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一种RNA解旋酶细菌转录终止子的DNA结合

DNA binding of an RNA helicase bacterial transcription terminator.

作者信息

Jain Sriyans, Behera Abhijeet, Sen Ranjan

机构信息

Laboratory of Transcription, Centre for DNA Fingerprinting and Diagnostics, Inner Ring Road, Uppal, Hyderabad, 500039, India.

Centre for Doctoral Studies, Manipal Academy of Higher Education, Manipal, Karnataka, India.

出版信息

Biochem J. 2025 Feb 5;482(3):103-117. doi: 10.1042/BCJ20240452.

Abstract

The bacterial transcription terminator Rho is a hexameric ATP-dependent RNA helicase that dislodges elongating RNA polymerases. It has an N-terminal primary RNA binding site (PBS) on each subunit and a C-terminal secondary RNA binding site at the central channel. Here, we show that Rho also binds to linear longer double-stranded DNAs (dsDNAs) and the circular plasmids nonspecifically using its PBS. However, this interaction could be competed efficiently by single-stranded DNA (ssDNA), dC34. Long dsDNA (3.5 kb) at the PBS activates short oligo C RNA-mediated ATPase activity at the secondary binding site (SBS). The pre-bound Rho to this long DNA reduces the rate and efficiency of its transcription termination activities in vitro. Elevated concentrations of Rho reduced the in vitro transcription level suggesting that Rho might also function as a nonspecific repressor of gene expression under certain conditions. In the mid-log phase culture, Rho molecules were concentrated at the poles and along the membrane. In contrast, the Rho hexamers were observed to be distributed over the bacterial chromosome in the stationary phase likely in a hyper-oligomeric state composed of oligomers of hexamers. We propose that Rho molecules not engaged in the transcription termination process could use the bacterial chromosome as a "resting surface". This way the "idle" DNA-bound Rho molecules could be kept away from accidentally loading onto the nascent RNA and initiating unwanted transcription termination.

摘要

细菌转录终止因子Rho是一种六聚体ATP依赖性RNA解旋酶,可使延伸的RNA聚合酶脱离。它在每个亚基上有一个N端初级RNA结合位点(PBS),在中央通道有一个C端次级RNA结合位点。在这里,我们表明Rho还利用其PBS非特异性地结合线性较长的双链DNA(dsDNA)和环状质粒。然而,这种相互作用可以被单链DNA(ssDNA)dC34有效竞争。PBS处的长dsDNA(3.5 kb)激活次级结合位点(SBS)处短寡聚C RNA介导的ATPase活性。预先结合到这种长DNA上的Rho降低了其体外转录终止活性的速率和效率。Rho浓度升高降低了体外转录水平,这表明在某些条件下,Rho也可能作为基因表达的非特异性阻遏物发挥作用。在对数中期培养中,Rho分子集中在两极并沿细胞膜分布。相反,在稳定期观察到Rho六聚体分布在细菌染色体上,可能处于由六聚体寡聚体组成的超寡聚状态。我们提出,未参与转录终止过程的Rho分子可以将细菌染色体用作“静止表面”。通过这种方式,“闲置”的与DNA结合的Rho分子可以避免意外加载到新生RNA上并引发不必要的转录终止。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/76ee/12133298/ae3152874867/bcj-482-3-BCJ20240452-g001.jpg

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