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A comparative study of Whi5 and retinoblastoma proteins: from sequence and structure analysis to intracellular networks

Cell growth and proliferation require a complex series of tight-regulated and well-orchestrated events. Accordingly, proteins governing such events are evolutionary conserved, even among distant organisms. By contrast, it is more singular the case of “core functions” exerted by functional analogous...

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Autores principales: Hasan, Md Mehedi, Brocca, Stefania, Sacco, Elena, Spinelli, Michela, Papaleo, Elena, Lambrughi, Matteo, Alberghina, Lilia, Vanoni, Marco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3897220/
https://www.ncbi.nlm.nih.gov/pubmed/24478706
http://dx.doi.org/10.3389/fphys.2013.00315
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author Hasan, Md Mehedi
Brocca, Stefania
Sacco, Elena
Spinelli, Michela
Papaleo, Elena
Lambrughi, Matteo
Alberghina, Lilia
Vanoni, Marco
author_facet Hasan, Md Mehedi
Brocca, Stefania
Sacco, Elena
Spinelli, Michela
Papaleo, Elena
Lambrughi, Matteo
Alberghina, Lilia
Vanoni, Marco
author_sort Hasan, Md Mehedi
collection PubMed
description Cell growth and proliferation require a complex series of tight-regulated and well-orchestrated events. Accordingly, proteins governing such events are evolutionary conserved, even among distant organisms. By contrast, it is more singular the case of “core functions” exerted by functional analogous proteins that are not homologous and do not share any kind of structural similarity. This is the case of proteins regulating the G1/S transition in higher eukaryotes–i.e., the retinoblastoma (Rb) tumor suppressor Rb—and budding yeast, i.e., Whi5. The interaction landscape of Rb and Whi5 is quite large, with more than one hundred proteins interacting either genetically or physically with each protein. The Whi5 interactome has been used to construct a concept map of Whi5 function and regulation. Comparison of physical and genetic interactors of Rb and Whi5 allows highlighting a significant core of conserved, common functionalities associated with the interactors indicating that structure and function of the network—rather than individual proteins—are conserved during evolution. A combined bioinformatics and biochemical approach has shown that the whole Whi5 protein is highly disordered, except for a small region containing the protein family signature. The comparison with Whi5 homologs from Saccharomycetales has prompted the hypothesis of a modular organization of structural disorder, with most evolutionary conserved regions alternating with highly variable ones. The finding of a consensus sequence points to the conservation of a specific phosphorylation rhythm along with two disordered sequence motifs, probably acting as phosphorylation-dependent seeds in Whi5 folding/unfolding. Thus, the widely disordered Whi5 appears to act as a hierarchical, “date hub” that has evolutionary assayed an original way of modular organization before being supplanted by the globular, multi-domain structured Rb, more suitable to cover the role of a “party hub”.
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spelling pubmed-38972202014-01-29 A comparative study of Whi5 and retinoblastoma proteins: from sequence and structure analysis to intracellular networks Hasan, Md Mehedi Brocca, Stefania Sacco, Elena Spinelli, Michela Papaleo, Elena Lambrughi, Matteo Alberghina, Lilia Vanoni, Marco Front Physiol Physiology Cell growth and proliferation require a complex series of tight-regulated and well-orchestrated events. Accordingly, proteins governing such events are evolutionary conserved, even among distant organisms. By contrast, it is more singular the case of “core functions” exerted by functional analogous proteins that are not homologous and do not share any kind of structural similarity. This is the case of proteins regulating the G1/S transition in higher eukaryotes–i.e., the retinoblastoma (Rb) tumor suppressor Rb—and budding yeast, i.e., Whi5. The interaction landscape of Rb and Whi5 is quite large, with more than one hundred proteins interacting either genetically or physically with each protein. The Whi5 interactome has been used to construct a concept map of Whi5 function and regulation. Comparison of physical and genetic interactors of Rb and Whi5 allows highlighting a significant core of conserved, common functionalities associated with the interactors indicating that structure and function of the network—rather than individual proteins—are conserved during evolution. A combined bioinformatics and biochemical approach has shown that the whole Whi5 protein is highly disordered, except for a small region containing the protein family signature. The comparison with Whi5 homologs from Saccharomycetales has prompted the hypothesis of a modular organization of structural disorder, with most evolutionary conserved regions alternating with highly variable ones. The finding of a consensus sequence points to the conservation of a specific phosphorylation rhythm along with two disordered sequence motifs, probably acting as phosphorylation-dependent seeds in Whi5 folding/unfolding. Thus, the widely disordered Whi5 appears to act as a hierarchical, “date hub” that has evolutionary assayed an original way of modular organization before being supplanted by the globular, multi-domain structured Rb, more suitable to cover the role of a “party hub”. Frontiers Media S.A. 2014-01-21 /pmc/articles/PMC3897220/ /pubmed/24478706 http://dx.doi.org/10.3389/fphys.2013.00315 Text en Copyright © 2014 Hasan, Brocca, Sacco, Spinelli, Papaleo, Lambrughi, Alberghina and Vanoni. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Physiology
Hasan, Md Mehedi
Brocca, Stefania
Sacco, Elena
Spinelli, Michela
Papaleo, Elena
Lambrughi, Matteo
Alberghina, Lilia
Vanoni, Marco
A comparative study of Whi5 and retinoblastoma proteins: from sequence and structure analysis to intracellular networks
title A comparative study of Whi5 and retinoblastoma proteins: from sequence and structure analysis to intracellular networks
title_full A comparative study of Whi5 and retinoblastoma proteins: from sequence and structure analysis to intracellular networks
title_fullStr A comparative study of Whi5 and retinoblastoma proteins: from sequence and structure analysis to intracellular networks
title_full_unstemmed A comparative study of Whi5 and retinoblastoma proteins: from sequence and structure analysis to intracellular networks
title_short A comparative study of Whi5 and retinoblastoma proteins: from sequence and structure analysis to intracellular networks
title_sort comparative study of whi5 and retinoblastoma proteins: from sequence and structure analysis to intracellular networks
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3897220/
https://www.ncbi.nlm.nih.gov/pubmed/24478706
http://dx.doi.org/10.3389/fphys.2013.00315
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