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果蝇skpA基因被鉴定为转录因子DREF的一个新靶点。

Identification of the Drosophila skpA gene as a novel target of the transcription factor DREF.

作者信息

Phuong Thao Dang Thi, Ida Hiroyuki, Yoshida Hideki, Yamaguchi Masamitsu

机构信息

Department of Applied Biology, Kyoto Institute of Technology, Matsugasaki, Sakyo-ku, Kyoto 606-8585, Japan.

出版信息

Exp Cell Res. 2006 Nov 1;312(18):3641-50. doi: 10.1016/j.yexcr.2006.08.005. Epub 2006 Aug 14.

Abstract

SKPa is component of a Drosophila SCF complex that functions in combination with the ubiquitin-conjugating enzyme UbcD1. skpA null mutation results in centrosome overduplication, unusual chromatin condensation, defective endoreduplication and cell-cycle progression. While the molecular mechanisms that regulate expression of the skpA gene are poorly understood, the DNA replication-related element (DRE) and the DRE-binding factor (DREF) play important roles in regulating proliferation-related genes in Drosophila and DRE (5'-TATCGATA) and DRE-like (5'-CATCGATT) sequences were here found to be involved in skpA promoter activity. Thus both luciferase transient expression assays in cultured Drosophila S2 cells using skpA promoter-luciferase fusion plasmids and anti-lacZ immunostaining of various tissues from transgenic third instar larvae carrying the skpA promoter-lacZ fusion genes provided supportive evidence. Furthermore, anti-SKPa immunostaining of eye imaginal discs from flies overexpressing DREF showed ectopic expression of protein in the region posterior to the morphogenetic furrow where DREF is overexpressed. Knockdown of DREF in some tissues where SKPa distribution is well known almost completely abrogated the skpA gene expression. These findings, taken together, indicate that the Drosophila skpA gene is a novel target of the transcription factor DREF.

摘要

SKPa是果蝇SCF复合物的一个组成部分,它与泛素结合酶UbcD1协同发挥作用。skpA基因的无效突变会导致中心体过度复制、异常的染色质浓缩、有缺陷的核内复制和细胞周期进程。虽然调节skpA基因表达的分子机制尚不清楚,但DNA复制相关元件(DRE)和DRE结合因子(DREF)在调节果蝇增殖相关基因方面发挥着重要作用,并且在这里发现DRE(5'-TATCGATA)和类DRE(5'-CATCGATT)序列参与了skpA启动子活性。因此,使用skpA启动子-荧光素酶融合质粒在培养的果蝇S2细胞中进行的荧光素酶瞬时表达分析以及对携带skpA启动子-lacZ融合基因的转基因三龄幼虫的各种组织进行的抗lacZ免疫染色都提供了支持性证据。此外,对过表达DREF的果蝇眼成虫盘进行抗SKPa免疫染色,结果显示在形态发生沟后方DREF过表达的区域有异位蛋白表达。在一些已知SKPa分布的组织中敲低DREF几乎完全消除了skpA基因的表达。综合这些发现表明,果蝇skpA基因是转录因子DREF的一个新靶点。

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