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人类内皮素-B受体基因。结构组织与染色体定位。

The human endothelin-B receptor gene. Structural organization and chromosomal assignment.

作者信息

Arai H, Nakao K, Takaya K, Hosoda K, Ogawa Y, Nakanishi S, Imura H

机构信息

Department of Medicine, Kyoto University School of Medicine, Japan.

出版信息

J Biol Chem. 1993 Feb 15;268(5):3463-70.

PMID:8429023
Abstract

The gene encoding the human endothelin-B receptor (hET-BR) has been isolated, and its structural organization and chromosomal assignment have been determined. Southern blot analysis demonstrated a single copy of the hET-BR gene in the human genome. The hET-BR gene spans 24 kilobases and consists of seven exons and six introns. The size range for exons is 109-2855 base pairs, although that for introns is 0.2-14.5 kilobases. Every intron occurs near the border of the putative transmembrane domain in the coding region. The major transcription initiation sites were mapped to the positions 258 and 229 base pairs upstream of the ATG initiation codon by primer extension and nuclease S1 protection experiments. The 5'-flanking region of the hET-BR gene lacks conventional TATA and CCAAT boxes but contains a sequence of potential Sp1 binding sites upstream of the transcription initiation sites. There are some canonical consensus sequences of cis-elements including GATA motif, acute phase reactant regulatory element, and E box. Using human-rodent somatic hybrid cell lines, the hET-BR gene was assigned to human chromosome 13. The present study will lead to a better understanding of the mechanism for the transcriptional regulation of the hET-BR gene and will give a clue as to how to search for possible genetic disorders of hET-BR.

摘要

编码人内皮素 - B受体(hET - BR)的基因已被分离出来,并且其结构组织和染色体定位也已确定。Southern印迹分析表明,hET - BR基因在人类基因组中为单拷贝。hET - BR基因跨度为24千碱基,由7个外显子和6个内含子组成。外显子的大小范围是109 - 2855个碱基对,而内含子的大小范围是0.2 - 14.5千碱基。每个内含子都出现在编码区推定跨膜结构域的边界附近。通过引物延伸和核酸酶S1保护实验,主要转录起始位点被定位到ATG起始密码子上游258和229个碱基对的位置。hET - BR基因的5'侧翼区域缺乏传统的TATA和CCAAT框,但在转录起始位点上游含有一系列潜在的Sp1结合位点。存在一些顺式元件的典型共有序列,包括GATA基序、急性期反应物调节元件和E框。利用人 - 啮齿动物体细胞杂交细胞系,hET - BR基因被定位到人类13号染色体上。本研究将有助于更好地理解hET - BR基因转录调控的机制,并为如何寻找hET - BR可能的遗传疾病提供线索。

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