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Patronus is the elusive plant securin, preventing chromosome separation by antagonizing separase

Chromosome distribution at anaphase of mitosis and meiosis is triggered by separase, an evolutionarily conserved protease. Separase must be tightly regulated to prevent the untimely release of chromatid cohesion and disastrous chromosome distribution defects. Securin is the key inhibitor of separase...

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Autores principales: Cromer, Laurence, Jolivet, Sylvie, Singh, Dipesh Kumar, Berthier, Floriane, De Winne, Nancy, De Jaeger, Geert, Komaki, Shinichiro, Prusicki, Maria Ada, Schnittger, Arp, Guérois, Raphael, Mercier, Raphael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6690013/
https://www.ncbi.nlm.nih.gov/pubmed/31324745
http://dx.doi.org/10.1073/pnas.1906237116
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author Cromer, Laurence
Jolivet, Sylvie
Singh, Dipesh Kumar
Berthier, Floriane
De Winne, Nancy
De Jaeger, Geert
Komaki, Shinichiro
Prusicki, Maria Ada
Schnittger, Arp
Guérois, Raphael
Mercier, Raphael
author_facet Cromer, Laurence
Jolivet, Sylvie
Singh, Dipesh Kumar
Berthier, Floriane
De Winne, Nancy
De Jaeger, Geert
Komaki, Shinichiro
Prusicki, Maria Ada
Schnittger, Arp
Guérois, Raphael
Mercier, Raphael
author_sort Cromer, Laurence
collection PubMed
description Chromosome distribution at anaphase of mitosis and meiosis is triggered by separase, an evolutionarily conserved protease. Separase must be tightly regulated to prevent the untimely release of chromatid cohesion and disastrous chromosome distribution defects. Securin is the key inhibitor of separase in animals and fungi, but has not been identified in other eukaryotic lineages. Here, we identified PATRONUS1 and PATRONUS2 (PANS1 and PANS2) as the Arabidopsis homologs of securin. Disruption of PANS1 is known to lead to the premature separation of chromosomes at meiosis, and the simultaneous disruption of PANS1 and PANS2 is lethal. Here, we show that PANS1 targeting by the anaphase-promoting complex is required to trigger chromosome separation, mirroring the regulation of securin. We showed that PANS1 acts independently from Shugosins. In a genetic screen for pans1 suppressors, we identified SEPARASE mutants, showing that PANS1 and SEPARASE have antagonistic functions in vivo. Finally, we showed that the PANS1 and PANS2 proteins interact directly with SEPARASE. Altogether, our results show that PANS1 and PANS2 act as a plant securin. Remote sequence similarity was identified between the plant patronus family and animal securins, suggesting that they indeed derive from a common ancestor. Identification of patronus as the elusive plant securin illustrates the extreme sequence divergence of this central regulator of mitosis and meiosis.
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spelling pubmed-66900132019-08-14 Patronus is the elusive plant securin, preventing chromosome separation by antagonizing separase Cromer, Laurence Jolivet, Sylvie Singh, Dipesh Kumar Berthier, Floriane De Winne, Nancy De Jaeger, Geert Komaki, Shinichiro Prusicki, Maria Ada Schnittger, Arp Guérois, Raphael Mercier, Raphael Proc Natl Acad Sci U S A PNAS Plus Chromosome distribution at anaphase of mitosis and meiosis is triggered by separase, an evolutionarily conserved protease. Separase must be tightly regulated to prevent the untimely release of chromatid cohesion and disastrous chromosome distribution defects. Securin is the key inhibitor of separase in animals and fungi, but has not been identified in other eukaryotic lineages. Here, we identified PATRONUS1 and PATRONUS2 (PANS1 and PANS2) as the Arabidopsis homologs of securin. Disruption of PANS1 is known to lead to the premature separation of chromosomes at meiosis, and the simultaneous disruption of PANS1 and PANS2 is lethal. Here, we show that PANS1 targeting by the anaphase-promoting complex is required to trigger chromosome separation, mirroring the regulation of securin. We showed that PANS1 acts independently from Shugosins. In a genetic screen for pans1 suppressors, we identified SEPARASE mutants, showing that PANS1 and SEPARASE have antagonistic functions in vivo. Finally, we showed that the PANS1 and PANS2 proteins interact directly with SEPARASE. Altogether, our results show that PANS1 and PANS2 act as a plant securin. Remote sequence similarity was identified between the plant patronus family and animal securins, suggesting that they indeed derive from a common ancestor. Identification of patronus as the elusive plant securin illustrates the extreme sequence divergence of this central regulator of mitosis and meiosis. National Academy of Sciences 2019-08-06 2019-07-19 /pmc/articles/PMC6690013/ /pubmed/31324745 http://dx.doi.org/10.1073/pnas.1906237116 Text en Copyright © 2019 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/ https://creativecommons.org/licenses/by-nc-nd/4.0/This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle PNAS Plus
Cromer, Laurence
Jolivet, Sylvie
Singh, Dipesh Kumar
Berthier, Floriane
De Winne, Nancy
De Jaeger, Geert
Komaki, Shinichiro
Prusicki, Maria Ada
Schnittger, Arp
Guérois, Raphael
Mercier, Raphael
Patronus is the elusive plant securin, preventing chromosome separation by antagonizing separase
title Patronus is the elusive plant securin, preventing chromosome separation by antagonizing separase
title_full Patronus is the elusive plant securin, preventing chromosome separation by antagonizing separase
title_fullStr Patronus is the elusive plant securin, preventing chromosome separation by antagonizing separase
title_full_unstemmed Patronus is the elusive plant securin, preventing chromosome separation by antagonizing separase
title_short Patronus is the elusive plant securin, preventing chromosome separation by antagonizing separase
title_sort patronus is the elusive plant securin, preventing chromosome separation by antagonizing separase
topic PNAS Plus
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6690013/
https://www.ncbi.nlm.nih.gov/pubmed/31324745
http://dx.doi.org/10.1073/pnas.1906237116
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