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Punctuated evolution and transitional hybrid network in an ancestral cell cycle of fungi

Although cell cycle control is an ancient, conserved, and essential process, some core animal and fungal cell cycle regulators share no more sequence identity than non-homologous proteins. Here, we show that evolution along the fungal lineage was punctuated by the early acquisition and entrainment o...

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Autores principales: Medina, Edgar M, Turner, Jonathan J, Gordân, Raluca, Skotheim, Jan M, Buchler, Nicolas E
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4862756/
https://www.ncbi.nlm.nih.gov/pubmed/27162172
http://dx.doi.org/10.7554/eLife.09492
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author Medina, Edgar M
Turner, Jonathan J
Gordân, Raluca
Skotheim, Jan M
Buchler, Nicolas E
author_facet Medina, Edgar M
Turner, Jonathan J
Gordân, Raluca
Skotheim, Jan M
Buchler, Nicolas E
author_sort Medina, Edgar M
collection PubMed
description Although cell cycle control is an ancient, conserved, and essential process, some core animal and fungal cell cycle regulators share no more sequence identity than non-homologous proteins. Here, we show that evolution along the fungal lineage was punctuated by the early acquisition and entrainment of the SBF transcription factor through horizontal gene transfer. Cell cycle evolution in the fungal ancestor then proceeded through a hybrid network containing both SBF and its ancestral animal counterpart E2F, which is still maintained in many basal fungi. We hypothesize that a virally-derived SBF may have initially hijacked cell cycle control by activating transcription via the cis-regulatory elements targeted by the ancestral cell cycle regulator E2F, much like extant viral oncogenes. Consistent with this hypothesis, we show that SBF can regulate promoters with E2F binding sites in budding yeast. DOI: http://dx.doi.org/10.7554/eLife.09492.001
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spelling pubmed-48627562016-05-11 Punctuated evolution and transitional hybrid network in an ancestral cell cycle of fungi Medina, Edgar M Turner, Jonathan J Gordân, Raluca Skotheim, Jan M Buchler, Nicolas E eLife Computational and Systems Biology Although cell cycle control is an ancient, conserved, and essential process, some core animal and fungal cell cycle regulators share no more sequence identity than non-homologous proteins. Here, we show that evolution along the fungal lineage was punctuated by the early acquisition and entrainment of the SBF transcription factor through horizontal gene transfer. Cell cycle evolution in the fungal ancestor then proceeded through a hybrid network containing both SBF and its ancestral animal counterpart E2F, which is still maintained in many basal fungi. We hypothesize that a virally-derived SBF may have initially hijacked cell cycle control by activating transcription via the cis-regulatory elements targeted by the ancestral cell cycle regulator E2F, much like extant viral oncogenes. Consistent with this hypothesis, we show that SBF can regulate promoters with E2F binding sites in budding yeast. DOI: http://dx.doi.org/10.7554/eLife.09492.001 eLife Sciences Publications, Ltd 2016-05-10 /pmc/articles/PMC4862756/ /pubmed/27162172 http://dx.doi.org/10.7554/eLife.09492 Text en © 2016, Medina et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Computational and Systems Biology
Medina, Edgar M
Turner, Jonathan J
Gordân, Raluca
Skotheim, Jan M
Buchler, Nicolas E
Punctuated evolution and transitional hybrid network in an ancestral cell cycle of fungi
title Punctuated evolution and transitional hybrid network in an ancestral cell cycle of fungi
title_full Punctuated evolution and transitional hybrid network in an ancestral cell cycle of fungi
title_fullStr Punctuated evolution and transitional hybrid network in an ancestral cell cycle of fungi
title_full_unstemmed Punctuated evolution and transitional hybrid network in an ancestral cell cycle of fungi
title_short Punctuated evolution and transitional hybrid network in an ancestral cell cycle of fungi
title_sort punctuated evolution and transitional hybrid network in an ancestral cell cycle of fungi
topic Computational and Systems Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4862756/
https://www.ncbi.nlm.nih.gov/pubmed/27162172
http://dx.doi.org/10.7554/eLife.09492
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