TY - JOUR
T1 - Global analysis of phosphorylation networks in humans
AU - Hu, Jianfei
AU - Rho, Hee-Sool
AU - Newman, Robert H.
AU - Hwang, Woochang
AU - Neiswinger, John
AU - Zhu, Heng
AU - Zhang, Jin
AU - Qian, Jiang
N1 - Funding Information:
This work is supported in part by the NIH grants ( R01 DK073368 and DP1 OD006419 to JZ; R01 GM076102 to HZ; R21 EY021897 to JQ).
PY - 2014/1
Y1 - 2014/1
N2 - Phosphorylation-mediated signaling plays a crucial role in nearly every aspect of cellular physiology. A recent study based on protein microarray experiments identified a large number of kinase-substrate relationships (KSRs), and built a comprehensive and reliable phosphorylation network in humans. Analysis of this network, in conjunction with additional resources, revealed several key features. First, comparison of the human and yeast phosphorylation networks uncovered an evolutionarily conserved signaling backbone dominated by kinase-to-kinase relationships. Second, although most of the KSRs themselves are not conserved, the functions enriched in the substrates for a given kinase are often conserved. Third, the prevalence of kinase-transcription factor regulatory modules suggests that phosphorylation and transcriptional regulatory networks are inherently wired together to form integrated regulatory circuits. Overall, the phosphorylation networks described in this work promise to offer new insights into the properties of kinase signaling pathways, at both the global and the protein levels. This article is part of a Special Issue entitled: Computational Proteomics, Systems Biology & Clinical Implications. Guest Editor: Yudong Cai.
AB - Phosphorylation-mediated signaling plays a crucial role in nearly every aspect of cellular physiology. A recent study based on protein microarray experiments identified a large number of kinase-substrate relationships (KSRs), and built a comprehensive and reliable phosphorylation network in humans. Analysis of this network, in conjunction with additional resources, revealed several key features. First, comparison of the human and yeast phosphorylation networks uncovered an evolutionarily conserved signaling backbone dominated by kinase-to-kinase relationships. Second, although most of the KSRs themselves are not conserved, the functions enriched in the substrates for a given kinase are often conserved. Third, the prevalence of kinase-transcription factor regulatory modules suggests that phosphorylation and transcriptional regulatory networks are inherently wired together to form integrated regulatory circuits. Overall, the phosphorylation networks described in this work promise to offer new insights into the properties of kinase signaling pathways, at both the global and the protein levels. This article is part of a Special Issue entitled: Computational Proteomics, Systems Biology & Clinical Implications. Guest Editor: Yudong Cai.
KW - Conservation
KW - Kinase-substrate relationships (KSRs)
KW - Network module
KW - Phosphorylation network
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U2 - 10.1016/j.bbapap.2013.03.009
DO - 10.1016/j.bbapap.2013.03.009
M3 - Article
C2 - 23524292
AN - SCOPUS:84890130120
SN - 1570-9639
VL - 1844
SP - 224
EP - 231
JO - Biochimica et Biophysica Acta - Proteins and Proteomics
JF - Biochimica et Biophysica Acta - Proteins and Proteomics
IS - 1 PART B
ER -