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      Panorama of ancient metazoan macromolecular complexes

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          Abstract

          Macromolecular complexes are essential to conserved biological processes, but their prevalence across animals is unclear. By combining extensive biochemical fractionation with quantitative mass spectrometry, we directly examined the composition of soluble multiprotein complexes among diverse metazoan models. Using an integrative approach, we then generated a draft conservation map consisting of >1 million putative high-confidence co-complex interactions for species with fully sequenced genomes that encompasses functional modules present broadly across all extant animals. Clustering revealed a spectrum of conservation, ranging from ancient Eukaryal assemblies likely serving cellular housekeeping roles for at least 1 billion years, ancestral complexes that have accrued contemporary components, and rarer metazoan innovations linked to multicellularity. We validated these projections by independent co-fractionation experiments in evolutionarily distant species, by affinity-purification and by functional analyses. The comprehensiveness, centrality and modularity of these reconstructed interactomes reflect their fundamental mechanistic significance and adaptive value to animal cell systems.

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          Most cited references30

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          A map of the interactome network of the metazoan C. elegans.

          To initiate studies on how protein-protein interaction (or "interactome") networks relate to multicellular functions, we have mapped a large fraction of the Caenorhabditis elegans interactome network. Starting with a subset of metazoan-specific proteins, more than 4000 interactions were identified from high-throughput, yeast two-hybrid (HT=Y2H) screens. Independent coaffinity purification assays experimentally validated the overall quality of this Y2H data set. Together with already described Y2H interactions and interologs predicted in silico, the current version of the Worm Interactome (WI5) map contains approximately 5500 interactions. Topological and biological features of this interactome network, as well as its integration with phenome and transcriptome data sets, lead to numerous biological hypotheses.
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            Is Open Access

            CORUM: the comprehensive resource of mammalian protein complexes—2009

            CORUM is a database that provides a manually curated repository of experimentally characterized protein complexes from mammalian organisms, mainly human (64%), mouse (16%) and rat (12%). Protein complexes are key molecular entities that integrate multiple gene products to perform cellular functions. The new CORUM 2.0 release encompasses 2837 protein complexes offering the largest and most comprehensive publicly available dataset of mammalian protein complexes. The CORUM dataset is built from 3198 different genes, representing ∼16% of the protein coding genes in humans. Each protein complex is described by a protein complex name, subunit composition, function as well as the literature reference that characterizes the respective protein complex. Recent developments include mapping of functional annotation to Gene Ontology terms as well as cross-references to Entrez Gene identifiers. In addition, a ‘Phylogenetic Conservation’ analysis tool was implemented that analyses the potential occurrence of orthologous protein complex subunits in mammals and other selected groups of organisms. This allows one to predict the occurrence of protein complexes in different phylogenetic groups. CORUM is freely accessible at (http://mips.helmholtz-muenchen.de/genre/proj/corum/index.html).
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              Comparative genomics of the eukaryotes.

              A comparative analysis of the genomes of Drosophila melanogaster, Caenorhabditis elegans, and Saccharomyces cerevisiae-and the proteins they are predicted to encode-was undertaken in the context of cellular, developmental, and evolutionary processes. The nonredundant protein sets of flies and worms are similar in size and are only twice that of yeast, but different gene families are expanded in each genome, and the multidomain proteins and signaling pathways of the fly and worm are far more complex than those of yeast. The fly has orthologs to 177 of the 289 human disease genes examined and provides the foundation for rapid analysis of some of the basic processes involved in human disease.
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                Author and article information

                Journal
                0410462
                6011
                Nature
                Nature
                Nature
                0028-0836
                1476-4687
                12 July 2016
                07 September 2015
                17 September 2015
                26 September 2016
                : 525
                : 7569
                : 339-344
                Affiliations
                [1 ]Donnelly Centre for Cellular and Biomolecular Research, University of Toronto, Toronto, Ontario, Canada
                [2 ]Center for Systems and Synthetic Biology, Institute for Cellular and Molecular Biology, University of Texas at Austin, Austin, Texas, USA
                [3 ]Department of Medical Biophysics, Toronto, Ontario, Canada
                [4 ]Department of Molecular Genetics, University of Toronto, Toronto, Ontario, Canada
                [5 ]Hospital for Sick Children, Toronto, Ontario, Canada
                [6 ]Department of Molecular Biosciences, University of Texas at Austin, Austin, Texas, USA
                [7 ]University of Regina, Regina, Saskatchewan, Canada
                [8 ]Max Planck Institute of Molecular Cell Biology and Genetics, Dresden, Germany
                Author notes
                [* ]Communicating authors – contact information: [AE] – CCBR Rm 914, 160 College Street, Toronto, Ontario, Canada M5S 3E1 Phone: 617-610-4042; Fax: 416-978-8528; andrew.emili@ 123456utoronto.ca . [EMM] – MBB 3.148, 2500 Speedway, Austin, Texas, USA 78712 Phone: 512-471-5435; Fax: 512-232-3472; marcotte@ 123456icmb.utexas.edu
                [#]

                These authors contributed equally to this work

                Correspondence and requests for materials should be addressed to E.M.M ( marcotte@ 123456icmb.utexas.edu ) or A.E. ( andrew.emili@ 123456utoronto.ca ).

                Article
                NIHMS704400
                10.1038/nature14877
                5036527
                26344197
                8e7fb277-d758-4616-8427-9a8d2a3842e3

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