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Genome-Wide Analysis of Cell Cycle-Regulating Genes in the Symbiotic Dinoflagellate Breviolum minutum

A delicate relationship exists between reef-building corals and their photosynthetic endosymbionts. Unfortunately, this relationship can be disrupted, with corals expelling these algae when temperatures rise even marginally above the average summer maximum. Interestingly, several studies indicate th...

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Autores principales: Cato, Michael L., Jester, Hallie D., Lavertu, Adam, Lyman, Audrey, Tallent, Lacey M., Mitchell, Geoffrey C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Genetics Society of America 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6829154/
https://www.ncbi.nlm.nih.gov/pubmed/31551286
http://dx.doi.org/10.1534/g3.119.400363
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author Cato, Michael L.
Jester, Hallie D.
Lavertu, Adam
Lyman, Audrey
Tallent, Lacey M.
Mitchell, Geoffrey C.
author_facet Cato, Michael L.
Jester, Hallie D.
Lavertu, Adam
Lyman, Audrey
Tallent, Lacey M.
Mitchell, Geoffrey C.
author_sort Cato, Michael L.
collection PubMed
description A delicate relationship exists between reef-building corals and their photosynthetic endosymbionts. Unfortunately, this relationship can be disrupted, with corals expelling these algae when temperatures rise even marginally above the average summer maximum. Interestingly, several studies indicate that failure of corals to regulate symbiont cell divisions at high temperatures may underlie this disruption; increased proliferation of symbionts may stress host cells by over-production of reactive oxygen species or by disrupting the flow of nutrients. This needs to be further investigated, so to begin deciphering the molecular mechanisms controlling the cell cycle in these organisms, we used a computational approach to identify putative cell cycle-regulating genes in the genome of the dinoflagellate Breviolum minutum. This species is important as an endosymbiont of Aiptasia pallida—an anemone that is used as a model for studying coral biology. We then correlated expression of these putative cell cycle genes with cell cycle phase in diurnally growing B. minutum in culture. This approach allowed us to identify a cyclin/cyclin-dependent kinase pair that may function in the G1/S transition—a likely point for coral cells to exert control over algal cell divisions.
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spelling pubmed-68291542019-11-06 Genome-Wide Analysis of Cell Cycle-Regulating Genes in the Symbiotic Dinoflagellate Breviolum minutum Cato, Michael L. Jester, Hallie D. Lavertu, Adam Lyman, Audrey Tallent, Lacey M. Mitchell, Geoffrey C. G3 (Bethesda) Investigations A delicate relationship exists between reef-building corals and their photosynthetic endosymbionts. Unfortunately, this relationship can be disrupted, with corals expelling these algae when temperatures rise even marginally above the average summer maximum. Interestingly, several studies indicate that failure of corals to regulate symbiont cell divisions at high temperatures may underlie this disruption; increased proliferation of symbionts may stress host cells by over-production of reactive oxygen species or by disrupting the flow of nutrients. This needs to be further investigated, so to begin deciphering the molecular mechanisms controlling the cell cycle in these organisms, we used a computational approach to identify putative cell cycle-regulating genes in the genome of the dinoflagellate Breviolum minutum. This species is important as an endosymbiont of Aiptasia pallida—an anemone that is used as a model for studying coral biology. We then correlated expression of these putative cell cycle genes with cell cycle phase in diurnally growing B. minutum in culture. This approach allowed us to identify a cyclin/cyclin-dependent kinase pair that may function in the G1/S transition—a likely point for coral cells to exert control over algal cell divisions. Genetics Society of America 2019-09-24 /pmc/articles/PMC6829154/ /pubmed/31551286 http://dx.doi.org/10.1534/g3.119.400363 Text en Copyright © 2019 Cato et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Investigations
Cato, Michael L.
Jester, Hallie D.
Lavertu, Adam
Lyman, Audrey
Tallent, Lacey M.
Mitchell, Geoffrey C.
Genome-Wide Analysis of Cell Cycle-Regulating Genes in the Symbiotic Dinoflagellate Breviolum minutum
title Genome-Wide Analysis of Cell Cycle-Regulating Genes in the Symbiotic Dinoflagellate Breviolum minutum
title_full Genome-Wide Analysis of Cell Cycle-Regulating Genes in the Symbiotic Dinoflagellate Breviolum minutum
title_fullStr Genome-Wide Analysis of Cell Cycle-Regulating Genes in the Symbiotic Dinoflagellate Breviolum minutum
title_full_unstemmed Genome-Wide Analysis of Cell Cycle-Regulating Genes in the Symbiotic Dinoflagellate Breviolum minutum
title_short Genome-Wide Analysis of Cell Cycle-Regulating Genes in the Symbiotic Dinoflagellate Breviolum minutum
title_sort genome-wide analysis of cell cycle-regulating genes in the symbiotic dinoflagellate breviolum minutum
topic Investigations
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6829154/
https://www.ncbi.nlm.nih.gov/pubmed/31551286
http://dx.doi.org/10.1534/g3.119.400363
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