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A reference map of the human binary protein interactome.

Authors :
Luck K
Kim DK
Lambourne L
Spirohn K
Begg BE
Bian W
Brignall R
Cafarelli T
Campos-Laborie FJ
Charloteaux B
Choi D
Coté AG
Daley M
Deimling S
Desbuleux A
Dricot A
Gebbia M
Hardy MF
Kishore N
Knapp JJ
Kovács IA
Lemmens I
Mee MW
Mellor JC
Pollis C
Pons C
Richardson AD
Schlabach S
Teeking B
Yadav A
Babor M
Balcha D
Basha O
Bowman-Colin C
Chin SF
Choi SG
Colabella C
Coppin G
D'Amata C
De Ridder D
De Rouck S
Duran-Frigola M
Ennajdaoui H
Goebels F
Goehring L
Gopal A
Haddad G
Hatchi E
Helmy M
Jacob Y
Kassa Y
Landini S
Li R
van Lieshout N
MacWilliams A
Markey D
Paulson JN
Rangarajan S
Rasla J
Rayhan A
Rolland T
San-Miguel A
Shen Y
Sheykhkarimli D
Sheynkman GM
Simonovsky E
Taşan M
Tejeda A
Tropepe V
Twizere JC
Wang Y
Weatheritt RJ
Weile J
Xia Y
Yang X
Yeger-Lotem E
Zhong Q
Aloy P
Bader GD
De Las Rivas J
Gaudet S
Hao T
Rak J
Tavernier J
Hill DE
Vidal M
Roth FP
Calderwood MA
Source :
Nature [Nature] 2020 Apr; Vol. 580 (7803), pp. 402-408. Date of Electronic Publication: 2020 Apr 08.
Publication Year :
2020

Abstract

Global insights into cellular organization and genome function require comprehensive understanding of the interactome networks that mediate genotype-phenotype relationships <superscript>1,2</superscript> . Here we present a human 'all-by-all' reference interactome map of human binary protein interactions, or 'HuRI'. With approximately 53,000 protein-protein interactions, HuRI has approximately four times as many such interactions as there are high-quality curated interactions from small-scale studies. The integration of HuRI with genome <superscript>3</superscript> , transcriptome <superscript>4</superscript> and proteome <superscript>5</superscript> data enables cellular function to be studied within most physiological or pathological cellular contexts. We demonstrate the utility of HuRI in identifying the specific subcellular roles of protein-protein interactions. Inferred tissue-specific networks reveal general principles for the formation of cellular context-specific functions and elucidate potential molecular mechanisms that might underlie tissue-specific phenotypes of Mendelian diseases. HuRI is a systematic proteome-wide reference that links genomic variation to phenotypic outcomes.

Details

Language :
English
ISSN :
1476-4687
Volume :
580
Issue :
7803
Database :
MEDLINE
Journal :
Nature
Publication Type :
Academic Journal
Accession number :
32296183
Full Text :
https://doi.org/10.1038/s41586-020-2188-x