Next-generation large-scale binary protein interaction network for Drosophila melanogaster

被引:11
|
作者
Tang, Hong-Wen [1 ,2 ,3 ]
Spirohn, Kerstin [1 ,4 ]
Hu, Yanhui [1 ]
Hao, Tong [1 ,4 ]
Kovacs, Istvan A. [4 ,5 ,6 ]
Gao, Yue [1 ]
Binari, Richard [1 ,7 ]
Yang-Zhou, Donghui [1 ]
Wan, Kenneth H. [8 ]
Bader, Joel S. [9 ,10 ]
Balcha, Dawit [1 ,4 ]
Bian, Wenting [1 ,4 ]
Booth, Benjamin W. [8 ]
Cote, Atina G. [4 ,11 ]
de Rouck, Steffi
Desbuleux, Alice [1 ,4 ]
Goh, Kah Yong [2 ]
Kim, Dae-Kyum
Knapp, Jennifer J. [11 ]
Lee, Wen Xing [2 ]
Lemmens, Irma
Li, Cathleen [1 ]
Li, Mian [1 ]
Li, Roujia [4 ,11 ]
Lim, Hyobin Julianne
Liu, Yifang [1 ]
Luck, Katja [1 ,4 ]
Markey, Dylan [1 ,4 ]
Pollis, Carl [1 ,4 ]
Rangarajan, Sudharshan [1 ,4 ]
Rodiger, Jonathan [1 ]
Schlabach, Sadie [1 ,4 ]
Shen, Yun [1 ,4 ]
Sheykhkarimli, Dayag [4 ,11 ]
TeeKing, Bridget [1 ,4 ]
Roth, Frederick P. [4 ,11 ]
Tavernier, Jan
Calderwood, Michael A. [1 ,4 ]
Hill, David E. [1 ,4 ]
Celniker, Susan E. [8 ]
Vidal, Marc [1 ,4 ]
Perrimon, Norbert [1 ,7 ]
Mohr, Stephanie E. [1 ]
机构
[1] Harvard Med Sch, Blavatnik Inst, Dept Genet, 77 Ave Louis Pasteur, Boston, MA 02115 USA
[2] Duke NUS Med Sch, Program Canc & Stem Cell Biol, 8 Coll Rd, Singapore 169857, Singapore
[3] Humphrey Oei Inst Canc Res, Natl Canc Ctr Singapore, Div Cellular & Mol Res, Singapore 169610, Singapore
[4] Dana Farber Canc Inst, Ctr Canc Syst Biol CCSB, 450 Brookline Ave, Boston, MA 02215 USA
[5] Northwestern Univ, Dept Phys & Astron, 633 Clark St, Evanston, IL 60208 USA
[6] Northwestern Univ, Northwestern Inst Complex Syst, Chambers Hall,600 Foster St, Evanston, IL 60208 USA
[7] Howard Hughes Med Inst, 77 Ave Louis Pasteur, Boston, MA 02115 USA
[8] Lawrence Berkeley Natl Lab, Berkeley Drosophila Genome Project, 1 Cyclotron Rd, Berkeley, CA 94720 USA
[9] Johns Hopkins Univ, Whiting Sch Engn, Dept Biomed Engn, 3400 North Charles St, Baltimore, MD 21218 USA
[10] Johns Hopkins Sch Med, Inst Basic Biol Sci, High Throughput Biol Ctr, 733 North Broadway, Baltimore, MD 21205 USA
[11] Univ Toronto, Dept Mol Genet, 160 Coll St, Toronto, ON M5S 3E1, Canada
基金
加拿大健康研究院;
关键词
INTERACTION MAP; TRANSCRIPTION FACTOR; INTEGRATED RESOURCE; CELL-DEATH; AUTOPHAGY; GENE; SEQUENCE; ELEMENTS; DATABASE; DESIGN;
D O I
10.1038/s41467-023-37876-0
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
Maps of protein-protein interactions (PPIs) help identify new components of pathways, complexes, and processes. In this work, state-of-the-art methods are used to identify binary Drosophila PPIs, generating broadly useful physical and data resources. Generating reference maps of interactome networks illuminates genetic studies by providing a protein-centric approach to finding new components of existing pathways, complexes, and processes. We apply state-of-the-art methods to identify binary protein-protein interactions (PPIs) for Drosophila melanogaster. Four all-by-all yeast two-hybrid (Y2H) screens of > 10,000 Drosophila proteins result in the 'FlyBi' dataset of 8723 PPIs among 2939 proteins. Testing subsets of data from FlyBi and previous PPI studies using an orthogonal assay allows for normalization of data quality; subsequent integration of FlyBi and previous data results in an expanded binary Drosophila reference interaction network, DroRI, comprising 17,232 interactions among 6511 proteins. We use FlyBi data to generate an autophagy network, then validate in vivo using autophagy-related assays. The deformed wings (dwg) gene encodes a protein that is both a regulator and a target of autophagy. Altogether, these resources provide a foundation for building new hypotheses regarding protein networks and function.
引用
收藏
页数:16
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