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Translocation step size and mechanism of the RecBC DNA helicase

Abstract

DNA helicases are ubiquitous enzymes that unwind double-stranded DNA1,2,3. They are a diverse group of proteins that move in a linear fashion along a one-dimensional polymer lattice—DNA—by using a mechanism that couples nucleoside triphosphate hydrolysis to both translocation and double-stranded DNA unwinding to produce separate strands of DNA. The RecBC enzyme is a processive DNA helicase that functions in homologous recombination in Escherichia coli; it unwinds up to 6,250 base pairs per binding event and hydrolyses slightly more than one ATP molecule per base pair unwound. Here we show, by using a series of gapped oligonucleotide substrates, that this enzyme translocates along only one strand of duplex DNA in the 3′ → 5′ direction. The translocating enzyme will traverse, or ‘step’ across, single-stranded DNA gaps in defined steps that are 23 (±2) nucleotides in length. This step is much larger than the amount of double-stranded DNA that can be unwound using the free energy derived from hydrolysis of one molecule of ATP, implying that translocation and DNA unwinding are separate events. We propose that the RecBC enzyme both translocates and unwinds by a quantized, two-step, inchworm-like mechanism that may have parallels for translocation by other linear motor proteins.

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Figure 1: The RecBC helicase translocates in the 3′ → 5′ direction.
Figure 2: The observed step size for the translocating RecBC enzyme is 23 (±2) nucleotides.
Figure 3: The observed step size is dependent on the length of the proximal duplex DNA region and displays a 23-nt periodicity for 3 cycles of translocation and DNA unwinding.
Figure 4: The RecBC enzyme translocates by a ‘quantum inchworm’ mechanism.

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References

  1. Matson, S. W., Bean, D. W. & George, J. W. DNA helicases: enzymes with essential roles in all aspects of DNA metabolism. Bioessays 16, 13–22 (1994).

    Article  CAS  Google Scholar 

  2. Lohman, T. M. & Bjornson, K. P. Mechanisms of helicase-catalyzed DNA unwinding. Annu. Rev. Biochem. 65, 169 –214 (1996).

    Article  CAS  Google Scholar 

  3. West, S. C. DNA helicases: new breeds of translocating motors and molecular pumps. Cell 86, 177–80 ( 1996).

    Article  CAS  Google Scholar 

  4. Ganesan, S. & Smith, G. R. Strand-specific binding to duplex DNA ends by the subunits of Escherichia coli recBCD enzyme. J. Mol. Biol. 229, 67–78 (1993).

    Article  CAS  Google Scholar 

  5. Korangy, F. & Julin, D. A. Kinetics and processivity of ATP hydrolysis and DNA unwinding by the RecBC enzyme from Escherichia coli . Biochemistry 32, 4873– 4880 (1993).

    Article  CAS  Google Scholar 

  6. Ali, J. A. & Lohman, T. M. Kinetic measurement of the step size of DNA unwinding by Escherichia coli UvrD helicase. Science 275, 377–380 (1997); erratum, ibid 276, 21 (1997).

    Article  Google Scholar 

  7. Roman, L. J. & Kowalczykowski, S. C. Characterization of the adenosinetriphosphatase activity of the Escherichia coli RecBCD enzyme: Relationship of ATP hydrolysis to the unwinding of duplex DNA. Biochemistry 28, 2873–2881 (1989).

    Article  CAS  Google Scholar 

  8. Korangy, F. & Julin, D. A. A mutation in the consensus ATP-binding sequence of the RecD subunit reduces the processivity of the RecBCD enzyme from Escherichia coli. J. Biol. Chem. 267, 3088–3095 (1992).

    CAS  PubMed  Google Scholar 

  9. Taylor, A. F. & Smith, G. R. Monomeric RecBCD enzyme binds and unwinds DNA. J. Biol. Chem. 270, 24451– 24458 (1995).

    Article  CAS  Google Scholar 

  10. Bianco, P. R. & Kowalczykowski, S. C. The recombination hotspot Chi is recognized by the translocating RecBCD enzyme as the single strand of DNA containing the sequence 5′-GCTGGTGG-3′. Proc. Natl Acad. Sci. USA 94, 6706–6711 (1997).

    Article  ADS  CAS  Google Scholar 

  11. Chamberlin, M. J. New models for the mechanism of transcription elongation and its regulation. Harvey Lectures 88, 1– 21 (1992).

    PubMed  Google Scholar 

  12. Korangy, F. & Julin, D. A. Efficiency of ATP hydrolysis and DNA unwinding by the RecBC enzyme from Escherichia coli. Biochemistry 33, 9552–9560 (1994).

    Article  CAS  Google Scholar 

  13. Subramanya, H. S., Bird, L. E., Brannigan, J. A. & Wigley, D. B. Crystal structure of a DExx box DNA helicase. Nature 384, 379–383 (1996).

    Article  ADS  CAS  Google Scholar 

  14. Velankar, S. S., Soultanas, P., Dillingham, M. S., Subramanya, H. S. & Wigley, D. B. Crystal structures of complexes of PcrA DNA helicase with a DNA substrate indicate an inchworm mechanism. Cell 97, 75– 84 (1999).

    Article  CAS  Google Scholar 

  15. Korolev, S., Hsieh, J., Gauss, G. H., Lohman, T. M. & Waksman, G. Major domain swiveling revealed by the crystal structures of complexes of E. coli Rep helicase bound to single-stranded DNA and ADP. Cell 90, 635–647 (1997).

    Article  CAS  Google Scholar 

  16. Bird, L. E., Subramanya, H. S. & Wigley, D. B. Helicases: a unifying structural theme? Curr. Opin. Struct. Biol. 8, 14–18 (1998).

    Article  CAS  Google Scholar 

  17. Mechanic, L. E., Hall, M. C. & Matson, S. W. Escherichia coli DNA helicase II is active as a monomer. J. Biol. Chem. 274, 12488– 12498 (1999).

    Article  CAS  Google Scholar 

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Acknowledgements

We thank D. Anderson, R. Ando, D. Arnold, C. Barnes, R. Baskin, F. Chedin, F. Harmon, J. Kleiman, J. New, E. Seitz, and S. Shetterley for their comments. This work was supported by a grant from the NIH.

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Correspondence to Stephen C. Kowalczykowski.

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Bianco, P., Kowalczykowski, S. Translocation step size and mechanism of the RecBC DNA helicase. Nature 405, 368–372 (2000). https://doi.org/10.1038/35012652

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