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The identification of Hoxc8 target genes

机译:Hoxc8靶基因的鉴定

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摘要

Hox genes encode transcription factors that control spatial patterning during embryogenesis. To date, downstream targets of Hox genes have proven difficult to identify. Here, we describe studies designed to identify target genes under the control of the murine transcription factor Hoxc8. We used a mouse 16,463 gene oligonucleotide microarray to identify mRNAs whose expression was altered by the overexpression of Hoxc8 in C57BL/6J mouse embryo fibroblasts (MEF) in cell culture (in vitro). We identified a total of 34 genes whose expression was changed by 2-fold or greater: 16 genes were up-regulated, and 18 genes were down-regulated. The majority of genes encoded proteins involved in critical biological processes, such as cell adhesion, migration, metabolism, apoptosis, and tumorigenesis. Two genes showed high levels of regulation: (ⅰ) secreted phosphoprotein 1 (Spp1), also known as osteopontin {OPN). was down-regulated 4.8-fold, and (ⅱ) frizzled homolog 2 (Drosophila) (Fzd2) was up-regulated 4.4-fold. Chromatin immunoprecipitation (Chip) analysis confirmed the direct interaction between the OPN promoter and Hoxc8 protein in vivo, supporting the view that OPN is a direct transcriptional target of Hoxc8.
机译:Hox基因编码在胚胎发生过程中控制空间模式的转录因子。迄今为止,已证明难以鉴定Hox基因的下游靶标。在这里,我们描述了旨在在鼠转录因子Hoxc8的控制下识别目标基因的研究。我们使用小鼠16,463基因寡核苷酸微阵列来鉴定mRNA,其表达因细胞培养(体外)的C57BL / 6J小鼠胚胎成纤维细胞(MEF)中Hoxc8的过表达而改变。我们鉴定了总共34个基因,它们的表达变化了2倍或更多:16个基因被上调,而18个基因被下调。大多数基因编码参与关键生物学过程的蛋白质,例如细胞粘附,迁移,代谢,细胞凋亡和肿瘤发生。两个基因显示出高水平的调节作用:(:)分泌的磷蛋白1(Spp1),也称为骨桥蛋白(OPN)。下调了4.8倍,(ⅱ)卷曲的同源物2(果蝇)(Fzd2)上调了4.4倍。染色质免疫沉淀(Chip)分析证实了OPN启动子和Hoxc8蛋白在体内的直接相互作用,支持了OPN是Hoxc8的直接转录靶标的观点。

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