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本文引用的文献

1
Developmental expression of maf-1 messenger ribonucleic acids in rat kidney by in situ hybridization histochemistry.通过原位杂交组织化学法检测大鼠肾脏中maf-1信使核糖核酸的发育表达。
Biochem Biophys Res Commun. 2000 Jun 16;272(3):777-82. doi: 10.1006/bbrc.2000.2865.
2
Maf transcriptionally activates the mouse p53 promoter and causes a p53-dependent cell death.Maf通过转录激活小鼠p53启动子并导致p53依赖的细胞死亡。
J Biol Chem. 2000 Jun 16;275(24):17991-9. doi: 10.1074/jbc.M000921200.
3
Molecular cloning and functional characterization of the mouse mafB gene.小鼠mafB基因的分子克隆与功能特性分析
Gene. 2000 Jan 25;242(1-2):419-26.
4
Regulation of mouse lens fiber cell development and differentiation by the Maf gene.Maf基因对小鼠晶状体纤维细胞发育和分化的调控
Development. 2000 Jan;127(2):307-17. doi: 10.1242/dev.127.2.307.
5
c-Maf induces monocytic differentiation and apoptosis in bipotent myeloid progenitors.c-Maf诱导双能髓系祖细胞向单核细胞分化并凋亡。
Blood. 1999 Sep 1;94(5):1578-89.
6
Pax6 induces ectopic eyes in a vertebrate.Pax6在脊椎动物中诱导异位眼的形成。
Development. 1999 Oct;126(19):4213-22. doi: 10.1242/dev.126.19.4213.
7
Regulation of lens fiber cell differentiation by transcription factor c-Maf.转录因子c-Maf对晶状体纤维细胞分化的调控
J Biol Chem. 1999 Jul 2;274(27):19254-60. doi: 10.1074/jbc.274.27.19254.
8
Requirement for the c-Maf transcription factor in crystallin gene regulation and lens development.晶体蛋白基因调控及晶状体发育中c-Maf转录因子的需求
Proc Natl Acad Sci U S A. 1999 Mar 30;96(7):3781-5. doi: 10.1073/pnas.96.7.3781.
9
Dual roles for Pax-6: a transcriptional repressor of lens fiber cell-specific beta-crystallin genes.Pax-6的双重作用:晶状体纤维细胞特异性β-晶状体蛋白基因的转录抑制因子。
Mol Cell Biol. 1998 Sep;18(9):5579-86. doi: 10.1128/MCB.18.9.5579.
10
Frequent dysregulation of the c-maf proto-oncogene at 16q23 by translocation to an Ig locus in multiple myeloma.在多发性骨髓瘤中,16q23处的c-maf原癌基因常因易位至免疫球蛋白(Ig)基因座而发生失调。
Blood. 1998 Jun 15;91(12):4457-63.

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.

DOI:10.1093/nar/29.5.1228
PMID:11222774
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC29716/
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。