TY - JOUR
T1 - The mitochondrial inner membrane protein LETM1 modulates cristae organization through its LETM domain
AU - Nakamura, Seiko
AU - Matsui, Aiko
AU - Akabane, Shiori
AU - Tamura, Yasushi
AU - Hatano, Azumi
AU - Miyano, Yuriko
AU - Omote, Hiroshi
AU - Kajikawa, Mizuho
AU - Maenaka, Katsumi
AU - Moriyama, Yoshinori
AU - Endo, Toshiya
AU - Oka, Toshihiko
N1 - Funding Information:
We greatly appreciate Atsumi Toyota for supporting the initial experiments of this study. We also thank Hiromi Hirose and Tomie Kameyama for excellent technical assistance. This work was supported by grants to T.O. from Grants-in-Aid for Scientific Research (17H03676) from JSPS, the Strategic Research Foundation Grant-aided Project for Private Universities (S1201003) from MEXT, and a JST CREST (Grant Number JPMJCR12M1).
Publisher Copyright:
© 2020, The Author(s).
PY - 2020/12/1
Y1 - 2020/12/1
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85081300673&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85081300673&partnerID=8YFLogxK
U2 - 10.1038/s42003-020-0832-5
DO - 10.1038/s42003-020-0832-5
M3 - Article
C2 - 32139798
AN - SCOPUS:85081300673
SN - 2399-3642
VL - 3
JO - Communications Biology
JF - Communications Biology
IS - 1
M1 - 99
ER -