Suppr超能文献

编码聚腺苷酸聚合酶I的大肠杆菌pcnB(质粒拷贝数)基因启动子区域的转录起始位点。

Transcription start sites in the promoter region of the Escherichia coli pcnB (plasmid copy number) gene coding for poly(A) polymerase I.

作者信息

Jasiecki Jacek, Wegrzyn Grzegorz

机构信息

Department of Molecular Biology, University of Gdańsk, Kładki 24, 80-822 Gdańsk, Poland.

出版信息

Plasmid. 2006 Mar;55(2):169-72. doi: 10.1016/j.plasmid.2005.10.002. Epub 2005 Dec 2.

Abstract

Escherichia coli pcnB gene was discovered as a regulator of ColE1 plasmid copy number about 20 years ago. Further studies indicated that this gene codes for poly(A) polymerase I (PAP I). However, although importance of RNA polyadenylation has been demonstrated and biochemical properties of PAP I have been studied extensively, little is known about regulation of the pcnB gene transcription. Here, we demonstrate that there are three transcription start sites upstream of the pcnB coding sequence. Activities of at least two of these promoters were in inverse correlation to bacterial growth rates, which agrees with recently published results indicating increased abundance of PAP I and higher levels of RNA polyadenylation in slowly growing bacteria.

摘要

大约20年前,大肠杆菌的pcnB基因作为ColE1质粒拷贝数的调节因子被发现。进一步研究表明,该基因编码聚腺苷酸聚合酶I(PAP I)。然而,尽管RNA聚腺苷酸化的重要性已得到证实,并且对PAP I的生化特性也进行了广泛研究,但关于pcnB基因转录的调控却知之甚少。在此,我们证明在pcnB编码序列上游存在三个转录起始位点。其中至少两个启动子的活性与细菌生长速率呈负相关,这与最近发表的结果一致,即表明在生长缓慢的细菌中PAP I丰度增加且RNA聚腺苷酸化水平更高。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验