首页> 外文期刊>Biochimica et biophysica acta. Gene structure and expression >Genomic cloning, mapping, structure and promoter analysis of HEADPIN, a serpin which is down-regulated in head and neck cancer cells
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Genomic cloning, mapping, structure and promoter analysis of HEADPIN, a serpin which is down-regulated in head and neck cancer cells

机译:HEADPIN(一种在头颈部癌细胞中被下调的丝氨酸蛋白酶抑制剂)的基因组克隆,作图,结构和启动子分析

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Headpin is a novel serine proteinase inhibitor (serpin) that is down-regulated in squamous cell carcinoma of the oral cavity and in squamous cell carcinoma cell lines of the head and neck. Using a panel of 18q21.3 YAC clones. We mapped and cloned the HEADPIN gene. The gene spans 10 kb and is composed of eight exons and seven introns. The genomic structure is identical with some other ovalbumin serpins (ov-serpins) in terms of the numbers, position and phasing of the intron/exon boundaries. HEADPIN was mapped within the serpin cluster in 18q21.3 between MASPIN and SCCA2 as follows: cen-MASPIN-HEADPIN-SCCA2-SCCAl-tel. The transcription start site was determined and the promoter activity of the 5'-flanking region was analyzed. Luciferase promoter assays in HaCaT cells showed that the -432 t -144 nucleotide region has functional promoter activity. The activity of the promoter/enhancer was not observed in head and neck cancer cell lines TU167 and UMSCCl which lack headpin expression. These data suggest that the differential expression of headpin in normal and carcinoma-derived cells is regulated at the transcriptional level. Understanding the genomic organization and transcriptional regulation of the ov-serpins clustered within 18q21.3 provides a critical framework for assessing their potential role in cancer.
机译:Headpin是一种新型的丝氨酸蛋白酶抑制剂(serpin),在口腔鳞状细胞癌和头颈部鳞状细胞癌细胞系中被下调。使用一组18q21.3 YAC克隆。我们定位并克隆了HEADPIN基因。该基因跨度为10 kb,由八个外显子和七个内含子组成。就内含子/外显子边界的数量,位置和定相而言,基因组结构与其他卵清蛋白丝氨酸蛋白酶抑制剂(ov-serpins)相同。 HEADPIN如下在MASPIN和SCCA2之间的18q21.3的serpin集群中进行了映射:cen-MASPIN-HEADPIN-SCCA2-SCCAl-tel。确定转录起始位点,并分析5'侧翼区的启动子活性。 HaCaT细胞中的萤光素酶启动子测定表明-432 t -144核苷酸区域具有功能性启动子活性。在缺乏头钉表达的头颈癌细胞系TU167和UMSC1中未观察到启动子/增强子的活性。这些数据表明headpin在正常细胞和癌衍生细胞中的差异表达在转录水平上受到调节。了解18q21.3中聚集的ov-serpins的基因组组织和转录调控为评估其在癌症中的潜在作用提供了关键框架。

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