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Matrix and Steiner-triple-system smart pooling assays for high-performance transcription regulatory network mapping

Abstract

Yeast one-hybrid (Y1H) assays provide a gene-centered method for the identification of interactions between gene promoters and regulatory transcription factors (TFs). To date, Y1H assays have involved library screens that are relatively expensive and laborious. We present two Y1H strategies that allow immediate prey identification: matrix assays that use an array of 755 individual Caenorhabditis elegans TFs, and smart-pool assays that use TF multiplexing. Both strategies simplify the Y1H pipeline and reduce the cost of protein-DNA interaction identification. We used a Steiner triple system (STS) to create smart pools of 4–25 TFs. Notably, we uniplexed a small number of highly connected TFs to allow efficient assay deconvolution. Both strategies outperform library screens in terms of coverage, confidence and throughput. These versatile strategies can be adapted both to TFs in other systems and, likely, to other biomolecules and assays as well.

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Figure 1: Identified PDIs.
Figure 2: STS-based smart-pooling design.
Figure 3: Experimental validation of STS smart pools by Y1H assays using Pfat-5 as a DNA bait.
Figure 4: Comparison of different Y1H assays.

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References

  1. Walhout, A.J.M. Unraveling transcription regulatory networks by protein-DNA and protein-protein interaction mapping. Genome Res. 16, 1445–1454 (2006).

    Article  CAS  Google Scholar 

  2. Deplancke, B., Dupuy, D., Vidal, M. & Walhout, A.J.M.A. Gateway-compatible yeast one-hybrid system. Genome Res. 14, 2093–2101 (2004).

    Article  CAS  Google Scholar 

  3. Deplancke, B. et al. A gene-centered C. elegans protein-DNA interaction network. Cell 125, 1193–1205 (2006).

    Article  CAS  Google Scholar 

  4. Vermeirssen, V. et al. Transcription factor modularity in a gene-centered C. elegans core neuronal protein-DNA interaction network. Genome Res.; published online 18 May 2007.

  5. Walhout, A.J.M. et al. GATEWAY recombinational cloning: application to the cloning of large numbers of open reading frames or ORFeomes. Methods Enzymol. 328, 575–592 (2000).

    Article  CAS  Google Scholar 

  6. Colbourn, C. & Mathon, R. in The CRC Handbook of Combinatorial Designs. (eds. Colbourn, C. & Dinitz, J.) 66–75 (CRC Press, Boca Raton, Florida, USA, 1996).

    Book  Google Scholar 

  7. Reece-Hoyes, J.S. et al. A compendium of C. elegans regulatory transcription factors: a resource for mapping transcription regulatory networks. Genome Biol. 6, R110 (2005).

    Article  Google Scholar 

  8. Lamesch, P. et al. C. elegans ORFeome version 3.1: increasing the coverage of ORFeome resources with improved gene predictions. Genome Res. 14, 2064–2069 (2004).

    Article  CAS  Google Scholar 

  9. Wei, C. et al. Closing in on the C. elegans ORFeome by cloning TWINSCAN predictions. Genome Res. 15, 577–582 (2005).

    Article  CAS  Google Scholar 

  10. Hartley, J.L., Temple, G.F. & Brasch, M.A. DNA cloning using in vitro site-specific recombination. Genome Res. 10, 1788–1795 (2000).

    Article  CAS  Google Scholar 

  11. Walhout, A.J.M. et al. Protein interaction mapping in C. elegans using proteins involved in vulval development. Science 287, 116–122 (2000).

    Article  CAS  Google Scholar 

  12. Barrasa, M.I., Vaglio, P., Cavasino, F., Jacotot, L. & Walhout, A.J.M. EDGEdb: a transcription factor-DNA interaction database for the analysis of C. elegans differential gene expression. BMC Genomics 8, 21 (2007).

    Article  Google Scholar 

  13. Jin, F. et al. A pooling-deconvolution strategy for biological network elucidation. Nat. Methods 3, 183–189 (2006).

    Article  CAS  Google Scholar 

  14. Thierry-Mieg, N. A new pooling strategy for high-throughput screening: the Shifted Transversal Design. BMC Bioinformatics 7, 28 (2006).

    Article  Google Scholar 

  15. Thierry-Mieg, N. Pooling in systems biology becomes smart. Nat. Methods 3, 161–162 (2006).

    Article  CAS  Google Scholar 

  16. Li, S. et al. A map of the interactome network of the metazoan C elegans. Science 303, 540–543 (2004).

    Article  CAS  Google Scholar 

  17. Deplancke, B., Vermeirssen, V., Arda, H.E., Martinez, N.J. & Walhout, A.J.M. Gateway-compatible yeast one-hybrid screens. CSH Protocols (doi:10.1101/pdb.prot4590; 2006).

    Article  Google Scholar 

  18. Walhout, A.J.M. & Vidal, M. High-throughput yeast two-hybrid assays for large-scale protein interaction mapping. Methods 24, 297–306 (2001).

    Article  CAS  Google Scholar 

  19. Zhong, J., Zhang, H., Stanyon, C.A., Tromp, G. & Finley, R.L., Jr. A strategy for constructing large protein interaction maps using the yeast two-hybrid system: regulated expression arrays and two-phase mating. Genome Res. 13, 2691–2699 (2003).

    Article  CAS  Google Scholar 

  20. Reboul, J. et al. C. elegans ORFeome version 1.1: experimental verification of the genome annotation and resource for proteome-scale protein expression. Nat. Genet. 34, 35–41 (2003).

    Article  Google Scholar 

  21. Hillier, L. & Green, P. OSP: a computer program for choosing PCR and DNA sequencing primers. PCR Methods Appl. 1, 124–128 (1991).

    Article  CAS  Google Scholar 

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Acknowledgements

We thank J. Dekker for critical reading of the manuscript; W. Harper (Harvard Medical School) for the Y187 yeast strain; N. Klitgord and M. Vidal (Dana-Farber Cancer Institute) for help with primer design; E. Méndez González (M-3 Informática, S.L.) for helpful suggestions regarding constraint programming and the sequencing staff at Agencourt Bioscience Corporation for technical assistance. This work was supported by BAEF fellowship for Biomedical and Biotechnology Research to V.V., and US National Institute of Diabetes and Digestive and Kidney Diseases grants (DK068429 and DK071713) to A.J.M.W.

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Contributions

V.V., B.D., J.S.R.-H, H.E.A., C.A.G. and N.J.M. performed all experiments; B.D., M.I.B. and A.J.M.W. conceived the pooling strategy; M.I.B. created the STS design and deconvolution, and performed the bioinformatics analyses. M.R.B. provided TWINSCAN predictions. R.S. and L.D.-S. provided sequencing; V.V., J.S.R.-H. and A.J.M.W. wrote the manuscript.

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R.S. and L.D.-S. work for Agencourt bioscience.

Supplementary information

Supplementary Text and Figures

Supplementary Figures 1–4, Supplementary Tables 2–3, Supplementary Methods. (PDF 876 kb)

Supplementary Table 1

wTF2.1 and clone source and availability. (XLS 515 kb)

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Vermeirssen, V., Deplancke, B., Barrasa, M. et al. Matrix and Steiner-triple-system smart pooling assays for high-performance transcription regulatory network mapping. Nat Methods 4, 659–664 (2007). https://doi.org/10.1038/nmeth1063

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