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人甲状旁腺激素相关肽基因上游启动子的鉴定

Identification of an up-stream promoter of the human parathyroid hormone-related peptide gene.

作者信息

Mangin M, Ikeda K, Dreyer B E, Broadus A E

机构信息

Department of Internal Medicine, Yale University, New Haven, Connecticut 06510.

出版信息

Mol Endocrinol. 1990 Jun;4(6):851-8. doi: 10.1210/mend-4-6-851.

DOI:10.1210/mend-4-6-851
PMID:2233743
Abstract

Previous evidence has suggested that the human PTH-related peptide (PTHRP) gene uses two promoters, one a short down-stream element lying immediately between two 5' exons (1 and 2) and a second lying in an unknown up-stream location. We approached identification of the up-stream element in three steps. First, Northern analysis carried out using progressively 5' fragments of the gene as probes identified a candidate region some 2.5 kilobases up-stream of exon 1. Second, a battery of overlapping 5' cRNA probes was used in RNase protection experiments to identify two previously unrecognized exons, 212 and 93 basepairs in length (termed exons 1A and 1B to distinguish them from the previously designated exon 1, which was termed exon 1C). Third, primer extension experiments were performed with oligonucleotides complementary to each of the 5' exonic sequences. These experiments identified a transcription start site up-stream of exon 1A and also demonstrated that the 5' exons of the PTHRP gene could be spliced together in several combinations. The up-stream promoter element contains a TATA box, but does not otherwise resemble the down-stream PTHRP gene promoter or the PTH gene promoter. We conclude that the human PTHRP gene contains eight exons spanning more than 15 kilobases of genomic DNA, with promoter elements lying immediately up-stream of exons 1A and 2. The identification of these elements will permit functional analysis of their roles in mediating tissue- and tumor-specific PTHRP gene expression.

摘要

先前的证据表明,人类甲状旁腺激素相关肽(PTHRP)基因使用两个启动子,一个是位于两个5'外显子(1和2)之间紧邻的短下游元件,另一个位于未知的上游位置。我们分三步来确定上游元件。首先,使用该基因逐渐向5'端的片段作为探针进行Northern分析,确定了外显子1上游约2.5千碱基的一个候选区域。其次,一系列重叠的5' cRNA探针用于核糖核酸酶保护实验,以确定两个先前未识别的外显子,长度分别为212和93个碱基对(称为外显子1A和1B,以区别于先前指定的外显子1,后者称为外显子1C)。第三,用与每个5'外显子序列互补的寡核苷酸进行引物延伸实验。这些实验确定了外显子1A上游的一个转录起始位点,还证明了PTHRP基因的5'外显子可以以几种组合方式拼接在一起。上游启动子元件含有一个TATA盒,但在其他方面与下游PTHRP基因启动子或PTH基因启动子不同。我们得出结论,人类PTHRP基因包含八个外显子,跨越超过15千碱基的基因组DNA,启动子元件位于外显子1A和2的紧邻上游。这些元件的确定将有助于对它们在介导组织和肿瘤特异性PTHRP基因表达中的作用进行功能分析。

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引用本文的文献

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