Hayashi Yuko, Kato Masaki, Seto Hirokazu, Yamaguchi Masamitsu
Division of Biochemistry, Aichi Cancer Center Research Institute, Nagoya 464-8681, Japan.
Biochim Biophys Acta. 2006 Jul;1759(7):359-66. doi: 10.1016/j.bbaexp.2006.07.002. Epub 2006 Jul 25.
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.
果蝇DNA复制相关元件结合因子(dDREF)对于许多携带DRE序列(5'-TATCGATA)的增殖相关基因的表达是必需的。在眼成虫盘过度表达dDREF会诱导异位DNA合成、细胞凋亡并抑制光感受器细胞特化,导致成虫出现粗糙眼表型。在本研究中,无翅基因(Dll)剂量减半增强了dDREF诱导的粗糙眼表型,表明Dll在眼成虫盘细胞中负向调节dDREF活性。生化分析显示,Dll的N端(第30个氨基酸至第124个氨基酸)和C端(第190个氨基酸至第327个氨基酸)区域与dDREF的DNA结合结构域(第16个氨基酸至第125个氨基酸)相互作用,不过尚不清楚这种相互作用是直接的还是间接的。电泳迁移率变动分析表明,Dll由此抑制DNA结合。像Dll这样的同源结构域蛋白对dDREF功能的抑制可能有助于在发育过程中对细胞增殖进行与分化相关的抑制。