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Predicting DNA hybridization kinetics from sequence

Abstract

Hybridization is a key molecular process in biology and biotechnology, but so far there is no predictive model for accurately determining hybridization rate constants based on sequence information. Here, we report a weighted neighbour voting (WNV) prediction algorithm, in which the hybridization rate constant of an unknown sequence is predicted based on similarity reactions with known rate constants. To construct this algorithm we first performed 210 fluorescence kinetics experiments to observe the hybridization kinetics of 100 different DNA target and probe pairs (36 nt sub-sequences of the CYCS and VEGF genes) at temperatures ranging from 28 to 55 °C. Automated feature selection and weighting optimization resulted in a final six-feature WNV model, which can predict hybridization rate constants of new sequences to within a factor of 3 with 91% accuracy, based on leave-one-out cross-validation. Accurate prediction of hybridization kinetics allows the design of efficient probe sequences for genomics research.

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Figure 1: Experimental characterization of hybridization kinetics.
Figure 2: Hybridization model and rate constant parameterization.
Figure 3: Summary of observed hybridization kinetics.
Figure 4: Rate constant prediction using the WNV model.
Figure 5: Prediction accuracy of the WNV model using different numbers of features.
Figure 6: Comparison of probes predicted to possess median versus fast hybridization kinetics for enrichment from human genomic DNA.

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References

  1. Hamilton, A. J. & Baulcombe, D. C. A species of small antisense RNA in posttranscriptional gene silencing in plants. Science 286, 950–952 (1999).

    Article  CAS  Google Scholar 

  2. Kornberg, A. & Baker, T. A. DNA Replication (Freeman, 1992).

    Google Scholar 

  3. Lewis, B. P., Burge, C. B. & Bartel, D. P. Conserved seed pairing, often flanked by adenosines, indicates that thousands of human genes are microRNA targets. Cell 120, 15–20 (2005).

    Article  CAS  Google Scholar 

  4. Izkoviz, S. & van Oudenaarden, A. Validating transcripts wih probes and imaging technology. Nat. Methods 8, S12–S19 (2011).

    Article  Google Scholar 

  5. Lockhart, D. J. et al. Expression monioring by hybridization to high-densiy oligonucleotide arrays. Nat. Biotechnol. 14, 1675–1680 (1996).

    Article  CAS  Google Scholar 

  6. Gnirke, A. et al. Solution hybrid selection wih ultra-long oligonucleotides for massively parallel targeted sequencing. Nat. Biotechnol. 27, 182–189 (2009).

    Article  CAS  Google Scholar 

  7. Khodakov, D., Wang, C. & Zhang, D. Y. Diagnostics based on nucleic acid sequence variant profiling: PCR, hybridization, and NGS approaches. Adv. Drug Delivery Rev. 105, 3–19 (2016).

    Article  CAS  Google Scholar 

  8. Mathews, D. H., Sabina, J., Zuker, M. & Turner, D. H. Expanded sequence dependence of thermodynamic parameters improves prediction of RNA secondary structure. J. Mol. Biol. 288, 911–940 (1999).

    Article  CAS  Google Scholar 

  9. SantaLucia, J. & Hicks, D. The thermodynamics of DNA structural motifs. Ann. Rev. Biochem. 33, 415–440 (2004).

    CAS  Google Scholar 

  10. Zuker, M. Mfold web server for nucleic acid folding and hybridization prediction. Nucleic Acids Res. 31, 3406–3415 (2003).

    Article  CAS  Google Scholar 

  11. Zadeh, J. N. et al. NUPACK: analysis and design of nucleic acid systems. J. Comput. Chem. 32, 170–173 (2011).

    Article  CAS  Google Scholar 

  12. Morrison, L. E. & Stols, L. M. Sensitive fluorescence-based thermodynamic and kinetic measurements of DNA hybridization in solution. Biochemistry 32, 3095–3104 (1993).

    Article  CAS  Google Scholar 

  13. Reynaldo, L. P., Vologodskii, A. V., Neri, B. P. & Lyamichev, V. I. The kinetics of oligonucleotide replacements. J. Mol. Biol. 297, 511–520 (2000).

    Article  CAS  Google Scholar 

  14. Zhang, D. Y. & Winfree, E. Control of DNA strand displacement kinetics using toehold exchange. J. Am. Chem. Soc. 131, 17303–17314 (2009).

    Article  CAS  Google Scholar 

  15. Ouldridge, T. E., Šulc, P., Romano, F., Doye, J. P. K. & Louis, A. A. DNA hybridization kinetics: zippering, internal displacement and sequence dependence. Nucleic Acids Res. 41, 8886–8895 (2013).

    Article  CAS  Google Scholar 

  16. Schreck, J. S. et al. DNA hairpins destabilize duplexes primarily by promoting melting rather than by inhibiting hybridization. Nucleic Acids Res. 43, 6181–6190 (2015).

    Article  CAS  Google Scholar 

  17. Cisse, I. I., Kim, H. & Ha, T. A rule of seven in Watson–Crick base-pairing of mismatched sequences. Nat. Struct. Mol. Biol. 19, 623–627 (2012).

    Article  CAS  Google Scholar 

  18. Jungmann, R. et al. Single-molecule kinetics and super-resolution microscopy by fluorescence imaging of transient binding on DNA origami. Nano Lett. 10, 4756–4761 (2010).

    Article  CAS  Google Scholar 

  19. He, G., Li, J., Ci, H., Qi, C. & Guo, X. Direct measurement of single-molecule DNA hybridization dynamics with single-base resolution. Angew. Chem. Int. Ed. 55, 9036–9040 (2016).

    Article  CAS  Google Scholar 

  20. Wang, J. S. & Zhang, D. Y. Simulation-guided DNA probe design for consistently ultraspecific hybridization. Nat. Chem. 7, 545–553 (2015).

    Article  CAS  Google Scholar 

  21. Gao, Y., Wolf, L. K. & Georgiadis, R. M. Secondary structure effects on DNA hybridization kinetics: a solution versus surface comparison. Nucleic Acids Res. 34, 3370–3377 (2006).

    Article  CAS  Google Scholar 

  22. van Dijk, E. L., Auger, H., Jaszczyszyn, Y. & Thermes, C. Ten years of next-generation sequencing technology. Trends Genet. 30, 418–426 (2014).

    Article  CAS  Google Scholar 

  23. Koboldt, D. C., Steinberg, K. M., Larson, D. E., Wilson, R. K. & Mardis, E. R. The next-generation sequencing revolution and is impact on genomics. Cell 155, 27–38 (2013).

    Article  CAS  Google Scholar 

  24. Chilamakuri, C. S. et al. Performance comparison of four exome capture systems for deep sequencing. BMC Genomics 15, 449 (2014).

    Article  Google Scholar 

  25. Clark, M. J. et al. Performance comparison of exome DNA sequencing technologies. Nat. Biotechnol. 29, 908–914 (2011).

    Article  CAS  Google Scholar 

  26. Snyder, M. W., Kircher, M., Hill, A. J., Daza, R. M. & Shendure, J. Cell-free DNA comprises an in vivo nucleosome footprint that informs is tissues-of-origin. Cell 164, 57–68 (2016).

    Article  CAS  Google Scholar 

  27. Denoeux, T. A k-nearest neighbor classification rule based on Dempster–Shafer theory. IEEE Trans. Syst. Man Cybern. 25, 804–813 (1995).

    Article  Google Scholar 

  28. Wand, M. P. & Jones, M. C. Kernel Smoothing (CRC Press, 1994).

    Book  Google Scholar 

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Acknowledgements

The authors thank S.X. Chen for assistance with NGS sequence alignment. This work was funded by National Institutes of Health grant R01HG008752 to D.Y.Z.

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Authors and Affiliations

Authors

Contributions

J.X.Z., L.R.W. and D.Y.Z. conceived the project. J.X.Z. and A.W.Z. performed the experiments. N.D. and A.P. performed hybridization reaction model fitting and selection. J.X.Z., J.Z.F., B.Y. and R.P. performed feature construction. W.D. and D.Y.Z. performed WNV model construction and optimization. N.D., B.Y. and R.P. performed MLR model construction and optimization. D.Y.Z. wrote the manuscript with input from all authors.

Corresponding author

Correspondence to David Yu Zhang.

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Competing interests

There is a patent pending on the X-probes used in this work, and a patent pending on the WNV model of hybridization rate constant prediction.

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Zhang, J., Fang, J., Duan, W. et al. Predicting DNA hybridization kinetics from sequence. Nature Chem 10, 91–98 (2018). https://doi.org/10.1038/nchem.2877

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