The coordination between RNA polymerase and ribosome in bacteria

Our new paper published in Nature Microbiology provides new insight into the transcription-translation coordination in bacterial cells.
Published in Microbiology
The coordination between RNA polymerase and ribosome in bacteria

Share this post

Choose a social network to share with, or copy the shortened URL to share elsewhere

This is a representation of how your post may appear on social media. The actual post will vary between social networks

During the last year of my graduate stage in 2016 at Peking University, I had been struggling to publish my first Nature Microbiology paper (a giant paper with a 60-pages supplementary file) [1]. In that work, we investigated the quantitative principle of the coordination between growth rate and the protein translational capacity of E. coli under a broad range of growth conditions. Although mRNA transcription was not involved in that study, I began to think about the issue of transcription-translation coupling, a seemingly well-established notion for the gene expression process of prokaryotic cells. The coordination between transcription and translation had already been visualized half a century ago under electron microscopy: a trailing ribosome closely follows the elongating RNA polymerase (RNAP) during gene expression. The speed of ribosome and RNAP matches well with each other under various growth conditions. A leading model to account for this phenomenon is the ribosome-pushing-RNAP model: the trailing ribosome could effectively push the elongating RNAP by inhibiting the spontaneous backtracking of the latter, thereby matching the speed of RNAP with ribosome in many growth conditions [2]. In another word, the maintenance of RNAP elongating speed requires the assistance of ribosome. A series of recent biochemical and structural biology studies have further shown that the trailing ribosome has direct or indirect interaction with RNAP [3-7], providing evidences of a physical mechanism of the ribosome-RNAP coupling.

 At that time, I felt a bit not that convinced of the ribosome-pushing-RNAP model due to two reasons. First, Proshkin et al [2] used a sublethal dose of chloramphenicol to slow translational elongation speed and observed similar drop of transcriptional elongation speed. However, in my first Nature Microbiology paper [1], we found that various ribosome-targeting drugs including chloramphenicol did not cause slow-down of ribosome elongation, and instead, they function through reducing the fraction of actively translating ribosomes (we tried a lot of growth conditions and obtained the same conclusion). Second, the RNA polymerase can transcribe the non-translating ribosomal RNA (rRNA) at a very high speed, 90-100 nt/s, being much faster than the mRNA transcriptional speed (30-50 nt/s) [8]. This evidence suggests that the RNAP has a very high intrinsic moving speed. Then it seems counter-intuitive that RNAP requires ribosome to maintain its speed during transcribing mRNA. In March 2017, my wife (Dr. Manlu Zhu, the first author of this paper) and I obtained the faculty positions and established our own lab at Central China Normal University (CCNU). We skipped the postdoc stage, which we think was a big gambling at that time (we had a very hard time to find a suitable PI position due to the lack of postdoc experience). But we had a long to-do list including many interesting projects in mind and could not wait to play by ourselves. We began to investigate the issue of transcription-translation coordination shortly after we moved from Beijing to Wuhan, China. Professor Terry Hwa, who was our supervisor during our 2-years visit at UCSD (We did the work of Dai et al 2016 Nature Microbiology at Hwa Lab [1] from 2013 to 2015), had also been invited to participate into this project.

A technical challenge is to find a way to quantify the transcriptional kinetics of E. coli. Traditional radioactive dot-blotting assay (a northern blotting approach) is complicated, hazardous and has low resolution. The single-cell fluorescence in situ hybridization (FISH) is cool but requires single-cell microscopy platform, and the fluorescence probe is very expensive for a new established lab. We then tried qRT-PCR and it did work quite well. We confirmed the fact that transcriptional and translational elongation speed did match well with each other under various nutrient-limited conditions. The first key experiment in this project is to study the effect of fusidic acid on transcriptional elongation speed. Unlike chloramphenicol, fusidic acid is known to cause substantial slow-down of ribosome elongation speed. The result was awesome: the transcriptional elongation speed of E. coli was maintained during fusidic acid treatment, suggesting the occurrence of transcription-translation dissociation. This result strongly supports that ribosome is not required to maintain the speed of RNAP. This conclusion was further reinforced by the fact that transcriptional elongation speed is also maintained during nonsense mutation where translation is completely absent. The second important point is that we were able to quantitatively capture substantial Rho-mediated transcriptional premature termination (PTT) in cases where transcription-translation coordination is disrupted (e.g. antibiotics treatment and nonsense mutation). The PTT effect could be related to the reduction of active ribosome fraction during antibiotic treatment (a major point of Dai et al 2016 Nature Microbiology [1]). The last important point is that we found (p)ppGpp is involved in maintaining the transcriptional-translational coordination under various nutrient-limited conditions.

 It should be noted that currently we are still lack of a full picture of transcriptional-translational coordination of bacterial cells under other kinds of stress (e.g. low/high temperature, low pH, high osmolarity and oxidative stress). A combination of high throughout approaches, including ribosome profiling, RNA-seq and proteomic mass spec will help to elucidate the transcriptional-translation coordination status at the genome-scale. Lastly, it will be important to study the applicability and mechanism of transcriptional-translational coordination in other bacterial species that have large evolutionary distances from the model organism, Escherichia coli.


Link of the paper published in Nature Microbiology:


1.     Dai, X. et al. Reduction of translating ribosomes enables Escherichia coli to maintain elongation rates during slow growth. Nat Microbiol 2, 16231 (2016).

2.     Proshkin, S., Rahmouni, A. R., Mironov, A. & Nudler, E. Cooperation between translating ribosomes and RNA polymerase in transcription elongation. Science 328, 504-508, (2010).

3.     Kohler, R., Mooney, R. A., Mills, D. J., Landick, R. & Cramer, P. Architecture of a transcribing-translating expressome. Science 356, 194-197, (2017).

4.     Demo, G. et al. Structure of RNA polymerase bound to ribosomal 30S subunit. Elife 6, doi:10.7554/eLife.28560 (2017).

5.     Fan, H. et al. Transcription-translation coupling: direct interactions of RNA polymerase with ribosomes and ribosomal subunits. Nucleic Acids Res 45, 11043-11055, (2017).

6.     Burmann, B. M. et al. A NusE:NusG complex links transcription and translation. Science 328, 501-504, (2010).

7.     Burmann, B. M. et al. An alpha helix to beta barrel domain switch transforms the transcription factor RfaH into a translation factor. Cell 150, 291-303, doi:10.1016/j.cell.2012.05.042 (2012).

8.     Klumpp, S. and Hwa, T. (2008) Stochasticity and traffic jams in the transcription of ribosomal RNA: Intriguing role of termination and antitermination. Proc Natl Acad Sci U S A, 105, 18159-18164.




Please sign in or register for FREE

If you are a registered user on Research Communities by Springer Nature, please sign in