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大肠杆菌中 GcvB 介导的 oppA mRNA 调控与二级假定 RNA-RNA 相互作用位点相关吗?

Is the secondary putative RNA-RNA interaction site relevant to GcvB mediated regulation of oppA mRNA in Escherichia coli?

机构信息

UPR CNRS n° 9073, Affiliated with Université Paris Diderot-Paris 7 Institut de Biologie Physico-Chimique, 13 rue Pierre et Marie Curie, 75005 Paris, France.

出版信息

Biochimie. 2010 Oct;92(10):1458-61. doi: 10.1016/j.biochi.2010.06.020. Epub 2010 Jul 24.

Abstract

GcvB is a non-coding RNA that regulates oppA mRNA in different bacterial species by binding a GcvB GU-rich region named R1 to oppA mRNA. A secondary putative interaction site (PS1) was identified in this study that is able to form a second nearly perfect 10 base-pair duplex between these two RNAs in Escherichia coli. In this work, we have studied whether the formation of a second interaction site could help stabilize the previously reported GcvB/oppA complex. Several mutations and the full deletion of PS1 were engineered. None of these modifications affected the ability of GcvB to control OppA expression. Therefore the second, putative, interaction site appears to be unnecessary for the regulatory function of GcvB with regard to its oppA target mRNA.

摘要

GcVB 是一种非编码 RNA,通过与 oppA mRNA 上名为 R1 的 GcVB GU 富含区域结合,在不同的细菌物种中调节 oppA mRNA。本研究鉴定了一个二级假定相互作用位点 (PS1),该位点能够在大肠杆菌中形成这两个 RNA 之间的第二个几乎完美的 10 碱基对双链。在这项工作中,我们研究了形成第二个相互作用位点是否有助于稳定之前报道的 GcVB/oppA 复合物。设计了几种突变和 PS1 的完全缺失。这些修饰都没有影响 GcVB 控制 OppA 表达的能力。因此,第二个假定的相互作用位点对于 GcVB 调节其 oppA 靶标 mRNA 的功能似乎是不必要的。

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