Letter | Published:

An allosteric mechanism of Rho-dependent transcription termination

Nature volume 463, pages 245249 (14 January 2010) | Download Citation

  • A Corrigendum to this article was published on 19 August 2010

Abstract

Rho is the essential RNA helicase that sets the borders between transcription units and adjusts transcriptional yield to translational needs in bacteria1,2,3. Although Rho was the first termination factor to be discovered4, the actual mechanism by which it reaches and disrupts the elongation complex (EC) is unknown. Here we show that the termination-committed Rho molecule associates with RNA polymerase (RNAP) throughout the transcription cycle; that is, it does not require the nascent transcript for initial binding. Moreover, the formation of the RNAP–Rho complex is crucial for termination. We show further that Rho-dependent termination is a two-step process that involves rapid EC inactivation (trap) and a relatively slow dissociation. Inactivation is the critical rate-limiting step that establishes the position of the termination site. The trap mechanism depends on the allosterically induced rearrangement of the RNAP catalytic centre by means of the evolutionarily conserved mobile trigger-loop domain, which is also required for EC dissociation. The key structural and functional similarities, which we found between Rho-dependent and intrinsic (Rho-independent) termination pathways, argue that the allosteric mechanism of termination is general and likely to be preserved for all cellular RNAPs throughout evolution.

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Acknowledgements

We thank I. Artsimovitch, S. Borukhov, K. Severinov, B. Stitt, D. Vassylyev and R. Weisberg for materials and discussions. This work was supported by a grant from the National Institutes of Health (R01GM58750, to E.N.).

Author Contributions V.E., D.D. and J.W. conducted the experimental work, discussed the results and commented on the manuscript. E.N. designed the study and wrote the paper.

Author information

Author notes

    • Vitaly Epshtein
    •  & Dipak Dutta

    These authors contributed equally to this work.

Affiliations

  1. Department of Biochemistry, New York University School of Medicine, New York, New York 10016, USA

    • Vitaly Epshtein
    • , Dipak Dutta
    •  & Evgeny Nudler
  2. Department of Biomedical Sciences, School of Public Health, University at Albany, Albany, New York 12201, USA

    • Joseph Wade

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Competing interests

The authors declare no competing financial interests.

Corresponding author

Correspondence to Evgeny Nudler.

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    Supplementary Information

    This file contains Supplementary Figures, 1-11 with Legends and Supplementary Notes and Supplementary Methods.

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https://doi.org/10.1038/nature08669

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