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大肠杆菌单链结合蛋白基因调控区的分析

Analysis of the regulatory region of the ssb gene of Escherichia coli.

作者信息

Brandsma J A, Bosch D, de Ruÿter M, van de Putte P

出版信息

Nucleic Acids Res. 1985 Jul 25;13(14):5095-109. doi: 10.1093/nar/13.14.5095.

Abstract

The regulation of the ssb gene of E. coli has been studied. We reported earlier that the SOS box of the neighbouring uvrA gene also controls the transcription of the ssb gene. Detailed analysis of the upstream region of ssb by S1 mapping reveals the existence of three in vivo functional promoters of which the most upstream one (PI) is inducible by DNA damage. Measurement of galactokinase synthesis using galK fusion plasmids indicates that the uninduced level of transcription from the PI promoter is low. Ssb multicopy plasmids lacking the PI promoter still complement the UV sensitivity of an Ssb mutant. The role of the three promoters in the regulation of the level of Ssb protein in the cell, is discussed.

摘要

对大肠杆菌单链结合蛋白(SSB)基因的调控进行了研究。我们之前报道过,相邻的uvrA基因的SOS框也控制着SSB基因的转录。通过S1图谱对SSB上游区域进行详细分析,发现存在三个体内功能性启动子,其中最上游的一个(P1)可被DNA损伤诱导。使用半乳糖激酶融合质粒测量半乳糖激酶的合成表明,P1启动子未诱导时的转录水平较低。缺乏P1启动子的SSB多拷贝质粒仍能弥补SSB突变体对紫外线的敏感性。文中讨论了这三个启动子在细胞中SSB蛋白水平调控中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6250/321852/78df6815c7cc/nar00308-0099-a.jpg

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