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The mitochondrial inner membrane protein LETM1 modulates cristae organization through its LETM domain
LETM1 is a mitochondrial inner membrane protein that is required for maintaining the mitochondrial morphology and cristae structures, and regulates mitochondrial ion homeostasis. Here we report a role of LETM1 in the organization of cristae structures. We identified four amino acid residues of human...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7058069/ https://www.ncbi.nlm.nih.gov/pubmed/32139798 http://dx.doi.org/10.1038/s42003-020-0832-5 |
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author | Nakamura, Seiko Matsui, Aiko Akabane, Shiori Tamura, Yasushi Hatano, Azumi Miyano, Yuriko Omote, Hiroshi Kajikawa, Mizuho Maenaka, Katsumi Moriyama, Yoshinori Endo, Toshiya Oka, Toshihiko |
author_facet | Nakamura, Seiko Matsui, Aiko Akabane, Shiori Tamura, Yasushi Hatano, Azumi Miyano, Yuriko Omote, Hiroshi Kajikawa, Mizuho Maenaka, Katsumi Moriyama, Yoshinori Endo, Toshiya Oka, Toshihiko |
author_sort | Nakamura, Seiko |
collection | PubMed |
description | LETM1 is a mitochondrial inner membrane protein that is required for maintaining the mitochondrial morphology and cristae structures, and regulates mitochondrial ion homeostasis. Here we report a role of LETM1 in the organization of cristae structures. We identified four amino acid residues of human LETM1 that are crucial for complementation of the growth deficiency caused by gene deletion of a yeast LETM1 orthologue. Substituting amino acid residues with alanine disrupts the correct assembly of a protein complex containing LETM1 and prevents changes in the mitochondrial morphology induced by exogenous LETM1 expression. Moreover, the LETM1 protein changes the shapes of the membranes of in vitro-reconstituted proteoliposomes, leading to the formation of invaginated membrane structures on artificial liposomes. LETM1 mutant proteins with alanine substitutions fail to facilitate the formation of invaginated membrane structures, suggesting that LETM1 plays a fundamental role in the organization of mitochondrial membrane morphology. |
format | Online Article Text |
id | pubmed-7058069 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-70580692020-03-19 The mitochondrial inner membrane protein LETM1 modulates cristae organization through its LETM domain Nakamura, Seiko Matsui, Aiko Akabane, Shiori Tamura, Yasushi Hatano, Azumi Miyano, Yuriko Omote, Hiroshi Kajikawa, Mizuho Maenaka, Katsumi Moriyama, Yoshinori Endo, Toshiya Oka, Toshihiko Commun Biol Article LETM1 is a mitochondrial inner membrane protein that is required for maintaining the mitochondrial morphology and cristae structures, and regulates mitochondrial ion homeostasis. Here we report a role of LETM1 in the organization of cristae structures. We identified four amino acid residues of human LETM1 that are crucial for complementation of the growth deficiency caused by gene deletion of a yeast LETM1 orthologue. Substituting amino acid residues with alanine disrupts the correct assembly of a protein complex containing LETM1 and prevents changes in the mitochondrial morphology induced by exogenous LETM1 expression. Moreover, the LETM1 protein changes the shapes of the membranes of in vitro-reconstituted proteoliposomes, leading to the formation of invaginated membrane structures on artificial liposomes. LETM1 mutant proteins with alanine substitutions fail to facilitate the formation of invaginated membrane structures, suggesting that LETM1 plays a fundamental role in the organization of mitochondrial membrane morphology. Nature Publishing Group UK 2020-03-05 /pmc/articles/PMC7058069/ /pubmed/32139798 http://dx.doi.org/10.1038/s42003-020-0832-5 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 Nakamura, Seiko Matsui, Aiko Akabane, Shiori Tamura, Yasushi Hatano, Azumi Miyano, Yuriko Omote, Hiroshi Kajikawa, Mizuho Maenaka, Katsumi Moriyama, Yoshinori Endo, Toshiya Oka, Toshihiko The mitochondrial inner membrane protein LETM1 modulates cristae organization through its LETM domain |
title | The mitochondrial inner membrane protein LETM1 modulates cristae organization through its LETM domain |
title_full | The mitochondrial inner membrane protein LETM1 modulates cristae organization through its LETM domain |
title_fullStr | The mitochondrial inner membrane protein LETM1 modulates cristae organization through its LETM domain |
title_full_unstemmed | The mitochondrial inner membrane protein LETM1 modulates cristae organization through its LETM domain |
title_short | The mitochondrial inner membrane protein LETM1 modulates cristae organization through its LETM domain |
title_sort | mitochondrial inner membrane protein letm1 modulates cristae organization through its letm domain |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7058069/ https://www.ncbi.nlm.nih.gov/pubmed/32139798 http://dx.doi.org/10.1038/s42003-020-0832-5 |
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