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一种用于细胞内镁离子(Mg²⁺)的RNA传感器。

An RNA sensor for intracellular Mg(2+).

作者信息

Cromie Michael J, Shi Yixin, Latifi Tammy, Groisman Eduardo A

机构信息

Howard Hughes Medical Institute, Department of Molecular Microbiology, Washington University School of Medicine, 660 South Euclid Avenue, Campus Box 8230, St. Louis, MO 63110, USA.

出版信息

Cell. 2006 Apr 7;125(1):71-84. doi: 10.1016/j.cell.2006.01.043.

Abstract

Most RNA molecules require Mg(2+) for their structure and enzymatic properties. Here we report the first example of an RNA serving as sensor for cytoplasmic Mg(2+). We establish that expression of the Mg(2+) transporter MgtA of Salmonella enterica serovar Typhimurium is controlled by its 5' untranslated region (5'UTR). We show that the 5'UTR of the mgtA gene can adopt different stem-loop structures depending on the Mg(2+) levels, which determine whether transcription reads through into the mgtA coding region or stops within the 5'UTR. We could recapitulate the Mg(2+)-regulated transcription using a defined in vitro transcription system with RNA polymerase as the only protein component. The initiation of mgtA transcription responds to extracytoplasmic Mg(2+) and its elongation into the coding region to cytoplasmic Mg(2+), providing a singular example in which the same ligand is sensed in different cellular compartments to regulate disparate steps in gene transcription.

摘要

大多数RNA分子的结构和酶活性都需要Mg(2+)。在此,我们报道了首个作为细胞质Mg(2+)传感器的RNA实例。我们证实,鼠伤寒沙门氏菌血清型鼠伤寒亚种的Mg(2+)转运蛋白MgtA的表达受其5'非翻译区(5'UTR)控制。我们表明,mgtA基因的5'UTR可根据Mg(2+)水平形成不同的茎环结构,这决定了转录是通读进入mgtA编码区还是在5'UTR内终止。我们能够使用以RNA聚合酶作为唯一蛋白质成分的特定体外转录系统重现Mg(2+)调控的转录过程。mgtA转录的起始对胞外Mg(2+)作出反应,其延伸进入编码区则对细胞质Mg(2+)作出反应,提供了一个独特的例子,即同一配体在不同细胞区室中被感知以调控基因转录的不同步骤。

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