Towards a proteome-scale map of the human protein-protein interaction network

被引:2138
作者
Rual, JF
Venkatesan, K
Hao, T
Hirozane-Kishikawa, T
Dricot, A
Li, N
Berriz, GF
Gibbons, FD
Dreze, M
Ayivi-Guedehoussou, N
Klitgord, N
Simon, C
Boxem, M
Milstein, S
Rosenberg, J
Goldberg, DS
Zhang, LV
Wong, SL
Franklin, G
Li, SM
Albala, JS
Lim, JH
Fraughton, C
Llamosas, E
Cevik, S
Bex, C
Lamesch, P
Sikorski, RS
Vandenhaute, J
Zoghbi, HY
Smolyar, A
Bosak, S
Sequerra, R
Doucette-Stamm, L
Cusick, ME
Hill, DE
Roth, FP
Vidal, M
机构
[1] Dana Farber Canc Inst, Ctr Canc Syst Biol, Boston, MA 02115 USA
[2] Dana Farber Canc Inst, Dept Canc Biol, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Dept Genet, Boston, MA 02115 USA
[4] Harvard Univ, Sch Med, Dept Biol Chem & Mol Pharmacol, Boston, MA 02115 USA
[5] Fac Notre Dame Paix, Unite Rech Biol Mol, B-5000 Namur, Belgium
[6] Howard Hughes Med Inst, Houston, TX 77030 USA
[7] Baylor Univ, Dept Pediat, Houston, TX 77030 USA
[8] Baylor Univ, Dept Neurol, Houston, TX 77030 USA
[9] Baylor Univ, Dept Neurosci, Houston, TX 77030 USA
[10] Baylor Univ, Dept Mol & Human Genet, Houston, TX 77030 USA
[11] Arcbay Inc, Boston, MA 01915 USA
[12] Agencourt Biosci Corp, Beverly, MA 01915 USA
关键词
D O I
10.1038/nature04209
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
Systematic mapping of protein-protein interactions, or 'interactome' mapping, was initiated in model organisms, starting with defined biological processes(1,2) and then expanding to the scale of the proteome(3-7). Although far from complete, such maps have revealed global topological and dynamic features of interactome networks that relate to known biological properties(8,9), suggesting that a human interactome map will provide insight into development and disease mechanisms at a systems level. Here we describe an initial version of a proteome-scale map of human binary protein-protein interactions. Using a stringent, high-throughput yeast two-hybrid system, we tested pairwise interactions among the products of similar to 8,100 currently available Gateway-cloned open reading frames and detected similar to 2,800 interactions. This data set, called CCSB-HI1, has a verification rate of similar to 78% as revealed by an independent co-affinity purification assay, and correlates significantly with other biological attributes. The CCSB-HI1 data set increases by similar to 70% the set of available binary interactions within the tested space and reveals more than 300 new connections to over 100 disease-associated proteins. This work represents an important step towards a systematic and comprehensive human interactome project.
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收藏
页码:1173 / 1178
页数:6
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