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Rewiring of PDZ Domain-Ligand Interaction Network Contributed to Eukaryotic Evolution

PDZ domain-mediated interactions have greatly expanded during metazoan evolution, becoming important for controlling signal flow via the assembly of multiple signaling components. The evolutionary history of PDZ domain-mediated interactions has never been explored at the molecular level. It is of gr...

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Autores principales: Kim, Jinho, Kim, Inhae, Yang, Jae-Seong, Shin, Young-Eun, Hwang, Jihye, Park, Solip, Choi, Yoon Sup, Kim, Sanguk
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3276551/
https://www.ncbi.nlm.nih.gov/pubmed/22346764
http://dx.doi.org/10.1371/journal.pgen.1002510
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author Kim, Jinho
Kim, Inhae
Yang, Jae-Seong
Shin, Young-Eun
Hwang, Jihye
Park, Solip
Choi, Yoon Sup
Kim, Sanguk
author_facet Kim, Jinho
Kim, Inhae
Yang, Jae-Seong
Shin, Young-Eun
Hwang, Jihye
Park, Solip
Choi, Yoon Sup
Kim, Sanguk
author_sort Kim, Jinho
collection PubMed
description PDZ domain-mediated interactions have greatly expanded during metazoan evolution, becoming important for controlling signal flow via the assembly of multiple signaling components. The evolutionary history of PDZ domain-mediated interactions has never been explored at the molecular level. It is of great interest to understand how PDZ domain-ligand interactions emerged and how they become rewired during evolution. Here, we constructed the first human PDZ domain-ligand interaction network (PDZNet) together with binding motif sequences and interaction strengths of ligands. PDZNet includes 1,213 interactions between 97 human PDZ proteins and 591 ligands that connect most PDZ protein-mediated interactions (98%) in a large single network via shared ligands. We examined the rewiring of PDZ domain-ligand interactions throughout eukaryotic evolution by tracing changes in the C-terminal binding motif sequences of the PDZ ligands. We found that interaction rewiring by sequence mutation frequently occurred throughout evolution, largely contributing to the growth of PDZNet. The rewiring of PDZ domain-ligand interactions provided an effective means of functional innovations in nervous system development. Our findings provide empirical evidence for a network evolution model that highlights the rewiring of interactions as a mechanism for the development of new protein functions. PDZNet will be a valuable resource to further characterize the organization of the PDZ domain-mediated signaling proteome.
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spelling pubmed-32765512012-02-15 Rewiring of PDZ Domain-Ligand Interaction Network Contributed to Eukaryotic Evolution Kim, Jinho Kim, Inhae Yang, Jae-Seong Shin, Young-Eun Hwang, Jihye Park, Solip Choi, Yoon Sup Kim, Sanguk PLoS Genet Research Article PDZ domain-mediated interactions have greatly expanded during metazoan evolution, becoming important for controlling signal flow via the assembly of multiple signaling components. The evolutionary history of PDZ domain-mediated interactions has never been explored at the molecular level. It is of great interest to understand how PDZ domain-ligand interactions emerged and how they become rewired during evolution. Here, we constructed the first human PDZ domain-ligand interaction network (PDZNet) together with binding motif sequences and interaction strengths of ligands. PDZNet includes 1,213 interactions between 97 human PDZ proteins and 591 ligands that connect most PDZ protein-mediated interactions (98%) in a large single network via shared ligands. We examined the rewiring of PDZ domain-ligand interactions throughout eukaryotic evolution by tracing changes in the C-terminal binding motif sequences of the PDZ ligands. We found that interaction rewiring by sequence mutation frequently occurred throughout evolution, largely contributing to the growth of PDZNet. The rewiring of PDZ domain-ligand interactions provided an effective means of functional innovations in nervous system development. Our findings provide empirical evidence for a network evolution model that highlights the rewiring of interactions as a mechanism for the development of new protein functions. PDZNet will be a valuable resource to further characterize the organization of the PDZ domain-mediated signaling proteome. Public Library of Science 2012-02-09 /pmc/articles/PMC3276551/ /pubmed/22346764 http://dx.doi.org/10.1371/journal.pgen.1002510 Text en Kim et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Kim, Jinho
Kim, Inhae
Yang, Jae-Seong
Shin, Young-Eun
Hwang, Jihye
Park, Solip
Choi, Yoon Sup
Kim, Sanguk
Rewiring of PDZ Domain-Ligand Interaction Network Contributed to Eukaryotic Evolution
title Rewiring of PDZ Domain-Ligand Interaction Network Contributed to Eukaryotic Evolution
title_full Rewiring of PDZ Domain-Ligand Interaction Network Contributed to Eukaryotic Evolution
title_fullStr Rewiring of PDZ Domain-Ligand Interaction Network Contributed to Eukaryotic Evolution
title_full_unstemmed Rewiring of PDZ Domain-Ligand Interaction Network Contributed to Eukaryotic Evolution
title_short Rewiring of PDZ Domain-Ligand Interaction Network Contributed to Eukaryotic Evolution
title_sort rewiring of pdz domain-ligand interaction network contributed to eukaryotic evolution
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3276551/
https://www.ncbi.nlm.nih.gov/pubmed/22346764
http://dx.doi.org/10.1371/journal.pgen.1002510
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