Cargando…
ER-mitochondria contacts promote mtDNA nucleoids active transportation via mitochondrial dynamic tubulation
A human cell contains hundreds to thousands of mitochondrial DNA (mtDNA) packaged into nucleoids. Currently, the segregation and allocation of nucleoids are thought to be passively determined by mitochondrial fusion and division. Here we provide evidence, using live-cell super-resolution imaging, th...
Autores principales: | , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7478960/ https://www.ncbi.nlm.nih.gov/pubmed/32901010 http://dx.doi.org/10.1038/s41467-020-18202-4 |
_version_ | 1783580166907232256 |
---|---|
author | Qin, Jinshan Guo, Yuting Xue, Boxin Shi, Peng Chen, Yang Su, Qian Peter Hao, Huiwen Zhao, Shujuan Wu, Congying Yu, Li Li, Dong Sun, Yujie |
author_facet | Qin, Jinshan Guo, Yuting Xue, Boxin Shi, Peng Chen, Yang Su, Qian Peter Hao, Huiwen Zhao, Shujuan Wu, Congying Yu, Li Li, Dong Sun, Yujie |
author_sort | Qin, Jinshan |
collection | PubMed |
description | A human cell contains hundreds to thousands of mitochondrial DNA (mtDNA) packaged into nucleoids. Currently, the segregation and allocation of nucleoids are thought to be passively determined by mitochondrial fusion and division. Here we provide evidence, using live-cell super-resolution imaging, that nucleoids can be actively transported via KIF5B-driven mitochondrial dynamic tubulation (MDT) activities that predominantly occur at the ER-mitochondria contact sites (EMCS). We further demonstrate that a mitochondrial inner membrane protein complex MICOS links nucleoids to Miro1, a KIF5B receptor on mitochondria, at the EMCS. We show that such active transportation is a mechanism essential for the proper distribution of nucleoids in the peripheral zone of the cell. Together, our work identifies an active transportation mechanism of nucleoids, with EMCS serving as a key platform for the interplay of nucleoids, MICOS, Miro1, and KIF5B to coordinate nucleoids segregation and transportation. |
format | Online Article Text |
id | pubmed-7478960 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-74789602020-09-21 ER-mitochondria contacts promote mtDNA nucleoids active transportation via mitochondrial dynamic tubulation Qin, Jinshan Guo, Yuting Xue, Boxin Shi, Peng Chen, Yang Su, Qian Peter Hao, Huiwen Zhao, Shujuan Wu, Congying Yu, Li Li, Dong Sun, Yujie Nat Commun Article A human cell contains hundreds to thousands of mitochondrial DNA (mtDNA) packaged into nucleoids. Currently, the segregation and allocation of nucleoids are thought to be passively determined by mitochondrial fusion and division. Here we provide evidence, using live-cell super-resolution imaging, that nucleoids can be actively transported via KIF5B-driven mitochondrial dynamic tubulation (MDT) activities that predominantly occur at the ER-mitochondria contact sites (EMCS). We further demonstrate that a mitochondrial inner membrane protein complex MICOS links nucleoids to Miro1, a KIF5B receptor on mitochondria, at the EMCS. We show that such active transportation is a mechanism essential for the proper distribution of nucleoids in the peripheral zone of the cell. Together, our work identifies an active transportation mechanism of nucleoids, with EMCS serving as a key platform for the interplay of nucleoids, MICOS, Miro1, and KIF5B to coordinate nucleoids segregation and transportation. Nature Publishing Group UK 2020-09-08 /pmc/articles/PMC7478960/ /pubmed/32901010 http://dx.doi.org/10.1038/s41467-020-18202-4 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Qin, Jinshan Guo, Yuting Xue, Boxin Shi, Peng Chen, Yang Su, Qian Peter Hao, Huiwen Zhao, Shujuan Wu, Congying Yu, Li Li, Dong Sun, Yujie ER-mitochondria contacts promote mtDNA nucleoids active transportation via mitochondrial dynamic tubulation |
title | ER-mitochondria contacts promote mtDNA nucleoids active transportation via mitochondrial dynamic tubulation |
title_full | ER-mitochondria contacts promote mtDNA nucleoids active transportation via mitochondrial dynamic tubulation |
title_fullStr | ER-mitochondria contacts promote mtDNA nucleoids active transportation via mitochondrial dynamic tubulation |
title_full_unstemmed | ER-mitochondria contacts promote mtDNA nucleoids active transportation via mitochondrial dynamic tubulation |
title_short | ER-mitochondria contacts promote mtDNA nucleoids active transportation via mitochondrial dynamic tubulation |
title_sort | er-mitochondria contacts promote mtdna nucleoids active transportation via mitochondrial dynamic tubulation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7478960/ https://www.ncbi.nlm.nih.gov/pubmed/32901010 http://dx.doi.org/10.1038/s41467-020-18202-4 |
work_keys_str_mv | AT qinjinshan ermitochondriacontactspromotemtdnanucleoidsactivetransportationviamitochondrialdynamictubulation AT guoyuting ermitochondriacontactspromotemtdnanucleoidsactivetransportationviamitochondrialdynamictubulation AT xueboxin ermitochondriacontactspromotemtdnanucleoidsactivetransportationviamitochondrialdynamictubulation AT shipeng ermitochondriacontactspromotemtdnanucleoidsactivetransportationviamitochondrialdynamictubulation AT chenyang ermitochondriacontactspromotemtdnanucleoidsactivetransportationviamitochondrialdynamictubulation AT suqianpeter ermitochondriacontactspromotemtdnanucleoidsactivetransportationviamitochondrialdynamictubulation AT haohuiwen ermitochondriacontactspromotemtdnanucleoidsactivetransportationviamitochondrialdynamictubulation AT zhaoshujuan ermitochondriacontactspromotemtdnanucleoidsactivetransportationviamitochondrialdynamictubulation AT wucongying ermitochondriacontactspromotemtdnanucleoidsactivetransportationviamitochondrialdynamictubulation AT yuli ermitochondriacontactspromotemtdnanucleoidsactivetransportationviamitochondrialdynamictubulation AT lidong ermitochondriacontactspromotemtdnanucleoidsactivetransportationviamitochondrialdynamictubulation AT sunyujie ermitochondriacontactspromotemtdnanucleoidsactivetransportationviamitochondrialdynamictubulation |