RNA polymerases display collaborative and antagonistic group behaviors over long distances through DNA supercoiling

Author:

Kim SangjinORCID,Beltran Bruno,Irnov Irnov,Jacobs-Wagner ChristineORCID

Abstract

SUMMARYTranscription by RNA polymerases (RNAPs) is essential for cellular life. Genes are often transcribed by multiple RNAPs. While the properties of individual RNAPs are well appreciated, it remains less explored whether group behaviors can emerge from co-transcribing RNAPs under most physiological levels of gene expression. Here, we provide evidence inEscherichia colithat well-separated RNAPs can exhibit collaborative and antagonistic group dynamics. Co-transcribing RNAPs translocate faster than a single RNAP, but the density of RNAPs has no significant effect on their average speed. When a promoter is inactivated, RNAPs that are far downstream from the promoter slow down and experience premature dissociation, but only in the presence of other co-transcribing RNAPs. These group behaviors depend on transcription-induced DNA supercoiling, which can also mediate inhibitory dynamics between RNAPs from neighboring divergent genes. Our findings suggest that transcription on topologically-constrained DNA, a norm across organisms, can provide an intrinsic mechanism for modulating the speed and processivity of RNAPs over long distances according to the promoter’s on/off state.

Publisher

Cold Spring Harbor Laboratory

Reference73 articles.

1. The Synthesis and Degradation of Lactose Operon Messenger RNA in E. coli

2. Bachmann, B.J. (1996). Derivations and genotypes of some mutant derivatives of Escherichia coli K-12, Vol 2, 2nd edn (Washington, DC: ASM Press).

3. Many expressed genes in bacteria and yeast are transcribed only once per cell cycle

4. High throughput real time quantitative reverse transcription PCR;Curr. Protoc. Mol. Biol.,2006

5. Energetics at the DNA Supercoiling Transition

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