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Systematic dissection and optimization of inducible enhancers in human cells using a massively parallel reporter assay

Nature Biotechnology volume 30, pages 271277 (2012) | Download Citation


Learning to read and write the transcriptional regulatory code is of central importance to progress in genetic analysis and engineering. Here we describe a massively parallel reporter assay (MPRA) that facilitates the systematic dissection of transcriptional regulatory elements. In MPRA, microarray-synthesized DNA regulatory elements and unique sequence tags are cloned into plasmids to generate a library of reporter constructs. These constructs are transfected into cells and tag expression is assayed by high-throughput sequencing. We apply MPRA to compare >27,000 variants of two inducible enhancers in human cells: a synthetic cAMP-regulated enhancer and the virus-inducible interferon-β enhancer. We first show that the resulting data define accurate maps of functional transcription factor binding sites in both enhancers at single-nucleotide resolution. We then use the data to train quantitative sequence-activity models (QSAMs) of the two enhancers. We show that QSAMs from two cellular states can be combined to design enhancer variants that optimize potentially conflicting objectives, such as maximizing induced activity while minimizing basal activity.

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The authors would like to thank E.M. LeProust and S. Chen of Agilent for oligonucleotide library synthesis, R.P. Deering for assistance with Sendai virus infections and the staff of the Broad Institute and the Bauer Core facilities for assistance with data generation. This project was supported by funds from the Broad Institute, the Harvard Stem Cell Institute (T.S.M.), National Human Genome Research Institute grant R01HG004037 (M.K.), the Simons Center for Quantitative Biology at Cold Spring Harbor Laboratory (J.B.K.), National Science Foundation (NSF) grant PHY-0957573 (C.G.C., T.T.) and NSF grant PHY-1022140 (A. Mur.).

Author information

Author notes

    • Alexandre Melnikov
    • , Anand Murugan
    •  & Xiaolan Zhang

    These authors contributed equally to this work.


  1. Broad Institute, Cambridge, Massachusetts, USA.

    • Alexandre Melnikov
    • , Xiaolan Zhang
    • , Li Wang
    • , Peter Rogov
    • , Soheil Feizi
    • , Andreas Gnirke
    • , Manolis Kellis
    • , Eric S Lander
    •  & Tarjei S Mikkelsen
  2. Department of Physics, Princeton University, Princeton, New Jersey, USA.

    • Anand Murugan
    • , Tiberiu Tesileanu
    •  & Curtis G Callan Jr
  3. Simons Center for Systems Biology, Institute for Advanced Study, Princeton, New Jersey, USA.

    • Tiberiu Tesileanu
    •  & Curtis G Callan Jr
  4. MIT Computer Science and Artificial Intelligence Laboratory, Cambridge, Massachusetts, USA.

    • Soheil Feizi
    •  & Manolis Kellis
  5. Simons Center for Quantitative Biology, Cold Spring Harbor Laboratory, Cold Spring Harbor, New York, USA.

    • Justin B Kinney
  6. Department of Biology, Massachusetts Institute of Technology, Cambridge, Massachusetts, USA.

    • Eric S Lander
  7. Department of Systems Biology, Harvard Medical School, Boston, Massachusetts, USA.

    • Eric S Lander
  8. Harvard Stem Cell Institute and Department of Stem Cell and Regenerative Biology, Harvard University, Cambridge, Massachusetts, USA.

    • Tarjei S Mikkelsen


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A. Mel., X.Z., P.R., A.G. and T.S.M. developed MPRA and performed the molecular biology experiments. L.W. cultured the cells, and performed the plasmid transfections and luciferase assays. A.Mur., T.T., S.F., C.G.C., J.B.K., M.K., E.S.L. and T.S.M. analyzed the data. T.S.M. wrote the main text with substantial input from all authors. C.G.C. and J.B.K. wrote the Supplementary Notes with substantial input from A. Mur. and T.S.M.

Competing interests

A patent application describing ideas presented in this article has been filed by the Broad Institute.

Corresponding author

Correspondence to Tarjei S Mikkelsen.

Supplementary information

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  1. 1.

    Supplementary Text and Figures

    Supplementary Tables 5,6, Supplementary Notes and Supplementary Figs. 1–10

Excel files

  1. 1.

    Supplementary Table 1

    CRE variants

  2. 2.

    Supplementary Table 2

    IFNB variants

  3. 3.

    Supplementary Table 3

    CRE mutagenesis/models

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    Supplementary Table 4

    IFNB mutagenesis/models

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