Cargando…

Detailed Analysis of the Human Mitochondrial Contact Site Complex Indicate a Hierarchy of Subunits

Mitochondrial inner membrane folds into cristae, which significantly increase its surface and are important for mitochondrial function. The stability of cristae depends on the mitochondrial contact site (MICOS) complex. In human mitochondria, the inner membrane MICOS complex interacts with the outer...

Descripción completa

Detalles Bibliográficos
Autores principales: Ott, Christine, Dorsch, Eva, Fraunholz, Martin, Straub, Sebastian, Kozjak-Pavlovic, Vera
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4363703/
https://www.ncbi.nlm.nih.gov/pubmed/25781180
http://dx.doi.org/10.1371/journal.pone.0120213
_version_ 1782361961464332288
author Ott, Christine
Dorsch, Eva
Fraunholz, Martin
Straub, Sebastian
Kozjak-Pavlovic, Vera
author_facet Ott, Christine
Dorsch, Eva
Fraunholz, Martin
Straub, Sebastian
Kozjak-Pavlovic, Vera
author_sort Ott, Christine
collection PubMed
description Mitochondrial inner membrane folds into cristae, which significantly increase its surface and are important for mitochondrial function. The stability of cristae depends on the mitochondrial contact site (MICOS) complex. In human mitochondria, the inner membrane MICOS complex interacts with the outer membrane sorting and assembly machinery (SAM) complex, to form the mitochondrial intermembrane space bridging complex (MIB). We have created knockdown cell lines of most of the MICOS and MIB components and have used them to study the importance of the individual subunits for the cristae formation and complex stability. We show that the most important subunits of the MIB complex in human mitochondria are Mic60/Mitofilin, Mic19/CHCHD3 and an outer membrane component Sam50. We provide additional proof that ApoO indeed is a subunit of the MICOS and MIB complexes and propose the name Mic23 for this protein. According to our results, Mic25/CHCHD6, Mic27/ApoOL and Mic23/ApoO appear to be periphery subunits of the MICOS complex, because their depletion does not affect cristae morphology or stability of other components.
format Online
Article
Text
id pubmed-4363703
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-43637032015-03-23 Detailed Analysis of the Human Mitochondrial Contact Site Complex Indicate a Hierarchy of Subunits Ott, Christine Dorsch, Eva Fraunholz, Martin Straub, Sebastian Kozjak-Pavlovic, Vera PLoS One Research Article Mitochondrial inner membrane folds into cristae, which significantly increase its surface and are important for mitochondrial function. The stability of cristae depends on the mitochondrial contact site (MICOS) complex. In human mitochondria, the inner membrane MICOS complex interacts with the outer membrane sorting and assembly machinery (SAM) complex, to form the mitochondrial intermembrane space bridging complex (MIB). We have created knockdown cell lines of most of the MICOS and MIB components and have used them to study the importance of the individual subunits for the cristae formation and complex stability. We show that the most important subunits of the MIB complex in human mitochondria are Mic60/Mitofilin, Mic19/CHCHD3 and an outer membrane component Sam50. We provide additional proof that ApoO indeed is a subunit of the MICOS and MIB complexes and propose the name Mic23 for this protein. According to our results, Mic25/CHCHD6, Mic27/ApoOL and Mic23/ApoO appear to be periphery subunits of the MICOS complex, because their depletion does not affect cristae morphology or stability of other components. Public Library of Science 2015-03-17 /pmc/articles/PMC4363703/ /pubmed/25781180 http://dx.doi.org/10.1371/journal.pone.0120213 Text en © 2015 Ott et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Ott, Christine
Dorsch, Eva
Fraunholz, Martin
Straub, Sebastian
Kozjak-Pavlovic, Vera
Detailed Analysis of the Human Mitochondrial Contact Site Complex Indicate a Hierarchy of Subunits
title Detailed Analysis of the Human Mitochondrial Contact Site Complex Indicate a Hierarchy of Subunits
title_full Detailed Analysis of the Human Mitochondrial Contact Site Complex Indicate a Hierarchy of Subunits
title_fullStr Detailed Analysis of the Human Mitochondrial Contact Site Complex Indicate a Hierarchy of Subunits
title_full_unstemmed Detailed Analysis of the Human Mitochondrial Contact Site Complex Indicate a Hierarchy of Subunits
title_short Detailed Analysis of the Human Mitochondrial Contact Site Complex Indicate a Hierarchy of Subunits
title_sort detailed analysis of the human mitochondrial contact site complex indicate a hierarchy of subunits
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4363703/
https://www.ncbi.nlm.nih.gov/pubmed/25781180
http://dx.doi.org/10.1371/journal.pone.0120213
work_keys_str_mv AT ottchristine detailedanalysisofthehumanmitochondrialcontactsitecomplexindicateahierarchyofsubunits
AT dorscheva detailedanalysisofthehumanmitochondrialcontactsitecomplexindicateahierarchyofsubunits
AT fraunholzmartin detailedanalysisofthehumanmitochondrialcontactsitecomplexindicateahierarchyofsubunits
AT straubsebastian detailedanalysisofthehumanmitochondrialcontactsitecomplexindicateahierarchyofsubunits
AT kozjakpavlovicvera detailedanalysisofthehumanmitochondrialcontactsitecomplexindicateahierarchyofsubunits