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Hierarchical integration of mitochondrial and nuclear positioning pathways by the Num1 EF hand
Positioning organelles at the right place and time is critical for their function and inheritance. In budding yeast, mitochondrial and nuclear positioning require the anchoring of mitochondria and dynein to the cell cortex by clusters of Num1. We have previously shown that mitochondria drive the ass...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The American Society for Cell Biology
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9236139/ https://www.ncbi.nlm.nih.gov/pubmed/34985939 http://dx.doi.org/10.1091/mbc.E21-12-0610-T |
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author | Anderson, Heidi L. Casler, Jason C. Lackner, Laura L. |
author_facet | Anderson, Heidi L. Casler, Jason C. Lackner, Laura L. |
author_sort | Anderson, Heidi L. |
collection | PubMed |
description | Positioning organelles at the right place and time is critical for their function and inheritance. In budding yeast, mitochondrial and nuclear positioning require the anchoring of mitochondria and dynein to the cell cortex by clusters of Num1. We have previously shown that mitochondria drive the assembly of cortical Num1 clusters, which then serve as anchoring sites for mitochondria and dynein. When mitochondrial inheritance is inhibited, mitochondrial-driven assembly of Num1 in buds is disrupted and defects in dynein-mediated spindle positioning are observed. Using a structure-function approach to dissect the mechanism of mitochondria-dependent dynein anchoring, we found that the EF hand–like motif (EFLM) of Num1 and its ability to bind calcium are required to bias dynein anchoring on mitochondria-associated Num1 clusters. Consistently, when the EFLM is disrupted, we no longer observe defects in dynein activity following inhibition of mitochondrial inheritance. Thus, the Num1 EFLM functions to bias dynein anchoring and activity in nuclear inheritance subsequent to mitochondrial inheritance. We hypothesize that this hierarchical integration of organelle positioning pathways by the Num1 EFLM contributes to the regulated order of organelle inheritance during the cell cycle. |
format | Online Article Text |
id | pubmed-9236139 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The American Society for Cell Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-92361392022-06-28 Hierarchical integration of mitochondrial and nuclear positioning pathways by the Num1 EF hand Anderson, Heidi L. Casler, Jason C. Lackner, Laura L. Mol Biol Cell Articles Positioning organelles at the right place and time is critical for their function and inheritance. In budding yeast, mitochondrial and nuclear positioning require the anchoring of mitochondria and dynein to the cell cortex by clusters of Num1. We have previously shown that mitochondria drive the assembly of cortical Num1 clusters, which then serve as anchoring sites for mitochondria and dynein. When mitochondrial inheritance is inhibited, mitochondrial-driven assembly of Num1 in buds is disrupted and defects in dynein-mediated spindle positioning are observed. Using a structure-function approach to dissect the mechanism of mitochondria-dependent dynein anchoring, we found that the EF hand–like motif (EFLM) of Num1 and its ability to bind calcium are required to bias dynein anchoring on mitochondria-associated Num1 clusters. Consistently, when the EFLM is disrupted, we no longer observe defects in dynein activity following inhibition of mitochondrial inheritance. Thus, the Num1 EFLM functions to bias dynein anchoring and activity in nuclear inheritance subsequent to mitochondrial inheritance. We hypothesize that this hierarchical integration of organelle positioning pathways by the Num1 EFLM contributes to the regulated order of organelle inheritance during the cell cycle. The American Society for Cell Biology 2022-01-27 /pmc/articles/PMC9236139/ /pubmed/34985939 http://dx.doi.org/10.1091/mbc.E21-12-0610-T Text en © 2022 Anderson et al. “ASCB®,” “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society for Cell Biology. https://creativecommons.org/licenses/by-nc-sa/4.0/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 4.0 International Creative Commons License. |
spellingShingle | Articles Anderson, Heidi L. Casler, Jason C. Lackner, Laura L. Hierarchical integration of mitochondrial and nuclear positioning pathways by the Num1 EF hand |
title | Hierarchical integration of mitochondrial and nuclear positioning pathways by the Num1 EF hand |
title_full | Hierarchical integration of mitochondrial and nuclear positioning pathways by the Num1 EF hand |
title_fullStr | Hierarchical integration of mitochondrial and nuclear positioning pathways by the Num1 EF hand |
title_full_unstemmed | Hierarchical integration of mitochondrial and nuclear positioning pathways by the Num1 EF hand |
title_short | Hierarchical integration of mitochondrial and nuclear positioning pathways by the Num1 EF hand |
title_sort | hierarchical integration of mitochondrial and nuclear positioning pathways by the num1 ef hand |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9236139/ https://www.ncbi.nlm.nih.gov/pubmed/34985939 http://dx.doi.org/10.1091/mbc.E21-12-0610-T |
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