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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Research Foundation
2012
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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. |
format | Online Article Text |
id | pubmed-3422896 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Frontiers Research Foundation |
record_format | MEDLINE/PubMed |
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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