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Tetramer formation in Arabidopsis MADS domain proteins: analysis of a protein-protein interaction network

BACKGROUND: MADS domain proteins are transcription factors that coordinate several important developmental processes in plants. These proteins interact with other MADS domain proteins to form dimers, and it has been proposed that they are able to associate as tetrameric complexes that regulate trans...

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Autores principales: Espinosa-Soto, Carlos, Immink, Richard GH, Angenent, Gerco C, Alvarez-Buylla, Elena R, de Folter, Stefan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3913338/
https://www.ncbi.nlm.nih.gov/pubmed/24468197
http://dx.doi.org/10.1186/1752-0509-8-9
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author Espinosa-Soto, Carlos
Immink, Richard GH
Angenent, Gerco C
Alvarez-Buylla, Elena R
de Folter, Stefan
author_facet Espinosa-Soto, Carlos
Immink, Richard GH
Angenent, Gerco C
Alvarez-Buylla, Elena R
de Folter, Stefan
author_sort Espinosa-Soto, Carlos
collection PubMed
description BACKGROUND: MADS domain proteins are transcription factors that coordinate several important developmental processes in plants. These proteins interact with other MADS domain proteins to form dimers, and it has been proposed that they are able to associate as tetrameric complexes that regulate transcription of target genes. Whether the formation of functional tetramers is a widespread property of plant MADS domain proteins, or it is specific to few of these transcriptional regulators remains unclear. RESULTS: We analyzed the structure of the network of physical interactions among MADS domain proteins in Arabidopsis thaliana. We determined the abundance of subgraphs that represent the connection pattern expected for a MADS domain protein heterotetramer. These subgraphs were significantly more abundant in the MADS domain protein interaction network than in randomized analogous networks. Importantly, these subgraphs are not significantly frequent in a protein interaction network of TCP plant transcription factors, when compared to expectation by chance. In addition, we found that MADS domain proteins in tetramer-like subgraphs are more likely to be expressed jointly than proteins in other subgraphs. This effect is mainly due to proteins in the monophyletic MIKC clade, as there is no association between tetramer-like subgraphs and co-expression for proteins outside this clade. CONCLUSIONS: Our results support that the tendency to form functional tetramers is widespread in the MADS domain protein-protein interaction network. Our observations also suggest that this trend is prevalent, or perhaps exclusive, for proteins in the MIKC clade. Because it is possible to retrodict several experimental results from our analyses, our work can be an important aid to make new predictions and facilitates experimental research on plant MADS domain proteins.
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spelling pubmed-39133382014-02-14 Tetramer formation in Arabidopsis MADS domain proteins: analysis of a protein-protein interaction network Espinosa-Soto, Carlos Immink, Richard GH Angenent, Gerco C Alvarez-Buylla, Elena R de Folter, Stefan BMC Syst Biol Research Article BACKGROUND: MADS domain proteins are transcription factors that coordinate several important developmental processes in plants. These proteins interact with other MADS domain proteins to form dimers, and it has been proposed that they are able to associate as tetrameric complexes that regulate transcription of target genes. Whether the formation of functional tetramers is a widespread property of plant MADS domain proteins, or it is specific to few of these transcriptional regulators remains unclear. RESULTS: We analyzed the structure of the network of physical interactions among MADS domain proteins in Arabidopsis thaliana. We determined the abundance of subgraphs that represent the connection pattern expected for a MADS domain protein heterotetramer. These subgraphs were significantly more abundant in the MADS domain protein interaction network than in randomized analogous networks. Importantly, these subgraphs are not significantly frequent in a protein interaction network of TCP plant transcription factors, when compared to expectation by chance. In addition, we found that MADS domain proteins in tetramer-like subgraphs are more likely to be expressed jointly than proteins in other subgraphs. This effect is mainly due to proteins in the monophyletic MIKC clade, as there is no association between tetramer-like subgraphs and co-expression for proteins outside this clade. CONCLUSIONS: Our results support that the tendency to form functional tetramers is widespread in the MADS domain protein-protein interaction network. Our observations also suggest that this trend is prevalent, or perhaps exclusive, for proteins in the MIKC clade. Because it is possible to retrodict several experimental results from our analyses, our work can be an important aid to make new predictions and facilitates experimental research on plant MADS domain proteins. BioMed Central 2014-01-27 /pmc/articles/PMC3913338/ /pubmed/24468197 http://dx.doi.org/10.1186/1752-0509-8-9 Text en Copyright © 2014 Espinosa-Soto et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Espinosa-Soto, Carlos
Immink, Richard GH
Angenent, Gerco C
Alvarez-Buylla, Elena R
de Folter, Stefan
Tetramer formation in Arabidopsis MADS domain proteins: analysis of a protein-protein interaction network
title Tetramer formation in Arabidopsis MADS domain proteins: analysis of a protein-protein interaction network
title_full Tetramer formation in Arabidopsis MADS domain proteins: analysis of a protein-protein interaction network
title_fullStr Tetramer formation in Arabidopsis MADS domain proteins: analysis of a protein-protein interaction network
title_full_unstemmed Tetramer formation in Arabidopsis MADS domain proteins: analysis of a protein-protein interaction network
title_short Tetramer formation in Arabidopsis MADS domain proteins: analysis of a protein-protein interaction network
title_sort tetramer formation in arabidopsis mads domain proteins: analysis of a protein-protein interaction network
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3913338/
https://www.ncbi.nlm.nih.gov/pubmed/24468197
http://dx.doi.org/10.1186/1752-0509-8-9
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