Biogenesis of the mitochondrial DNA inheritance machinery in the mitochondrial outer membrane of Trypanosoma brucei

Research output: Contribution to journalJournal articleResearchpeer-review

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Biogenesis of the mitochondrial DNA inheritance machinery in the mitochondrial outer membrane of Trypanosoma brucei. / Käser, Sandro; Willemin, Mathilde; Schnarwiler, Felix; Schimanski, Bernd; Poveda-Huertes, Daniel; Oeljeklaus, Silke; Haenni, Beat; Zuber, Benoît; Warscheid, Bettina; Meisinger, Chris; Schneider, André.

In: PLoS Pathogens, Vol. 13, No. 12, 12.2017, p. e1006808.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Käser, S, Willemin, M, Schnarwiler, F, Schimanski, B, Poveda-Huertes, D, Oeljeklaus, S, Haenni, B, Zuber, B, Warscheid, B, Meisinger, C & Schneider, A 2017, 'Biogenesis of the mitochondrial DNA inheritance machinery in the mitochondrial outer membrane of Trypanosoma brucei', PLoS Pathogens, vol. 13, no. 12, pp. e1006808. https://doi.org/10.1371/journal.ppat.1006808

APA

Käser, S., Willemin, M., Schnarwiler, F., Schimanski, B., Poveda-Huertes, D., Oeljeklaus, S., Haenni, B., Zuber, B., Warscheid, B., Meisinger, C., & Schneider, A. (2017). Biogenesis of the mitochondrial DNA inheritance machinery in the mitochondrial outer membrane of Trypanosoma brucei. PLoS Pathogens, 13(12), e1006808. https://doi.org/10.1371/journal.ppat.1006808

Vancouver

Käser S, Willemin M, Schnarwiler F, Schimanski B, Poveda-Huertes D, Oeljeklaus S et al. Biogenesis of the mitochondrial DNA inheritance machinery in the mitochondrial outer membrane of Trypanosoma brucei. PLoS Pathogens. 2017 Dec;13(12):e1006808. https://doi.org/10.1371/journal.ppat.1006808

Author

Käser, Sandro ; Willemin, Mathilde ; Schnarwiler, Felix ; Schimanski, Bernd ; Poveda-Huertes, Daniel ; Oeljeklaus, Silke ; Haenni, Beat ; Zuber, Benoît ; Warscheid, Bettina ; Meisinger, Chris ; Schneider, André. / Biogenesis of the mitochondrial DNA inheritance machinery in the mitochondrial outer membrane of Trypanosoma brucei. In: PLoS Pathogens. 2017 ; Vol. 13, No. 12. pp. e1006808.

Bibtex

@article{37606bfc794847e99d3d838f9e561e74,
title = "Biogenesis of the mitochondrial DNA inheritance machinery in the mitochondrial outer membrane of Trypanosoma brucei",
abstract = "Mitochondria cannot form de novo but require mechanisms that mediate their inheritance to daughter cells. The parasitic protozoan Trypanosoma brucei has a single mitochondrion with a single-unit genome that is physically connected across the two mitochondrial membranes with the basal body of the flagellum. This connection, termed the tripartite attachment complex (TAC), is essential for the segregation of the replicated mitochondrial genomes prior to cytokinesis. Here we identify a protein complex consisting of three integral mitochondrial outer membrane proteins-TAC60, TAC42 and TAC40-which are essential subunits of the TAC. TAC60 contains separable mitochondrial import and TAC-sorting signals and its biogenesis depends on the main outer membrane protein translocase. TAC40 is a member of the mitochondrial porin family, whereas TAC42 represents a novel class of mitochondrial outer membrane β-barrel proteins. Consequently TAC40 and TAC42 contain C-terminal β-signals. Thus in trypanosomes the highly conserved β-barrel protein assembly machinery plays a major role in the biogenesis of its unique mitochondrial genome segregation system.",
keywords = "Animals, DNA, Kinetoplast/biosynthesis, DNA, Mitochondrial/biosynthesis, Genome, Mitochondrial, Genome, Protozoan, Humans, Mitochondrial Dynamics, Mitochondrial Membranes/metabolism, Multiprotein Complexes/chemistry, Protein Sorting Signals/genetics, Protozoan Proteins/chemistry, Trypanosoma brucei brucei/genetics",
author = "Sandro K{\"a}ser and Mathilde Willemin and Felix Schnarwiler and Bernd Schimanski and Daniel Poveda-Huertes and Silke Oeljeklaus and Beat Haenni and Beno{\^i}t Zuber and Bettina Warscheid and Chris Meisinger and Andr{\'e} Schneider",
year = "2017",
month = dec,
doi = "10.1371/journal.ppat.1006808",
language = "English",
volume = "13",
pages = "e1006808",
journal = "P L o S Pathogens (Online)",
issn = "1553-7374",
publisher = "public library of science",
number = "12",

}

RIS

TY - JOUR

T1 - Biogenesis of the mitochondrial DNA inheritance machinery in the mitochondrial outer membrane of Trypanosoma brucei

AU - Käser, Sandro

AU - Willemin, Mathilde

AU - Schnarwiler, Felix

AU - Schimanski, Bernd

AU - Poveda-Huertes, Daniel

AU - Oeljeklaus, Silke

AU - Haenni, Beat

AU - Zuber, Benoît

AU - Warscheid, Bettina

AU - Meisinger, Chris

AU - Schneider, André

PY - 2017/12

Y1 - 2017/12

N2 - Mitochondria cannot form de novo but require mechanisms that mediate their inheritance to daughter cells. The parasitic protozoan Trypanosoma brucei has a single mitochondrion with a single-unit genome that is physically connected across the two mitochondrial membranes with the basal body of the flagellum. This connection, termed the tripartite attachment complex (TAC), is essential for the segregation of the replicated mitochondrial genomes prior to cytokinesis. Here we identify a protein complex consisting of three integral mitochondrial outer membrane proteins-TAC60, TAC42 and TAC40-which are essential subunits of the TAC. TAC60 contains separable mitochondrial import and TAC-sorting signals and its biogenesis depends on the main outer membrane protein translocase. TAC40 is a member of the mitochondrial porin family, whereas TAC42 represents a novel class of mitochondrial outer membrane β-barrel proteins. Consequently TAC40 and TAC42 contain C-terminal β-signals. Thus in trypanosomes the highly conserved β-barrel protein assembly machinery plays a major role in the biogenesis of its unique mitochondrial genome segregation system.

AB - Mitochondria cannot form de novo but require mechanisms that mediate their inheritance to daughter cells. The parasitic protozoan Trypanosoma brucei has a single mitochondrion with a single-unit genome that is physically connected across the two mitochondrial membranes with the basal body of the flagellum. This connection, termed the tripartite attachment complex (TAC), is essential for the segregation of the replicated mitochondrial genomes prior to cytokinesis. Here we identify a protein complex consisting of three integral mitochondrial outer membrane proteins-TAC60, TAC42 and TAC40-which are essential subunits of the TAC. TAC60 contains separable mitochondrial import and TAC-sorting signals and its biogenesis depends on the main outer membrane protein translocase. TAC40 is a member of the mitochondrial porin family, whereas TAC42 represents a novel class of mitochondrial outer membrane β-barrel proteins. Consequently TAC40 and TAC42 contain C-terminal β-signals. Thus in trypanosomes the highly conserved β-barrel protein assembly machinery plays a major role in the biogenesis of its unique mitochondrial genome segregation system.

KW - Animals

KW - DNA, Kinetoplast/biosynthesis

KW - DNA, Mitochondrial/biosynthesis

KW - Genome, Mitochondrial

KW - Genome, Protozoan

KW - Humans

KW - Mitochondrial Dynamics

KW - Mitochondrial Membranes/metabolism

KW - Multiprotein Complexes/chemistry

KW - Protein Sorting Signals/genetics

KW - Protozoan Proteins/chemistry

KW - Trypanosoma brucei brucei/genetics

U2 - 10.1371/journal.ppat.1006808

DO - 10.1371/journal.ppat.1006808

M3 - Journal article

C2 - 29287109

VL - 13

SP - e1006808

JO - P L o S Pathogens (Online)

JF - P L o S Pathogens (Online)

SN - 1553-7374

IS - 12

ER -

ID: 391635475