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Mitotic regulation of fungal cell-to-cell connectivity through septal pores involves the NIMA kinase
Intercellular bridges are a conserved feature of multicellular organisms. In multicellular fungi, cells are connected directly via intercellular bridges called septal pores. Using Aspergillus nidulans, we demonstrate for the first time that septal pores are regulated to be opened during interphase b...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The American Society for Cell Biology
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3952847/ https://www.ncbi.nlm.nih.gov/pubmed/24451264 http://dx.doi.org/10.1091/mbc.E13-12-0718 |
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author | Shen, Kuo-Fang Osmani, Aysha H. Govindaraghavan, Meera Osmani, Stephen A. |
author_facet | Shen, Kuo-Fang Osmani, Aysha H. Govindaraghavan, Meera Osmani, Stephen A. |
author_sort | Shen, Kuo-Fang |
collection | PubMed |
description | Intercellular bridges are a conserved feature of multicellular organisms. In multicellular fungi, cells are connected directly via intercellular bridges called septal pores. Using Aspergillus nidulans, we demonstrate for the first time that septal pores are regulated to be opened during interphase but closed during mitosis. Septal pore–associated proteins display dynamic cell cycle–regulated locations at mature septa. Of importance, the mitotic NIMA kinase locates to forming septa and surprisingly then remains at septa throughout interphase. However, during mitosis, when NIMA transiently locates to nuclei to promote mitosis, its levels at septa drop. A model is proposed in which NIMA helps keep septal pores open during interphase and then closed when it is removed from them during mitosis. In support of this hypothesis, NIMA inactivation is shown to promote interphase septal pore closing. Because NIMA triggers nuclear pore complex opening during mitosis, our findings suggest that common cell cycle regulatory mechanisms might control septal pores and nuclear pores such that they are opened and closed out of phase to each other during cell cycle progression. The study provides insights into how and why cytoplasmically connected Aspergillus cells maintain mitotic autonomy. |
format | Online Article Text |
id | pubmed-3952847 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | The American Society for Cell Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-39528472014-05-30 Mitotic regulation of fungal cell-to-cell connectivity through septal pores involves the NIMA kinase Shen, Kuo-Fang Osmani, Aysha H. Govindaraghavan, Meera Osmani, Stephen A. Mol Biol Cell Articles Intercellular bridges are a conserved feature of multicellular organisms. In multicellular fungi, cells are connected directly via intercellular bridges called septal pores. Using Aspergillus nidulans, we demonstrate for the first time that septal pores are regulated to be opened during interphase but closed during mitosis. Septal pore–associated proteins display dynamic cell cycle–regulated locations at mature septa. Of importance, the mitotic NIMA kinase locates to forming septa and surprisingly then remains at septa throughout interphase. However, during mitosis, when NIMA transiently locates to nuclei to promote mitosis, its levels at septa drop. A model is proposed in which NIMA helps keep septal pores open during interphase and then closed when it is removed from them during mitosis. In support of this hypothesis, NIMA inactivation is shown to promote interphase septal pore closing. Because NIMA triggers nuclear pore complex opening during mitosis, our findings suggest that common cell cycle regulatory mechanisms might control septal pores and nuclear pores such that they are opened and closed out of phase to each other during cell cycle progression. The study provides insights into how and why cytoplasmically connected Aspergillus cells maintain mitotic autonomy. The American Society for Cell Biology 2014-03-15 /pmc/articles/PMC3952847/ /pubmed/24451264 http://dx.doi.org/10.1091/mbc.E13-12-0718 Text en © 2014 Shen et al. This article is distributed by The American Society for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial–Share Alike 3.0 Unported Creative Commons License (http://creativecommons.org/licenses/by-nc-sa/3.0). “ASCB®,” “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society of Cell Biology. |
spellingShingle | Articles Shen, Kuo-Fang Osmani, Aysha H. Govindaraghavan, Meera Osmani, Stephen A. Mitotic regulation of fungal cell-to-cell connectivity through septal pores involves the NIMA kinase |
title | Mitotic regulation of fungal cell-to-cell connectivity through septal pores involves the NIMA kinase |
title_full | Mitotic regulation of fungal cell-to-cell connectivity through septal pores involves the NIMA kinase |
title_fullStr | Mitotic regulation of fungal cell-to-cell connectivity through septal pores involves the NIMA kinase |
title_full_unstemmed | Mitotic regulation of fungal cell-to-cell connectivity through septal pores involves the NIMA kinase |
title_short | Mitotic regulation of fungal cell-to-cell connectivity through septal pores involves the NIMA kinase |
title_sort | mitotic regulation of fungal cell-to-cell connectivity through septal pores involves the nima kinase |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3952847/ https://www.ncbi.nlm.nih.gov/pubmed/24451264 http://dx.doi.org/10.1091/mbc.E13-12-0718 |
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