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230kDa大疱性类天疱疮抗原基因(BPAG1)的组织特异性表达。一种新型角质形成细胞调节顺式元件KRE3的鉴定。

Tissue-specific expression of the 230-kDa bullous pemphigoid antigen gene (BPAG1). Identification of a novel keratinocyte regulatory cis-element KRE3.

作者信息

Tamai K, Silos S A, Li K, Korkeela E, Ishikawa H, Uitto J

机构信息

Department of Dermatology, Jefferson Medical College, Thomas Jefferson University, Philadelphia, Pennsylvania 19107, USA.

出版信息

J Biol Chem. 1995 Mar 31;270(13):7609-14. doi: 10.1074/jbc.270.13.7609.

Abstract

The 230-kDa bullous pemphigoid antigen gene (BPAG1) is expressed exclusively in basal keratinocytes of epidermis. In this study, we have identified a novel cis-element, keratinocyte responsive element 3 (KRE3), at position -216 to -197 of the human BPAG1 gene. A promoter-CAT construct containing this element had approximately 50-fold higher expression than a similar construct devoid of this sequence when tested in transient transfections of cultured human keratinocytes. However, there was no effect on the low base-line level of expression in cultured skin fibroblasts. KRE3 contains a palindromic sequence 5'-CAAATATTTG-3', and mutations in this sequence significantly reduced the promoter activity. Gel mobility shift assays with an oligomer containing KRE3 sequence demonstrated binding activity with nuclear proteins isolated from keratinocytes. One of the DNA/protein complexes was clearly specific, since competition with > 12.5-fold excess of the unlabeled oligomer resulted in disappearance of this band. No specific binding activity was noted with nuclear proteins extracted from fibroblasts. Thus, KRE3 appears to serve as the binding site for keratinocyte-specific trans-activating factor(s), and KRE3 may thus confer the tissue-specific expression to the BPAG1 gene.

摘要

230kDa的大疱性类天疱疮抗原基因(BPAG1)仅在表皮的基底角质形成细胞中表达。在本研究中,我们在人BPAG1基因的-216至-197位鉴定出一个新的顺式元件,即角质形成细胞反应元件3(KRE3)。当在培养的人角质形成细胞的瞬时转染中进行测试时,含有该元件的启动子-CAT构建体的表达比缺乏该序列的类似构建体高约50倍。然而,对培养的皮肤成纤维细胞中低基线表达水平没有影响。KRE3含有回文序列5'-CAAATATTTG-3',该序列中的突变显著降低了启动子活性。用含有KRE3序列的寡聚物进行凝胶迁移率变动分析表明,其与从角质形成细胞中分离的核蛋白具有结合活性。其中一种DNA/蛋白质复合物明显具有特异性,因为与超过12.5倍过量的未标记寡聚物竞争导致该条带消失。从成纤维细胞中提取的核蛋白未观察到特异性结合活性。因此,KRE3似乎作为角质形成细胞特异性反式激活因子的结合位点,并且KRE3可能因此赋予BPAG1基因组织特异性表达。

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