首页> 美国卫生研究院文献>The Journal of Clinical Investigation >The human 230-kD bullous pemphigoid antigen gene (BPAG1). Exon-intron organization and identification of regulatory tissue specific elements in the promoter region.
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The human 230-kD bullous pemphigoid antigen gene (BPAG1). Exon-intron organization and identification of regulatory tissue specific elements in the promoter region.

机译:人类230 kD大疱性类天疱疮抗原基因(BPAG1)。外显子-内含子组织和启动子区域中调控组织特异性元件的鉴定。

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摘要

The 230-kD bullous pemphigoid antigen (BPAG1), a hemidesmosomal protein, is encoded by a gene at the human chromosomal locus 6p11-12. We have elucidated the exon-intron organization of the entire human BPAG1 gene, including approximately 2.6 kb of 5'-flanking DNA. Seven overlapping genomic clones, spanning approximately 20 kb, contained the entire approximately 9 kb coding sequence of BPAG1 and consisted of 22 separate exons, which varied from 78 to 2,810 bp in size. The 5' flanking region of DNA, upstream from the ATG initiation codon for translation, was found to contain several putative transcriptional response elements. Most interestingly, two motifs potentially conferring keratinocyte specific expression to the gene were detected. The presence of such elements was suggested by approximately 20-fold higher expression of a promoter/chloramphenicol acetyl transferase (CAT) construct in normal human epidermal keratinocytes that express the endogenous gene, as compared to several non-expressing cell types. Transient transfections with 5'-deletion clones of the promoter/reporter gene (CAT) constructs identified a region containing a putative tissue specific element, KRE2, which also conferred tissue specificity to the expression of the truncated promoter downstream from this element, however, a mutated derivative of KRE2 was not functional. Detailed knowledge of the structure and regulation of the BPAG1 gene will aid in further elucidation of diseases affecting the cutaneous basement membrane zone.
机译:230 kD大疱性类天疱疮抗原(BPAG1)是一种半染色体蛋白质,由人染色体基因座6p11-12处的一个基因编码。我们已经阐明了整个人类BPAG1基因的外显子-内含子组织,包括大约2.6 kb的5'侧翼DNA。七个大约20 kb的重叠基因组克隆包含BPAG1的大约9 kb整个编码序列,由22个独立的外显子组成,大小从78到2810 bp不等。发现在用于翻译的ATG起始密码子上游的DNA的5'侧翼区含有几个假定的转录反应元件。最有趣的是,检测到两个可能赋予该基因角质形成细胞特异性表达的基序。与几种非表达细胞类型相比,在表达内源基因的正常人表皮角质形成细胞中,启动子/氯霉素乙酰转移酶(CAT)构建体的表达高约20倍,表明了此类元素的存在。用启动子/报告基因(CAT)构建体的5'缺失克隆进行瞬时转染,鉴定出一个区域,该区域包含一个假定的组织特异性元件KRE2,该区域还赋予该组织下游截短的启动子表达的组织特异性。 KRE2的突变衍生物不起作用。 BPAG1基因的结构和调控的详细知识将有助于进一步阐明影响皮肤基底膜区域的疾病。

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