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大鼠支链2-氧代酸脱氢酶激酶基因的结构组织及启动子调控区的部分特征分析

Structural organization of the rat branched-chain 2-oxo-acid dehydrogenase kinase gene and partial characterization of the promoter-regulatory region.

作者信息

Huang Y, Chuang D T

机构信息

Department of Biochemistry, University of Texas Southwestern Medical Center, Dallas 75235, USA.

出版信息

Biochem J. 1996 Jan 15;313 ( Pt 2)(Pt 2):603-9. doi: 10.1042/bj3130603.

Abstract

The gene encoding the rat branched-chain 2-oxo-acid dehydrogenase kinase (EC 2.7.1.115) has been isolated and partially characterized. The entire gene, including the promoter-regulatory region, spans 6 kb and contains 11 exons. The 5'-untranslated region comprising 264 bp is interrupted by intron 1 which is 581 bp in size. The complete in-frame sequence of intron 7 encodes the 49 amino acid insert previously reported to be present in the larger isoform of the rat kinase (Harris, Popov, Shimomura, Zhao, Jaskiewicz, Nanaumi and Suzuki (1992) Adv. Enzyme Regul. 32, 267-284). Sequencing of the 679 bp of the 5'-flanking region showed the absence of a canonical TATA box, similar to other branched-chain 2-oxo-acid dehydrogenase-complex genes. Several candidate cis-acting elements are present. These include CAAT boxes, Sp-1-binding sites, GCN-4 sites, CCAAT enhancer binding-protein sites (C/EBP) and glucocorticoid-responsive element (GRE) sites. Also present are a pair of direct repeats of unknown function. The luciferase-reporter assay showed that promoter activity is markedly higher in normal rat kidney (NRK-52E) cells than in rat hepatoma (FTO-2B) cells, and that the 5'-flanking region between bases -449 and +264 is both necessary and sufficient for basal transcription of the kinase gene.

摘要

编码大鼠支链2-氧代酸脱氢酶激酶(EC 2.7.1.115)的基因已被分离并进行了部分特性分析。整个基因,包括启动子调控区,跨度为6 kb,包含11个外显子。由264 bp组成的5'-非翻译区被大小为581 bp的内含子1中断。内含子7的完整读框序列编码先前报道的存在于大鼠激酶较大同工型中的49个氨基酸插入片段(哈里斯、波波夫、下村、赵、亚斯凯维茨、七并和铃木(1992年)《高级酶调节》32卷,267 - 284页)。对5'-侧翼区679 bp的测序显示,与其他支链2-氧代酸脱氢酶复合体基因类似,不存在典型的TATA框。存在几个候选顺式作用元件。这些元件包括CAAT框、Sp-1结合位点、GCN-4位点、CCAAT增强子结合蛋白位点(C/EBP)和糖皮质激素反应元件(GRE)位点。还存在一对功能未知的直接重复序列。荧光素酶报告基因检测表明,在正常大鼠肾(NRK-52E)细胞中启动子活性明显高于大鼠肝癌(FTO-2B)细胞,并且-449至+264碱基之间的5'-侧翼区对于激酶基因的基础转录既是必需的也是充分的。

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