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果蝇Mi-2通过抑制dDREF的DNA结合活性来负向调节dDREF。

Drosophila Mi-2 negatively regulates dDREF by inhibiting its DNA-binding activity.

作者信息

Hirose Fumiko, Ohshima Nobuko, Kwon Eun-Jeong, Yoshida Hideki, Yamaguchi Masamitsu

机构信息

Division of Biochemistry, Aichi Cancer Center Research Institute, Chikusa-ku, Nagoya 464-8681, Japan.

出版信息

Mol Cell Biol. 2002 Jul;22(14):5182-93. doi: 10.1128/MCB.22.14.5182-5193.2002.

Abstract

Drosophila melanogaster DNA replication-related element (DRE) factor (dDREF) is a transcriptional regulatory factor required for the expression of genes carrying the 5'-TATCGATA DRE. dDREF has been reported to bind to a sequence in the chromatin boundary element, and thus, dDREF may play a part in regulating insulator activity. To generate further insights into dDREF function, we carried out a Saccharomyces cerevisiae two-hybrid screening with DREF polypeptide as bait and identified Mi-2 as a DREF-interacting protein. Biochemical analyses revealed that the C-terminal region of Drosophila Mi-2 (dMi-2) specifically binds to the DNA-binding domain of dDREF. Electrophoretic mobility shift assays showed that dMi-2 thereby inhibits the DNA-binding activity of dDREF. Ectopic expression of dDREF and dMi-2 in eye imaginal discs resulted in severe and mild rough-eye phenotypes, respectively, whereas flies simultaneously expressing both proteins exhibited almost-normal eye phenotypes. Half-dose reduction of the dMi-2 gene enhanced the DREF-induced rough-eye phenotype. Immunostaining of polytene chromosomes of salivary glands showed that dDREF and dMi-2 bind in mutually exclusive ways. These lines of evidence define a novel function of dMi-2 in the negative regulation of dDREF by its DNA-binding activity. Finally, we postulated that dDREF and dMi-2 may demonstrate reciprocal regulation of their functions.

摘要

黑腹果蝇DNA复制相关元件(DRE)因子(dDREF)是一种转录调节因子,对于携带5'-TATCGATA DRE的基因的表达是必需的。据报道,dDREF可与染色质边界元件中的一个序列结合,因此,dDREF可能在调节绝缘子活性中发挥作用。为了进一步深入了解dDREF的功能,我们以DREF多肽为诱饵进行了酿酒酵母双杂交筛选,并鉴定出Mi-2是一种与DREF相互作用的蛋白。生化分析表明,果蝇Mi-2(dMi-2)的C末端区域特异性结合dDREF的DNA结合结构域。电泳迁移率变动分析表明,dMi-2由此抑制了dDREF的DNA结合活性。dDREF和dMi-2在眼成虫盘中的异位表达分别导致严重和轻度的粗糙眼表型,而同时表达这两种蛋白的果蝇表现出几乎正常的眼表型。dMi-2基因的半剂量减少增强了DREF诱导的粗糙眼表型。唾液腺多线染色体的免疫染色表明,dDREF和dMi-2以相互排斥的方式结合。这些证据确定了dMi-2通过其DNA结合活性对dDREF进行负调控的新功能。最后,我们推测dDREF和dMi-2可能表现出相互的功能调节。

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