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A conserved mechanism for mitochondria-dependent dynein anchoring
Mitochondrial anchors have functions that extend beyond simply positioning mitochondria. In budding yeast, mitochondria drive the assembly of the mitochondrial anchor protein Num1 into clusters, which serve to anchor mitochondria as well as dynein to the cell cortex. Here, we explore a conserved rol...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The American Society for Cell Biology
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6589697/ https://www.ncbi.nlm.nih.gov/pubmed/30649994 http://dx.doi.org/10.1091/mbc.E18-07-0466 |
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author | Kraft, Lauren M. Lackner, Laura L. |
author_facet | Kraft, Lauren M. Lackner, Laura L. |
author_sort | Kraft, Lauren M. |
collection | PubMed |
description | Mitochondrial anchors have functions that extend beyond simply positioning mitochondria. In budding yeast, mitochondria drive the assembly of the mitochondrial anchor protein Num1 into clusters, which serve to anchor mitochondria as well as dynein to the cell cortex. Here, we explore a conserved role for mitochondria in dynein anchoring by examining the tethering functions of the evolutionarily distant Schizosaccharomyces pombe Num1 homologue. In addition to its function in dynein anchoring, we find that S. pombe Num1, also known as Mcp5, interacts with and tethers mitochondria to the plasma membrane in S. pombe and Saccharomyces cerevisiae. Thus, the mitochondria and plasma membrane-binding domains of the Num1 homologues, as well as the membrane features these domains recognize, are conserved. In S. pombe, we find that mitochondria impact the assembly and cellular distribution of Num1 clusters and that Num1 clusters actively engaged in mitochondrial tethering serve as cortical attachment sites for dynein. Thus, mitochondria play a critical and conserved role in the formation and distribution of dynein-anchoring sites at the cell cortex and, as a consequence, impact dynein function. These findings shed light on an ancient mechanism of mitochondria-dependent dynein anchoring that is conserved over more than 450 million years of evolution, raising the intriguing possibility that the role mitochondria play in dynein anchoring and function extends beyond yeast to higher eukaryotes. |
format | Online Article Text |
id | pubmed-6589697 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | The American Society for Cell Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-65896972019-07-10 A conserved mechanism for mitochondria-dependent dynein anchoring Kraft, Lauren M. Lackner, Laura L. Mol Biol Cell Articles Mitochondrial anchors have functions that extend beyond simply positioning mitochondria. In budding yeast, mitochondria drive the assembly of the mitochondrial anchor protein Num1 into clusters, which serve to anchor mitochondria as well as dynein to the cell cortex. Here, we explore a conserved role for mitochondria in dynein anchoring by examining the tethering functions of the evolutionarily distant Schizosaccharomyces pombe Num1 homologue. In addition to its function in dynein anchoring, we find that S. pombe Num1, also known as Mcp5, interacts with and tethers mitochondria to the plasma membrane in S. pombe and Saccharomyces cerevisiae. Thus, the mitochondria and plasma membrane-binding domains of the Num1 homologues, as well as the membrane features these domains recognize, are conserved. In S. pombe, we find that mitochondria impact the assembly and cellular distribution of Num1 clusters and that Num1 clusters actively engaged in mitochondrial tethering serve as cortical attachment sites for dynein. Thus, mitochondria play a critical and conserved role in the formation and distribution of dynein-anchoring sites at the cell cortex and, as a consequence, impact dynein function. These findings shed light on an ancient mechanism of mitochondria-dependent dynein anchoring that is conserved over more than 450 million years of evolution, raising the intriguing possibility that the role mitochondria play in dynein anchoring and function extends beyond yeast to higher eukaryotes. The American Society for Cell Biology 2019-03-01 /pmc/articles/PMC6589697/ /pubmed/30649994 http://dx.doi.org/10.1091/mbc.E18-07-0466 Text en © 2019 Kraft and Lackner. “ASCB®,” “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society for Cell Biology. http://creativecommons.org/licenses/by-nc-sa/3.0 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 3.0 Unported Creative Commons License. |
spellingShingle | Articles Kraft, Lauren M. Lackner, Laura L. A conserved mechanism for mitochondria-dependent dynein anchoring |
title | A conserved mechanism for mitochondria-dependent dynein anchoring |
title_full | A conserved mechanism for mitochondria-dependent dynein anchoring |
title_fullStr | A conserved mechanism for mitochondria-dependent dynein anchoring |
title_full_unstemmed | A conserved mechanism for mitochondria-dependent dynein anchoring |
title_short | A conserved mechanism for mitochondria-dependent dynein anchoring |
title_sort | conserved mechanism for mitochondria-dependent dynein anchoring |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6589697/ https://www.ncbi.nlm.nih.gov/pubmed/30649994 http://dx.doi.org/10.1091/mbc.E18-07-0466 |
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