-2 cDNA binds specifically to AP-2 consensus binding sites. DAP-2 was also shown to be functionally conserved in vivo because transient transfection of a DAP-2 expression plasmid activated transcription through AP-2 binding sites in both mammalian and Drosophila cell lines. DAP-2 is expressed during early embryogenesis and DAP-2 transcripts are also detected in the adult. Whole-mount in situ hybridizations demonstrated that DAP-2 is expressed initially at stage 9 of Drosophila embryonic development and that DAP-2 transcripts are detected in regions of the brain, eye-antennal disc, optical lobe, antenno-maxillary complex, and in a subset of cells of the ventral nerve cord. The cloning of DAP-2 and the identification of the DAP-2 expression pattern during embryogenesis provides a starting point to address the function of AP-2 during differentiation and development in a well understood model system.
引用
收藏
页码:1911 / 1922
页数:12
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