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14-3-3 phosphoprotein interaction networks – does isoform diversity present functional interaction specification?

The 14-3-3 proteins have emerged as major phosphoprotein interaction proteins and thereby constitute a key node in the Arabidopsis Interactome Map, a node through which a large number of important signals pass. Throughout their history of discovery and description, the 14-3-3s have been described as...

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Autores principales: Paul, Anna-Lisa, Denison, Fiona C., Schultz, Eric R., Zupanska, Agata K., Ferl, Robert J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Research Foundation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3422896/
https://www.ncbi.nlm.nih.gov/pubmed/22934100
http://dx.doi.org/10.3389/fpls.2012.00190
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author Paul, Anna-Lisa
Denison, Fiona C.
Schultz, Eric R.
Zupanska, Agata K.
Ferl, Robert J.
author_facet Paul, Anna-Lisa
Denison, Fiona C.
Schultz, Eric R.
Zupanska, Agata K.
Ferl, Robert J.
author_sort Paul, Anna-Lisa
collection PubMed
description The 14-3-3 proteins have emerged as major phosphoprotein interaction proteins and thereby constitute a key node in the Arabidopsis Interactome Map, a node through which a large number of important signals pass. Throughout their history of discovery and description, the 14-3-3s have been described as protein families and there has been some evidence that the different 14-3-3 family members within any organism might carry isoform-specific functions. However, there has also been evidence for redundancy of 14-3-3 function, suggesting that the perceived 14-3-3 diversity may be the accumulation of neutral mutations over evolutionary time and as some 14-3-3 genes develop tissue or organ-specific expression. This situation has led to a currently unresolved question – does 14-3-3 isoform sequence diversity indicate functional diversity at the biochemical or cellular level? We discuss here some of the key observations on both sides of the resulting debate, and present a set of contrastable observations to address the theory functional diversity does exist among 14-3-3 isoforms. The resulting model suggests strongly that there are indeed functional specificities in the 14-3-3s of Arabidopsis. The model further suggests that 14-3-3 diversity and specificity should enter into the discussion of 14-3-3 roles in signal transduction and be directly approached in 14-3-3 experimentation. It is hoped that future studies involving 14-3-3s will continue to address specificity in experimental design and analysis.
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spelling pubmed-34228962012-08-29 14-3-3 phosphoprotein interaction networks – does isoform diversity present functional interaction specification? Paul, Anna-Lisa Denison, Fiona C. Schultz, Eric R. Zupanska, Agata K. Ferl, Robert J. Front Plant Sci Plant Science The 14-3-3 proteins have emerged as major phosphoprotein interaction proteins and thereby constitute a key node in the Arabidopsis Interactome Map, a node through which a large number of important signals pass. Throughout their history of discovery and description, the 14-3-3s have been described as protein families and there has been some evidence that the different 14-3-3 family members within any organism might carry isoform-specific functions. However, there has also been evidence for redundancy of 14-3-3 function, suggesting that the perceived 14-3-3 diversity may be the accumulation of neutral mutations over evolutionary time and as some 14-3-3 genes develop tissue or organ-specific expression. This situation has led to a currently unresolved question – does 14-3-3 isoform sequence diversity indicate functional diversity at the biochemical or cellular level? We discuss here some of the key observations on both sides of the resulting debate, and present a set of contrastable observations to address the theory functional diversity does exist among 14-3-3 isoforms. The resulting model suggests strongly that there are indeed functional specificities in the 14-3-3s of Arabidopsis. The model further suggests that 14-3-3 diversity and specificity should enter into the discussion of 14-3-3 roles in signal transduction and be directly approached in 14-3-3 experimentation. It is hoped that future studies involving 14-3-3s will continue to address specificity in experimental design and analysis. Frontiers Research Foundation 2012-08-20 /pmc/articles/PMC3422896/ /pubmed/22934100 http://dx.doi.org/10.3389/fpls.2012.00190 Text en Copyright © Paul, Denison, Schultz, Zupanska and Ferl. http://www.frontiersin.org/licenseagreement This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) , which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc.
spellingShingle Plant Science
Paul, Anna-Lisa
Denison, Fiona C.
Schultz, Eric R.
Zupanska, Agata K.
Ferl, Robert J.
14-3-3 phosphoprotein interaction networks – does isoform diversity present functional interaction specification?
title 14-3-3 phosphoprotein interaction networks – does isoform diversity present functional interaction specification?
title_full 14-3-3 phosphoprotein interaction networks – does isoform diversity present functional interaction specification?
title_fullStr 14-3-3 phosphoprotein interaction networks – does isoform diversity present functional interaction specification?
title_full_unstemmed 14-3-3 phosphoprotein interaction networks – does isoform diversity present functional interaction specification?
title_short 14-3-3 phosphoprotein interaction networks – does isoform diversity present functional interaction specification?
title_sort 14-3-3 phosphoprotein interaction networks – does isoform diversity present functional interaction specification?
topic Plant Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3422896/
https://www.ncbi.nlm.nih.gov/pubmed/22934100
http://dx.doi.org/10.3389/fpls.2012.00190
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