A protein interaction map of Drosophila melanogaster

被引:1704
作者
Giot, L
Bader, JS
Brouwer, C
Chaudhuri, A
Kuang, B
Li, Y
Hao, YL
Ooi, CE
Godwin, B
Vitols, E
Vijayadamodar, G
Pochart, P
Machineni, H
Welsh, M
Kong, Y
Zerhusen, B
Malcolm, R
Varrone, Z
Collis, A
Minto, M
Burgess, S
McDaniel, L
Stimpson, E
Spriggs, F
Williams, J
Neurath, K
Ioime, N
Agee, M
Voss, E
Furtak, K
Renzulli, R
Aanensen, N
Carrolla, S
Bickelhaupt, E
Lazovatsky, Y
DaSilva, A
Zhong, J
Stanyon, CA
Finley, RL
White, KP
Braverman, M
Jarvie, T
Gold, S
Leach, M
Knight, J
Shimkets, RA
McKenna, MP
Chant, J
Rothberg, JM
机构
[1] GuraGen Corp, New Haven, CT 06511 USA
[2] Wayne State Univ, Sch Med, Ctr Mol Med & Genet, Detroit, MI 48201 USA
[3] Yale Univ, Sch Med, Dept Genet, New Haven, CT 06520 USA
关键词
D O I
10.1126/science.1090289
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Drosophila melanogaster is a proven model system for many aspects of human biology. Here we present a two-hybrid-based protein-interaction map of the fly proteome. A total of 10,623 predicted transcripts were isolated and screened against standard and normalized complementary DNA libraries to produce a draft map of 7048 proteins and 20,405 interactions. A computational method of rating two-hybrid interaction confidence was developed to re. ne this draft map to a higher confidence map of 4679 proteins and 4780 interactions. Statistical modeling of the network showed two levels of organization: a short-range organization, presumably corresponding to multiprotein complexes, and a more global organization, presumably corresponding to intercomplex connections. The network recapitulated known pathways, extended pathways, and uncovered previously unknown pathway components. This map serves as a starting point for a systems biology modeling of multicellular organisms, including humans.
引用
收藏
页码:1727 / 1736
页数:10
相关论文
共 58 条
[1]   The genome sequence of Drosophila melanogaster [J].
Adams, MD ;
Celniker, SE ;
Holt, RA ;
Evans, CA ;
Gocayne, JD ;
Amanatides, PG ;
Scherer, SE ;
Li, PW ;
Hoskins, RA ;
Galle, RF ;
George, RA ;
Lewis, SE ;
Richards, S ;
Ashburner, M ;
Henderson, SN ;
Sutton, GG ;
Wortman, JR ;
Yandell, MD ;
Zhang, Q ;
Chen, LX ;
Brandon, RC ;
Rogers, YHC ;
Blazej, RG ;
Champe, M ;
Pfeiffer, BD ;
Wan, KH ;
Doyle, C ;
Baxter, EG ;
Helt, G ;
Nelson, CR ;
Miklos, GLG ;
Abril, JF ;
Agbayani, A ;
An, HJ ;
Andrews-Pfannkoch, C ;
Baldwin, D ;
Ballew, RM ;
Basu, A ;
Baxendale, J ;
Bayraktaroglu, L ;
Beasley, EM ;
Beeson, KY ;
Benos, PV ;
Berman, BP ;
Bhandari, D ;
Bolshakov, S ;
Borkova, D ;
Botchan, MR ;
Bouck, J ;
Brokstein, P .
SCIENCE, 2000, 287 (5461) :2185-2195
[2]   G-patch: a new conserved domain in eukaryotic RNA-processing proteins and type D retroviral polyproteins [J].
Aravind, L ;
Koonin, EV .
TRENDS IN BIOCHEMICAL SCIENCES, 1999, 24 (09) :342-344
[3]   Gene Ontology: tool for the unification of biology [J].
Ashburner, M ;
Ball, CA ;
Blake, JA ;
Botstein, D ;
Butler, H ;
Cherry, JM ;
Davis, AP ;
Dolinski, K ;
Dwight, SS ;
Eppig, JT ;
Harris, MA ;
Hill, DP ;
Issel-Tarver, L ;
Kasarskis, A ;
Lewis, S ;
Matese, JC ;
Richardson, JE ;
Ringwald, M ;
Rubin, GM ;
Sherlock, G .
NATURE GENETICS, 2000, 25 (01) :25-29
[4]  
BADER JS, IN PRESS NATURE BIOT
[5]   SKP1 connects cell cycle regulators to the ubiquitin proteolysis machinery through a novel motif, the F-box [J].
Bai, C ;
Sen, P ;
Hofmann, K ;
Ma, L ;
Goebl, M ;
Harper, JW ;
Elledge, SJ .
CELL, 1996, 86 (02) :263-274
[6]   Emergence of scaling in random networks [J].
Barabási, AL ;
Albert, R .
SCIENCE, 1999, 286 (5439) :509-512
[7]   IDENTIFICATION OF THE GENE ASSOCIATED WITH THE RECURRING CHROMOSOMAL TRANSLOCATIONS T(3,14)(Q27,Q32) AND T(3,22)(Q27,Q11) IN B-CELL LYMPHOMAS [J].
BARON, BW ;
NUCIFORA, G ;
MCCABE, N ;
ESPINOSA, R ;
LEBEAU, MM ;
MCKEITHAN, TW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (11) :5262-5266
[8]   Two new substrates in insulin signaling, IRS5/DOK4 and IRS6/DOK5 [J].
Cai, DS ;
Dhe-Paganon, S ;
Melendez, PA ;
Lee, JS ;
Shoelson, SE .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (28) :25323-25330
[9]   The damage-responsive Drosophila gene sickle encodes a novel IAP binding protein similar to but distinct from reaper, grim, and hid [J].
Christich, A ;
Kauppila, S ;
Chen, P ;
Sogame, N ;
Ho, SI ;
Abrams, JM .
CURRENT BIOLOGY, 2002, 12 (02) :137-140
[10]  
Courey AJ, 2001, GENE DEV, V15, P2786