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Pax6对培养细胞中c-maf基因表达的调控。

Regulation of c-maf gene expression by Pax6 in cultured cells.

作者信息

Sakai M, Serria M S, Ikeda H, Yoshida K, Imaki J, Nishi S

机构信息

Department of Biochemistry and Department of Ophthalmology, Hokkaido University School of Medicine, N15, W7, Kita-ku, Sapporo 060-8638, Japan.

出版信息

Nucleic Acids Res. 2001 Mar 1;29(5):1228-37. doi: 10.1093/nar/29.5.1228.

Abstract

c-Maf is a bZip transcription factor expressed in developmental and cellular differentiation processes. Recently, a c-maf knockout mouse model, showing abnormal lens development, has been reported. In order to study the regulation mechanisms of c-maf gene expression during the differentiation process we have cloned and functionally characterized the rat c-maf (maf-2) gene. The rat c-maf gene is an intronless gene, covering a length of 3.5 kb. Transient transfection analysis of the 5'-flanking region of the c-maf gene using luciferase as the reporter gene shows that Pax6, a master transcription factor for lens development, strongly activates the c-maf promoter construct. Endogenous c-maf is also activated by the Pax6 expression vector. Electrophoresis mobility shift assay and DNase I footprinting analysis show that at least three Pax6-binding sites are located in the 5'-flanking and 5'-non-coding regions of the rat c-maf gene. The c-maf gene was also markedly activated by its own product, c-Maf, through the MARE (Maf recognition element), suggesting that a positive autoregulatory mechanism controls this gene. In situ hybridization histochemical detection of Pax6 and c-Maf in the E14 lens showed that both mRNAs are expressed in the lens equator where lens epithelial cells are differentiating to lens fiber cells. These results suggest that a Pax6/c-Maf transcription factor cascade is working in lens development.

摘要

c-Maf是一种在发育和细胞分化过程中表达的bZip转录因子。最近,有报道称一种c-maf基因敲除小鼠模型表现出晶状体发育异常。为了研究c-maf基因在分化过程中的表达调控机制,我们克隆了大鼠c-maf(maf-2)基因并对其进行了功能鉴定。大鼠c-maf基因是一个无内含子基因,长度为3.5 kb。以荧光素酶为报告基因对c-maf基因的5'侧翼区域进行瞬时转染分析表明,晶状体发育的主要转录因子Pax6强烈激活c-maf启动子构建体。内源性c-maf也被Pax6表达载体激活。电泳迁移率变动分析和DNase I足迹分析表明,大鼠c-maf基因的5'侧翼和5'非编码区域至少有三个Pax6结合位点。c-maf基因也通过MARE(Maf识别元件)被其自身产物c-Maf显著激活,这表明一种正向自调节机制控制着该基因。对E14期晶状体中Pax6和c-Maf进行原位杂交组织化学检测表明,两种mRNA均在晶状体赤道区表达,此处晶状体上皮细胞正在分化为晶状体纤维细胞。这些结果表明,Pax6/c-Maf转录因子级联反应在晶状体发育中起作用。

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