人类癌细胞中两种fas相关磷酸酶-1启动子的鉴定

S. Irie, Yin Li, H. Kanki, Tomoko Ohyama, L. Deaven, Stefan Someo, Taka-Aki Sato
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引用次数: 22

摘要

fas相关磷酸酶-1 (Fas-associated phosphatase-1, FAP-1)已被报道为人类癌细胞中fas介导的信号转导的负调节因子。为了深入了解FAP-1基因的潜在致癌作用,我们研究了其在正常细胞和癌细胞中的转录调控。为了鉴定FAP-1启动子序列,我们首先利用cDN - A末端5 '快速扩增产物(5 ' -RACE)作为探针,分离出含有FAP-1基因上游调控区域的PI和cosmid克隆。阳性克隆的基因组分析显示,在所有测试的人类癌细胞系中,主要的FAP-1 mRNA都是从其近端启动子(pPRM)转录的,但在人类结肠癌细胞系DLD-1中发现了一个来自其远端启动子(dPRM)的大转录本。这表明FAP-1基因可能在某些类型的人类癌症中异常失调,包括结肠癌。对FAP-1基因上游区域的序列分析强烈提示,FAP-1基因的转录可能受到多种转录调控元件的控制,包括其2个启动子中的NF-κB、NF- il6和p53。这些结果提示,在人类癌症中,FAP-1基因可能是重要的细胞凋亡相关核因子调控的靶基因。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Identification of Two Fas-Associated Phosphatase-1 (FAP-1) Promoters in Human Cancer Cells
Fas-associated phosphatase-1 (FAP-1) has been reported as a negative regulator of Fas-mediated signal transduction in human cancer cells. To obtain insights into the potential carcinogenesis of the FAP-1 gene, we investigated its transcriptional regulation in normal and cancerous cells. To identify the FAP-1 promoter sequences, we first isolated PI and cosmid clones that contained the regulatory region upstream from the FAP-1 gene by using the PCR products of 5′ rapid amplification of cDN A end (5′-RACE) as probes. Genomic analysis of positive clones revealed that the major FAP-1 mRNA was transcribed from its proximal promoter (pPRM) in all human cancer cell lines tested, but 1 additional large transcript derived from its distal promoter (dPRM) was found in the human colon cancer cell line DLD-1. This suggests that the FAP-1 gene may be aberrantly dysregulated in some types of human cancers, including colon carcinoma. Sequence analysis of the region upstream from the FAP-1 gene strongly suggests that the transcript of the FAP-1 gene may be controlled by a variety of transcriptional regulatory elements, including NF-κB, NF-IL6, and p53 in its 2 promoters. These results imply that the FAP-1 gene may be a target gene under the control of important apoptosis-related nuclear factors in human cancers.
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