TY - JOUR
T1 - A comprehensive resource of interacting protein regions for refining human transcription factor networks
AU - Miyamoto-Sato, Etsuko
AU - Fujimori, Shigeo
AU - Ishizaka, Masamichi
AU - Hirai, Naoya
AU - Masuoka, Kazuyo
AU - Saito, Rintaro
AU - Ozawa, Yosuke
AU - Hino, Katsuya
AU - Washio, Takanori
AU - Tomita, Masaru
AU - Yamashita, Tatsuhiro
AU - Oshikubo, Tomohiro
AU - Akasaka, Hidetoshi
AU - Sugiyama, Jun
AU - Matsumoto, Yasuo
AU - Yanagawa, Hiroshi
PY - 2010/2/24
Y1 - 2010/2/24
N2 - Large-scale data sets of protein-protein interactions (PPIs) are a valuable resource for mapping and analysis of the topological and dynamic features of interactome networks. The currently available large-scale PPI data sets only contain information on interaction partners. The data presented in this study also include the sequences involved in the interactions (i.e., the interacting regions, IRs) suggested to correspond to functional and structural domains. Here we present the first large-scale IR data set obtained using mRNA display for 50 human transcription factors (TFs), including 12 transcription-related proteins. The core data set (966 IRs; 943 PPIs) displays a verification rate of 70%. Analysis of the IR data set revealed the existence of IRs that interact with multiple partners. Furthermore, these IRs were preferentially associated with intrinsic disorder. This finding supports the hypothesis that intrinsically disordered regions play a major role in the dynamics and diversity of TF networks through their ability to structurally adapt to and bind with multiple partners. Accordingly, this domain-based interaction resource represents an important step in refining protein interactions and networks at the domain level and in associating network analysis with biological structure and function.
AB - Large-scale data sets of protein-protein interactions (PPIs) are a valuable resource for mapping and analysis of the topological and dynamic features of interactome networks. The currently available large-scale PPI data sets only contain information on interaction partners. The data presented in this study also include the sequences involved in the interactions (i.e., the interacting regions, IRs) suggested to correspond to functional and structural domains. Here we present the first large-scale IR data set obtained using mRNA display for 50 human transcription factors (TFs), including 12 transcription-related proteins. The core data set (966 IRs; 943 PPIs) displays a verification rate of 70%. Analysis of the IR data set revealed the existence of IRs that interact with multiple partners. Furthermore, these IRs were preferentially associated with intrinsic disorder. This finding supports the hypothesis that intrinsically disordered regions play a major role in the dynamics and diversity of TF networks through their ability to structurally adapt to and bind with multiple partners. Accordingly, this domain-based interaction resource represents an important step in refining protein interactions and networks at the domain level and in associating network analysis with biological structure and function.
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U2 - 10.1371/journal.pone.0009289
DO - 10.1371/journal.pone.0009289
M3 - Article
C2 - 20195357
AN - SCOPUS:77949762977
SN - 1932-6203
VL - 5
JO - PloS one
JF - PloS one
IS - 2
M1 - e9289
ER -