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An empirical framework for binary interactome mapping

Abstract

Several attempts have been made to systematically map protein-protein interaction, or 'interactome', networks. However, it remains difficult to assess the quality and coverage of existing data sets. Here we describe a framework that uses an empirically-based approach to rigorously dissect quality parameters of currently available human interactome maps. Our results indicate that high-throughput yeast two-hybrid (HT-Y2H) interactions for human proteins are more precise than literature-curated interactions supported by a single publication, suggesting that HT-Y2H is suitable to map a significant portion of the human interactome. We estimate that the human interactome contains 130,000 binary interactions, most of which remain to be mapped. Similar to estimates of DNA sequence data quality and genome size early in the Human Genome Project, estimates of protein interaction data quality and interactome size are crucial to establish the magnitude of the task of comprehensive human interactome mapping and to elucidate a path toward this goal.

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Figure 1: Conceptual framework for interactome mapping.
Figure 2: Assay sensitivity and background positive rate of binary interactome mapping assays.
Figure 3: Precision and sampling sensitivity in interactome data sets.
Figure 4: Analysis of interacting pairs in CCSB-HI1 and MDC-HI1 interactome maps for their ability to share specific Gene Ontology (GO) functional annotations.

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Acknowledgements

We thank members of CCSB and the Vidal, Barabasi, Wanker and Tavernier laboratories and S. Sahasrabuddhe, R. Bell, R. Chettier and C. Wiggins for helpful discussions; E. Smith for help generating Figure 1; and Agencourt Biosciences for sequencing assistance. This work was supported by the US National Human Genome Research Institute (2R01HG001715 and 5P50HG004233 to M.V. and F.P.R.), the US National Cancer Institute (5U54CA112952 to J. Nevins, subcontract to M.V.; and 5U01CA105423 to S.H. Orkin, project to M.V.), the US National Institutes of Health (IH U01 A1070499-01 and U56 CA113004 to A.-L.B. and postdoctoral training grant fellowship T32CA09361 to K.V.), the Ellison Foundation (to M.V.), the W.M. Keck Foundation (to M.V.), Dana-Farber Cancer Institute Institute Sponsored Research funds (to M.V.), the US National Science Foundation (ITR DMR-0926737 and IIS-0513650 to A.-L.B.), Deutsches Bundesministerium für Bildung und Forschung (NGFN2, KB-P04T01, KB-P04T03 and 01GR0471 to E.E.W. and U.S.), Deutsche Forschungsgemeinschaft (SFB 577 and SFB618 to E.E.W.), the University of Ghent and the “Fonds Wetenschappelijk Onderzoek–Vlaanderen” (FWO-V) G.0031.06 (GOA12051401 to J. Tavernier) and the National Cancer Institute of Canada (to C.B.). I.L. is a postdoctoral fellow with the FWO-V. M.V. is a “Chercheur Qualifié Honoraire” from the Fonds de la Recherche Scientifique (French Community of Belgium).

Author information

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Authors

Contributions

K.V., J.-F.R., A. Vazquez, U.S., I.L., J. Tavernier, E.E.W., A.-L.B. and M.V. conceived the project. K.V., J.-F.R., A. Vazquez, U.S. and I.L. coordinated the experiments and data analyses. J.-F.R., U.S., T.H.-K., M.Z., X.X., K.H., F.G., J.M.S., P.B., H.Y., S.C., C.S., E.D., J. Timm, K.R. and C.B. conducted the Y2H experiments. J.-F.R., T.H.-K. and C.S. conducted the high-throughput ORF cloning for MAPPIT experiments. I.L. and A.-S.d.S. conducted the MAPPIT experiments. K.V., A. Vazquez, T.H., K.-I.G., M.A.Y., A. Vinayagam, N.S., N.K., C.L., M.L. and F.P.R. conducted the computational and statistical analyses. M.E.C., A.S., H.B., J.-F.R. and K.V. conducted the literature-curated interaction recuration analyses. D.S., A.D. and R.R.M. provided laboratory support. K.V., J.-F.R., A. Vazquez, U.S., I.L., M.E.C., D.E.H., J. Tavernier, E.E.W., A.-L.B. and M.V. wrote the manuscript. D.E.H, J. Tavernier, E.E.W., A.-L.B. and M.V. codirected the project.

Corresponding authors

Correspondence to Jan Tavernier, Erich E Wanker, Albert-László Barabási or Marc Vidal.

Supplementary information

Supplementary Text and Figures

Supplementary Figure 1; Supplementary Tables 2,3,5; Supplementary Data 1–4; Supplementary Methods (PDF 2639 kb)

Supplementary Table 1

List of interactions in various datasets used in pair wise test experiments using MAPPIT and Y2H-CCSB assays (XLS 144 kb)

Supplementary Table 4

Scores for the Y2H-CCSB and MAPPIT experiments on the hsPRS-v1 and hsRRS-v1 to compute assay sensitivity and background positive rate and scores on subsets of the LC, MDC-HI1 and CCSB-HI1 interaction datasets (XLS 78 kb)

Supplementary Table 6

Identity of the ORFs making up the Y2H-CCSB repeat screens (XLS 396 kb)

Supplementary Table 7

Interactions found in the Y2H-CCSB repeat screens (XLS 69 kb)

Supplementary Table 8

Interactions found in the Y2H-CCSB repeat screens reported according to MIMIX specifications (XLS 207 kb)

Supplementary Table 9

Identity of the ORFs making up the MDC-HI1 search space (space II) (XLS 159 kb)

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Venkatesan, K., Rual, JF., Vazquez, A. et al. An empirical framework for binary interactome mapping. Nat Methods 6, 83–90 (2009). https://doi.org/10.1038/nmeth.1280

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