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利用大肠杆菌uidA基因作为沃氏甲烷球菌中的报告基因,用于分析编码无硒氢化酶的操纵子之间基因间区域的调控功能。

Use of the Escherichia coli uidA gene as a reporter in Methanococcus voltae for the analysis of the regulatory function of the intergenic region between the operons encoding selenium-free hydrogenases.

作者信息

Beneke S, Bestgen H, Klein A

机构信息

Department of Biology, Philipps-University, Marburg, Germany.

出版信息

Mol Gen Genet. 1995 Jul 28;248(2):225-8. doi: 10.1007/BF02190804.

Abstract

The Escherichia coli beta-glucuronidase gene uidA was linked to a region of the Methanococcus voltae genome containing the putative promoter of a gene for a DNA-binding protein and introduced into the M. voltae chromosome. It was found that the enzyme was expressed in the cells in easily measurable amounts. The reporter gene was then placed under the control of the intergenic region found between two divergently transcribed gene groups encoding selenium-free hydrogenases, which are measurably transcribed only after selenium depletion. This region is supposed not only to contain the divergent promoters governing the transcription of the hydrogenase genes but also cis regulatory elements necessary for the negative transcriptional regulation in which selenium is involved. It was shown that the intergenic region functioned as a promoter region for the reporter gene in either orientation. The additional finding that beta-glucuronidase expression was dependent on selenium depletion localizes the cis regulatory elements to the intergenic region between the two hydrogenase operons.

摘要

大肠杆菌β-葡萄糖醛酸酶基因uidA与沃氏甲烷球菌基因组的一个区域相连,该区域包含一种DNA结合蛋白基因的假定启动子,并被导入到沃氏甲烷球菌染色体中。结果发现,该酶在细胞中以易于测量的量表达。然后,将报告基因置于两个反向转录的无硒氢化酶基因簇之间的基因间区域的控制之下,这两个基因簇只有在硒耗尽后才会有可测量的转录。该区域不仅被认为包含控制氢化酶基因转录的反向启动子,还包含硒参与的负转录调控所必需的顺式调控元件。结果表明,该基因间区域在任一方向上都作为报告基因的启动子区域发挥作用。β-葡萄糖醛酸酶表达依赖于硒耗尽这一额外发现,将顺式调控元件定位到了两个氢化酶操纵子之间的基因间区域。

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