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果蝇Mes4基因作为转录因子DREF的一个新靶点的鉴定。

Identification of the Drosophila Mes4 gene as a novel target of the transcription factor DREF.

作者信息

Suyari Osamu, Ida Hiroyuki, Yoshioka Yasuhide, Kato Yasuko, Hashimoto Reina, Yamaguchi Masamitsu

机构信息

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

出版信息

Exp Cell Res. 2009 May 1;315(8):1403-14. doi: 10.1016/j.yexcr.2008.12.017. Epub 2009 Jan 3.

DOI:10.1016/j.yexcr.2008.12.017
PMID:19150446
Abstract

The Mes4 gene has been identified as one of the maternal Dorsal target genes in Drosophila. In the present study, we found a DNA replication-related element (DRE, 5'-TATCGATA) in the Mes4 promoter recognized by the DRE-binding factor (DREF). Luciferase transient expression assays in S2 cells using Mes4 promoter-luciferase fusion plasmids revealed that the DRE sequence is essential for Mes4 promoter activity. Requirement of DRE for Mes4 promoter activity was further confirmed by anti-beta-galactosidase antibody-staining of various tissues from transgenic flies carrying Mes4 promoter-lacZ fusion genes. Furthermore, wild type Mes4 promoter activity was decreased by 40% in DREF-depleted S2 cells. These results indicate that DREF positively regulates Mes4 gene expression. Band mobility shift analyses using Kc cell nuclear extracts further indicated that the DRE sequence in the Mes4 promoter is especially important for binding to DREF. Moreover, specific binding of DREF to the involved genomic region could be demonstrated by chromatin immunoprecipitation assays using anti-DREF antibodies. These results, taken together, indicate that the DRE/DREF system activates transcription of the Mes4 gene. In addition, knockdown of the Mes4 gene in wing imaginal discs using the GAL4-UAS system caused an atrophied wing phenotype, suggesting that Mes4 is required for wing morphogenesis.

摘要

Mes4基因已被确定为果蝇中母体背侧靶基因之一。在本研究中,我们在Mes4启动子中发现了一个与DNA复制相关的元件(DRE,5'-TATCGATA),它可被DRE结合因子(DREF)识别。使用Mes4启动子-荧光素酶融合质粒在S2细胞中进行的荧光素酶瞬时表达分析表明,DRE序列对Mes4启动子活性至关重要。携带Mes4启动子-lacZ融合基因的转基因果蝇各种组织的抗β-半乳糖苷酶抗体染色进一步证实了DRE对Mes4启动子活性的需求。此外,在缺乏DREF的S2细胞中,野生型Mes4启动子活性降低了40%。这些结果表明,DREF正向调节Mes4基因表达。使用Kc细胞核提取物进行的凝胶迁移率变动分析进一步表明,Mes4启动子中的DRE序列对于与DREF结合尤为重要。此外,使用抗DREF抗体的染色质免疫沉淀分析可以证明DREF与相关基因组区域的特异性结合。综上所述,这些结果表明DRE/DREF系统激活Mes4基因的转录。此外,使用GAL4-UAS系统在翅成虫盘中敲低Mes4基因会导致翅萎缩表型,这表明Mes4是翅形态发生所必需的。

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