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兔分化依赖性K3角蛋白基因的一段300bp 5'-上游序列可作为角质形成细胞特异性启动子。

A 300 bp 5'-upstream sequence of a differentiation-dependent rabbit K3 keratin gene can serve as a keratinocyte-specific promoter.

作者信息

Wu R L, Galvin S, Wu S K, Xu C, Blumenberg M, Sun T T

机构信息

Ronald O. Perelman Department of Dermatology, New York University Medical School 10016.

出版信息

J Cell Sci. 1993 Jun;105 ( Pt 2):303-16. doi: 10.1242/jcs.105.2.303.

Abstract

Keratinocytes of the suprabasal compartment of many stratified epithelia synthesize as a major differentiation product a keratin pair, consisting of an acidic and a basic keratin, which accounts for 10-20% of the newly synthesized proteins. While genes of several differentiation-related keratins have been cloned and studied, relatively little is known about the molecular basis underlying their tissue-specific and differentiation-dependent expression. We have chosen to study, as a prototype of these genes, the gene of K3 keratin, which has the unique property of being expressed in the majority of corneal epithelial basal cells but suprabasally in peripheral cornea, the site of corneal epithelial stem cells. Using a monoclonal antibody, AE5, specific for K3 keratin, and a fragment of human K3 gene as probes, we have isolated several cDNA and genomic clones of rabbit K3 keratin. One genomic clone has been sequenced and characterized, and the identity of its coding sequence with that of cDNAs indicates that it corresponds to the single, functional rabbit K3 gene. Transfection assays showed that its 3.6 kb 5'-upstream sequence can drive a chloramphenicol acetyl transferase (CAT) reporter gene to express in cultured corneal and esophageal epithelial cells, but not in mesothelial and kidney epithelial cells or fibroblasts, all of rabbit origin. Serial deletion experiments narrowed this keratinocyte-specific promoter to within -300 bp upstream of the transcription initiation site. Its activity is not regulated by the coding or 3'-noncoding sequences that have been tested so far. This 300 bp 5'-upstream sequence of K3 keratin gene, which can function in vitro as a keratinocyte-specific promoter, contains two clusters of partially overlapping motifs, one with an NFkB consensus sequence and another with a GC box. The combinatorial effects of these multiple motifs and their cognate binding proteins may play an important role in regulating the expression of this tissue-restricted and differentiation-dependent keratin gene.

摘要

许多复层上皮的基底层以上部分的角质形成细胞合成一种主要的分化产物——角蛋白对,它由一种酸性角蛋白和一种碱性角蛋白组成,占新合成蛋白质的10% - 20%。虽然几个与分化相关的角蛋白基因已被克隆和研究,但关于其组织特异性和分化依赖性表达的分子基础所知甚少。作为这些基因的一个原型,我们选择研究K3角蛋白基因,它具有独特的特性,即在大多数角膜上皮基底细胞中表达,但在角膜上皮干细胞所在的周边角膜的基底层以上部分表达。利用一种对K3角蛋白特异的单克隆抗体AE5和人K3基因的一个片段作为探针,我们分离出了兔K3角蛋白的几个cDNA和基因组克隆。对一个基因组克隆进行了测序和鉴定,其编码序列与cDNA的编码序列相同,表明它对应于单个有功能的兔K3基因。转染实验表明,其3.6 kb的5'上游序列可驱动氯霉素乙酰转移酶(CAT)报告基因在培养的兔角膜和食管上皮细胞中表达,但在间皮细胞、肾上皮细胞或成纤维细胞中不表达。系列缺失实验将这个角质形成细胞特异性启动子定位到转录起始位点上游- 300 bp范围内。到目前为止,其活性不受已测试的编码序列或3'非编码序列的调控。K3角蛋白基因的这个300 bp 5'上游序列在体外可作为角质形成细胞特异性启动子发挥作用,它包含两簇部分重叠的基序,一簇带有NFκB共有序列,另一簇带有GC盒。这些多个基序及其相关结合蛋白的组合效应可能在调节这个组织限制性和分化依赖性角蛋白基因的表达中起重要作用。

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