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The Endoplasmic Reticulum-Mitochondria Encounter Structure Complex Coordinates Coenzyme Q Biosynthesis
Loss of the endoplasmic reticulum (ER)-mitochondria encounter structure (ERMES) complex that resides in contact sites between the yeast ER and mitochondria leads to impaired respiration; however, the reason for that is not clear. We find that in ERMES null mutants, there is an increase in the level...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6441334/ https://www.ncbi.nlm.nih.gov/pubmed/30937424 http://dx.doi.org/10.1177/2515256418825409 |
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author | Eisenberg-Bord, Michal Tsui, Hui S. Antunes, Diana Fernández-del-Río, Lucía Bradley, Michelle C. Dunn, Cory D. Nguyen, Theresa P. T. Rapaport, Doron Clarke, Catherine F. Schuldiner, Maya |
author_facet | Eisenberg-Bord, Michal Tsui, Hui S. Antunes, Diana Fernández-del-Río, Lucía Bradley, Michelle C. Dunn, Cory D. Nguyen, Theresa P. T. Rapaport, Doron Clarke, Catherine F. Schuldiner, Maya |
author_sort | Eisenberg-Bord, Michal |
collection | PubMed |
description | Loss of the endoplasmic reticulum (ER)-mitochondria encounter structure (ERMES) complex that resides in contact sites between the yeast ER and mitochondria leads to impaired respiration; however, the reason for that is not clear. We find that in ERMES null mutants, there is an increase in the level of mRNAs encoding for biosynthetic enzymes of coenzyme Q(6) (CoQ(6)), an essential electron carrier of the mitochondrial respiratory chain. We show that the mega complexes involved in CoQ(6) biosynthesis (CoQ synthomes) are destabilized in ERMES mutants. This, in turn, affects the level and distribution of CoQ(6) within the cell, resulting in reduced mitochondrial CoQ(6). We suggest that these outcomes contribute to the reduced respiration observed in ERMES mutants. Fluorescence microscopy experiments demonstrate close proximity between the CoQ synthome and ERMES, suggesting a spatial coordination. The involvement of the ER-mitochondria contact site in regulation of CoQ(6) biogenesis highlights an additional level of communication between these two organelles. |
format | Online Article Text |
id | pubmed-6441334 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
record_format | MEDLINE/PubMed |
spelling | pubmed-64413342019-03-30 The Endoplasmic Reticulum-Mitochondria Encounter Structure Complex Coordinates Coenzyme Q Biosynthesis Eisenberg-Bord, Michal Tsui, Hui S. Antunes, Diana Fernández-del-Río, Lucía Bradley, Michelle C. Dunn, Cory D. Nguyen, Theresa P. T. Rapaport, Doron Clarke, Catherine F. Schuldiner, Maya Contact (Thousand Oaks) Article Loss of the endoplasmic reticulum (ER)-mitochondria encounter structure (ERMES) complex that resides in contact sites between the yeast ER and mitochondria leads to impaired respiration; however, the reason for that is not clear. We find that in ERMES null mutants, there is an increase in the level of mRNAs encoding for biosynthetic enzymes of coenzyme Q(6) (CoQ(6)), an essential electron carrier of the mitochondrial respiratory chain. We show that the mega complexes involved in CoQ(6) biosynthesis (CoQ synthomes) are destabilized in ERMES mutants. This, in turn, affects the level and distribution of CoQ(6) within the cell, resulting in reduced mitochondrial CoQ(6). We suggest that these outcomes contribute to the reduced respiration observed in ERMES mutants. Fluorescence microscopy experiments demonstrate close proximity between the CoQ synthome and ERMES, suggesting a spatial coordination. The involvement of the ER-mitochondria contact site in regulation of CoQ(6) biogenesis highlights an additional level of communication between these two organelles. 2019-02-22 /pmc/articles/PMC6441334/ /pubmed/30937424 http://dx.doi.org/10.1177/2515256418825409 Text en http://www.creativecommons.org/licenses/by-nc/4.0/ Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Article Eisenberg-Bord, Michal Tsui, Hui S. Antunes, Diana Fernández-del-Río, Lucía Bradley, Michelle C. Dunn, Cory D. Nguyen, Theresa P. T. Rapaport, Doron Clarke, Catherine F. Schuldiner, Maya The Endoplasmic Reticulum-Mitochondria Encounter Structure Complex Coordinates Coenzyme Q Biosynthesis |
title | The Endoplasmic Reticulum-Mitochondria Encounter Structure Complex Coordinates Coenzyme Q Biosynthesis |
title_full | The Endoplasmic Reticulum-Mitochondria Encounter Structure Complex Coordinates Coenzyme Q Biosynthesis |
title_fullStr | The Endoplasmic Reticulum-Mitochondria Encounter Structure Complex Coordinates Coenzyme Q Biosynthesis |
title_full_unstemmed | The Endoplasmic Reticulum-Mitochondria Encounter Structure Complex Coordinates Coenzyme Q Biosynthesis |
title_short | The Endoplasmic Reticulum-Mitochondria Encounter Structure Complex Coordinates Coenzyme Q Biosynthesis |
title_sort | endoplasmic reticulum-mitochondria encounter structure complex coordinates coenzyme q biosynthesis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6441334/ https://www.ncbi.nlm.nih.gov/pubmed/30937424 http://dx.doi.org/10.1177/2515256418825409 |
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