A map of human protein interactions derived from co-expression of human mRNAs and their orthologs

被引:63
作者
Ramani, Arun K. [2 ]
Li, Zhihua [2 ]
Hart, G. Traver [2 ]
Carlson, Mark W. [3 ]
Boutz, Daniel R. [2 ]
Marcotte, Edward M. [1 ,2 ]
机构
[1] Univ Texas Austin, Dept Chem & Biochem, Austin, TX 78712 USA
[2] Univ Texas Austin, Inst Cellular & Mol Biol, Ctr Syst & Synthet Biol, Austin, TX 78712 USA
[3] Univ Texas Austin, Dept Biomed Engn, Austin, TX 78712 USA
关键词
interactions; mass spectrometry; networks; proteomics; systems biology;
D O I
10.1038/msb.2008.19
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The human protein interaction network will offer global insights into the molecular organization of cells and provide a framework for modeling human disease, but the network's large scale demands new approaches. We report a set of 7000 physical associations among human proteins inferred from indirect evidence: the comparison of human mRNA co-expression patterns with those of orthologous genes in five other eukaryotes, which we demonstrate identifies proteins in the same physical complexes. To evaluate the accuracy of the predicted physical associations, we apply quantitative mass spectrometry shotgun proteomics to measure elution profiles of 3013 human proteins during native biochemical fractionation, demonstrating systematically that putative interaction partners tend to co-sediment. We further validate uncharacterized proteins implicated by the associations in ribosome biogenesis, including WBSCR20C, associated with Williams-Beuren syndrome. This meta-analysis therefore exploits non-protein-based data, but successfully predicts associations, including 5589 novel human physical protein associations, with measured accuracies of 54 +/- 10%, comparable to direct large-scale interaction assays. The new associations' derivation from conserved in vivo phenomena argues strongly for their biological relevance.
引用
收藏
页数:16
相关论文
共 76 条
[11]   Protein interactions - Two methods for assessment of the reliability of high throughput observations [J].
Deane, CM ;
Salwinski, L ;
Xenarios, I ;
Eisenberg, D .
MOLECULAR & CELLULAR PROTEOMICS, 2002, 1 (05) :349-356
[12]   Stress-induced nuclear bodies are sites of accumulation of pre-mRNA processing factors [J].
Denegri, M ;
Chiodi, I ;
Corioni, M ;
Cobianchi, F ;
Riva, S ;
Biamonti, G .
MOLECULAR BIOLOGY OF THE CELL, 2001, 12 (11) :3502-3514
[13]   ACCURATE TRANSCRIPTION INITIATION BY RNA POLYMERASE-II IN A SOLUBLE EXTRACT FROM ISOLATED MAMMALIAN NUCLEI [J].
DIGNAM, JD ;
LEBOVITZ, RM ;
ROEDER, RG .
NUCLEIC ACIDS RESEARCH, 1983, 11 (05) :1475-1489
[14]   Characterization of two novel genes, WBSCR20 and WBSCR22, deleted in Williams-Beuren syndrome [J].
Doll, A ;
Grzeschik, KH .
CYTOGENETICS AND CELL GENETICS, 2001, 95 (1-2) :20-27
[15]   Cluster analysis and display of genome-wide expression patterns [J].
Eisen, MB ;
Spellman, PT ;
Brown, PO ;
Botstein, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (25) :14863-14868
[16]   Large-scale mapping of human protein-protein interactions by mass spectrometry [J].
Ewing, Rob M. ;
Chu, Peter ;
Elisma, Fred ;
Li, Hongyan ;
Taylor, Paul ;
Climie, Shane ;
McBroom-Cerajewski, Linda ;
Robinson, Mark D. ;
O'Connor, Liam ;
Li, Michael ;
Taylor, Rod ;
Dharsee, Moyez ;
Ho, Yuen ;
Heilbut, Adrian ;
Moore, Lynda ;
Zhang, Shudong ;
Ornatsky, Olga ;
Bukhman, Yury V. ;
Ethier, Martin ;
Sheng, Yinglun ;
Vasilescu, Julian ;
Abu-Farha, Mohamed ;
Lambert, Jean-Philippe ;
Duewel, Henry S. ;
Stewart, Ian I. ;
Kuehl, Bonnie ;
Hogue, Kelly ;
Colwill, Karen ;
Gladwish, Katharine ;
Muskat, Brenda ;
Kinach, Robert ;
Adams, Sally-Lin ;
Moran, Michael F. ;
Morin, Gregg B. ;
Topaloglou, Thodoros ;
Figeys, Daniel .
MOLECULAR SYSTEMS BIOLOGY, 2007, 3 (1)
[17]   GRIM-19, a cell death regulatory gene product, is a subunit of bovine mitochondrial NADH:Ubiquinone oxidoreductase (complex I) [J].
Fearnley, IM ;
Carroll, J ;
Shannon, RJ ;
Runswick, MJ ;
Walker, JE ;
Hirst, J .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (42) :38345-38348
[18]   Proteome survey reveals modularity of the yeast cell machinery [J].
Gavin, AC ;
Aloy, P ;
Grandi, P ;
Krause, R ;
Boesche, M ;
Marzioch, M ;
Rau, C ;
Jensen, LJ ;
Bastuck, S ;
Dümpelfeld, B ;
Edelmann, A ;
Heurtier, MA ;
Hoffman, V ;
Hoefert, C ;
Klein, K ;
Hudak, M ;
Michon, AM ;
Schelder, M ;
Schirle, M ;
Remor, M ;
Rudi, T ;
Hooper, S ;
Bauer, A ;
Bouwmeester, T ;
Casari, G ;
Drewes, G ;
Neubauer, G ;
Rick, JM ;
Kuster, B ;
Bork, P ;
Russell, RB ;
Superti-Furga, G .
NATURE, 2006, 440 (7084) :631-636
[19]   Correlation between transcriptome and interactome mapping data from Saccharomyces cerevisiae [J].
Ge, H ;
Liu, ZH ;
Church, GM ;
Vidal, M .
NATURE GENETICS, 2001, 29 (04) :482-486
[20]   Bms1p, a novel GTP-binding protein, and the related Tsr1p are required for distinct steps of 40S ribosome biogenesis in yeast [J].
Gelperin, D ;
Horton, L ;
Beckman, J ;
Hensold, J ;
Lemmon, SK .
RNA, 2001, 7 (09) :1268-1283