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大鼠γ-谷氨酰转移酶基因的克隆与分析

Cloning and analysis of the rat gamma-glutamyltransferase gene.

作者信息

Rajagopalan S, Park J H, Patel P D, Lebovitz R M, Lieberman M W

机构信息

Department of Pathology, Baylor College of Medicine, Houston, Texas 77030.

出版信息

J Biol Chem. 1990 Jul 15;265(20):11721-5.

PMID:1973164
Abstract

We have isolated and characterized a complete structural gene encoding the enzyme gamma-glutamyltransferase ((5-glutamyl)-peptide:amino acid 5-glutamyltransferase; EC 2.3.2.2). The gene contains 8 exons and spans approximately 12 kilobases. Ras-transformed rat liver epithelial cells and rat kidney express RNAs which differ in length by approximately 0.3 kilobase pair. Comparison of the genomic sequence with kidney gamma GT cDNA sequence indicates that the first exon is noncoding, and nuclease protection and primer extension data have identified a potential kidney transcription start site (defined as +1) for this exon. The site is not associated with a TATA box, but there are two CCAAT boxes (-136 and -599) and two sites (-101 and -746) containing the consensus sequences to which the transcription factor SP1 is known to bind. There is also a sequence at -453 (TGTGGTTG) that is highly homologous to the core sequence (TGTGG(T)3-5G) of SV40 and polyoma viral enhancers.

摘要

我们已经分离并鉴定了一个编码γ-谷氨酰转移酶((5-谷氨酰)-肽:氨基酸5-谷氨酰转移酶;EC 2.3.2.2)的完整结构基因。该基因包含8个外显子,跨度约为12千碱基。经Ras转化的大鼠肝上皮细胞和大鼠肾脏表达的RNA,其长度相差约0.3千碱基对。基因组序列与肾脏γ-谷氨酰转移酶cDNA序列的比较表明,第一个外显子是非编码的,核酸酶保护和引物延伸数据已确定该外显子的一个潜在肾脏转录起始位点(定义为+1)。该位点与TATA框无关,但有两个CCAAT框(-136和-599)以及两个含有已知转录因子SP1结合的共有序列的位点(-101和-746)。在-453处还有一个序列(TGTGGTTG),它与SV40和多瘤病毒增强子的核心序列(TGTGG(T)3-5G)高度同源。

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