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Tim29 is a novel subunit of the human TIM22 translocase and is involved in complex assembly and stability
The TIM22 complex mediates the import of hydrophobic carrier proteins into the mitochondrial inner membrane. While the TIM22 machinery has been well characterised in yeast, the human complex remains poorly characterised. Here, we identify Tim29 (C19orf52) as a novel, metazoan-specific subunit of the...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5016092/ https://www.ncbi.nlm.nih.gov/pubmed/27554484 http://dx.doi.org/10.7554/eLife.17463 |
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author | Kang, Yilin Baker, Michael James Liem, Michael Louber, Jade McKenzie, Matthew Atukorala, Ishara Ang, Ching-Seng Keerthikumar, Shivakumar Mathivanan, Suresh Stojanovski, Diana |
author_facet | Kang, Yilin Baker, Michael James Liem, Michael Louber, Jade McKenzie, Matthew Atukorala, Ishara Ang, Ching-Seng Keerthikumar, Shivakumar Mathivanan, Suresh Stojanovski, Diana |
author_sort | Kang, Yilin |
collection | PubMed |
description | The TIM22 complex mediates the import of hydrophobic carrier proteins into the mitochondrial inner membrane. While the TIM22 machinery has been well characterised in yeast, the human complex remains poorly characterised. Here, we identify Tim29 (C19orf52) as a novel, metazoan-specific subunit of the human TIM22 complex. The protein is integrated into the mitochondrial inner membrane with it’s C-terminus exposed to the intermembrane space. Tim29 is required for the stability of the TIM22 complex and functions in the assembly of hTim22. Furthermore, Tim29 contacts the Translocase of the Outer Mitochondrial Membrane, TOM complex, enabling a mechanism for transport of hydrophobic carrier substrates across the aqueous intermembrane space. Identification of Tim29 highlights the significance of analysing mitochondrial import systems across phylogenetic boundaries, which can reveal novel components and mechanisms in higher organisms. DOI: http://dx.doi.org/10.7554/eLife.17463.001 |
format | Online Article Text |
id | pubmed-5016092 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-50160922016-09-09 Tim29 is a novel subunit of the human TIM22 translocase and is involved in complex assembly and stability Kang, Yilin Baker, Michael James Liem, Michael Louber, Jade McKenzie, Matthew Atukorala, Ishara Ang, Ching-Seng Keerthikumar, Shivakumar Mathivanan, Suresh Stojanovski, Diana eLife Biochemistry The TIM22 complex mediates the import of hydrophobic carrier proteins into the mitochondrial inner membrane. While the TIM22 machinery has been well characterised in yeast, the human complex remains poorly characterised. Here, we identify Tim29 (C19orf52) as a novel, metazoan-specific subunit of the human TIM22 complex. The protein is integrated into the mitochondrial inner membrane with it’s C-terminus exposed to the intermembrane space. Tim29 is required for the stability of the TIM22 complex and functions in the assembly of hTim22. Furthermore, Tim29 contacts the Translocase of the Outer Mitochondrial Membrane, TOM complex, enabling a mechanism for transport of hydrophobic carrier substrates across the aqueous intermembrane space. Identification of Tim29 highlights the significance of analysing mitochondrial import systems across phylogenetic boundaries, which can reveal novel components and mechanisms in higher organisms. DOI: http://dx.doi.org/10.7554/eLife.17463.001 eLife Sciences Publications, Ltd 2016-08-24 /pmc/articles/PMC5016092/ /pubmed/27554484 http://dx.doi.org/10.7554/eLife.17463 Text en © 2016, Kang et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Biochemistry Kang, Yilin Baker, Michael James Liem, Michael Louber, Jade McKenzie, Matthew Atukorala, Ishara Ang, Ching-Seng Keerthikumar, Shivakumar Mathivanan, Suresh Stojanovski, Diana Tim29 is a novel subunit of the human TIM22 translocase and is involved in complex assembly and stability |
title | Tim29 is a novel subunit of the human TIM22 translocase and is involved in complex assembly and stability |
title_full | Tim29 is a novel subunit of the human TIM22 translocase and is involved in complex assembly and stability |
title_fullStr | Tim29 is a novel subunit of the human TIM22 translocase and is involved in complex assembly and stability |
title_full_unstemmed | Tim29 is a novel subunit of the human TIM22 translocase and is involved in complex assembly and stability |
title_short | Tim29 is a novel subunit of the human TIM22 translocase and is involved in complex assembly and stability |
title_sort | tim29 is a novel subunit of the human tim22 translocase and is involved in complex assembly and stability |
topic | Biochemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5016092/ https://www.ncbi.nlm.nih.gov/pubmed/27554484 http://dx.doi.org/10.7554/eLife.17463 |
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