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人尿嘧啶-DNA糖基化酶基因的结构及启动子功能分析。

Structure of the gene for human uracil-DNA glycosylase and analysis of the promoter function.

作者信息

Haug T, Skorpen F, Lund H, Krokan H E

机构信息

UNIGEN Center for Molecular Biology, University of Trondheim, Norway.

出版信息

FEBS Lett. 1994 Oct 17;353(2):180-4. doi: 10.1016/0014-5793(94)01042-0.

Abstract

The gene for human uracil-DNA glycosylase (UNG) contains 4 exons and has an approximate size of 13 kb. The promoter is very GC rich and lacks a TATA box. Nested deletions of the promoter demonstrated that two SP1 elements and a putative c-MYC element proximal to the transcription initiation region were sufficient to support some 27% of the promoter activity, while a clone that in addition contained the elements E2F/SP1/CCAAT increased expression to almost 90% of the full-length construct. A region upstream of these elements appears to exert a negative control function.

摘要

人类尿嘧啶-DNA糖基化酶(UNG)基因包含4个外显子,大小约为13 kb。其启动子富含GC且缺乏TATA框。对启动子进行嵌套缺失实验表明,转录起始区域近端的两个SP1元件和一个假定的c-MYC元件足以支持约27%的启动子活性,而一个额外包含E2F/SP1/CCAAT元件的克隆可使表达增加至全长构建体的近90%。这些元件上游的一个区域似乎发挥着负调控功能。

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