Identification of three conserved regions in the DREF transcription factors from Drosophila melanogaster and Drosophila virilis

Citation
Y. Takahashi et al., Identification of three conserved regions in the DREF transcription factors from Drosophila melanogaster and Drosophila virilis, NUCL ACID R, 27(2), 1999, pp. 510-516
Citations number
32
Categorie Soggetti
Biochemistry & Biophysics
Journal title
NUCLEIC ACIDS RESEARCH
ISSN journal
03051048 → ACNP
Volume
27
Issue
2
Year of publication
1999
Pages
510 - 516
Database
ISI
SICI code
0305-1048(19990115)27:2<510:IOTCRI>2.0.ZU;2-9
Abstract
The genes for a DNA replication-related element-binding factor (DREF) were isolated from Drosophila melanogaster and Drosophila virilis,and their nucl eotide sequences were determined. Drosophila virilis DREF consists of 742 a mino acid residues, which is 33 amino acids longer than D. melanogaster DRE F. Comparison of the amino acid sequences revealed that D,virilis DREF is 7 1% identical to its D. melanogaster homolog, Three highly conserved regions were identified at amino acid positions 14-182 (CR1), 432-568 (CR2) and 63 6-730 (CR3) of the D. virilis DREF, with 86.4, 86.1 and 83.3% identities, r espectively. Transgenic flies in which expression of three conserved region s of D. melanogaster DREF was targeted to the eye imaginal disc were establ ished. Expression of CR1 in the developing eye imaginal discs resulted in a severe rough eye phenotype in adult flies. Expression of CR3 also caused a rough eye phenotype, while that of CR2 had no apparent effect on eye morph ology, Expression of either CR1 or CR3 in eye imaginal disc cells inhibited cell cycle progression and reduced incorporation of 5-bromo-2'-deoxyuridin e into the S-phase zone (the second mitotic wave) behind the morphogenetic furrow. The results indicate that both CR1 and CR3 are important for DREF f unctions.