Drosophila distal-less negatively regulates dDREF by inhibiting its DNA binding activity

被引:16
作者
Hayashi, Yuko
Kato, Masaki
Seto, Hirokazu
Yamaguchi, Masamitsu [1 ]
机构
[1] Kyoto Inst Technol, Dept Appl Biol, Sakyo Ku, Kyoto 6068585, Japan
[2] Aichi Canc Ctr, Res Inst, Div Biochem, Nagoya, Aichi 464, Japan
[3] Kyoto Inst Technol, Venture Lab, Sakyo Ku, Kyoto 6068585, Japan
[4] Kyoto Inst Technol, Insect Biomed Res Ctr, Sakyo Ku, Kyoto 6068585, Japan
来源
BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION | 2006年 / 1759卷 / 07期
关键词
DNA replication-related element binding factor (DREF); distal-less; DNA binding; proliferation; transcription factor;
D O I
10.1016/j.bbaexp.2006.07.002
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 Drosophila DNA replication-related element binding factor (dDREF) is required for expression of many proliferation-related genes carrying the DRE sequence, 5'-TATCGATA. Over-expression of dDREF in the eye imaginal disc induces ectopic DNA synthesis, apoptosis and inhibition of photoreceptor cell specification, and results in rough eye phenotype in adults. In the present study, half dose reduction of the Distal-less (Dll) gene enhanced the dDREF-induced rough eye phenotype, suggesting that Dll negatively regulates dDREF activity in eye imaginal disc cells. Biochemical analyses revealed the N-terminal (30aa to 124aa) and C-terminal (190aa to 327aa) regions of Dll to interact with the DNA binding domain (16aa to 125aa) of dDREF, although it is not clear yet whether the interaction is direct or indirect. Electrophoretic mobility shift assays showed that Dll thereby inhibits DNA binding. The repression of this dDREF-function by a homeodomain protein like Dll may contribute to the differentiation-coupled repression of cell proliferation during development. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:359 / 366
页数:8
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