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参与质粒R1复制调控的RepA mRNA前导转录本的二级结构分析。

Secondary structure analysis of the RepA mRNA leader transcript involved in control of replication of plasmid R1.

作者信息

Ohman M, Wagner E G

机构信息

Department of Microbiology, Uppsala University, Sweden.

出版信息

Nucleic Acids Res. 1989 Apr 11;17(7):2557-79. doi: 10.1093/nar/17.7.2557.

Abstract

The main replication control function in plasmid R1 is an antisense RNA, CopA RNA. By binding to its target (CopT) in the leader of the RepA mRNA, CopA RNA inhibits the expression of the rate-limiting RepA protein. The formation of the RNA duplex has been proposed to alter the folding around the RepA start region. Knowledge of the secondary structure of both CopA and CopT RNA is crucial for an understanding of the regulation. Previously, we reported the structure of CopA RNA under native conditions. In the present communication we have analyzed the secondary structure of the RepA leader transcript. Our main findings are: The two loops of CopA RNA have their correspondence in CopT RNA. No major structural changes are found downstream of the duplex when CopA was bound to its target RNA during transcription. Furthermore, in agreement with CopA/CopT RNA binding studies reported recently we do not find evidence for the existence of a binding window.

摘要

质粒R1中的主要复制控制功能由一种反义RNA,即CopA RNA发挥。通过与RepA mRNA前导区的靶标(CopT)结合,CopA RNA抑制限速性RepA蛋白的表达。有人提出RNA双链体的形成会改变RepA起始区域周围的折叠。了解CopA和CopT RNA的二级结构对于理解这种调控至关重要。此前,我们报道了天然条件下CopA RNA的结构。在本通讯中,我们分析了RepA前导转录本的二级结构。我们的主要发现如下:CopA RNA的两个环在CopT RNA中有对应结构。转录过程中当CopA与其靶标RNA结合时,在双链体下游未发现重大结构变化。此外,与最近报道的CopA/CopT RNA结合研究一致,我们没有发现存在结合窗口的证据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c1e/317643/98eca4a6d1a0/nar00124-0193-a.jpg

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