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A novel component of the mitochondrial genome segregation machinery in trypanosomes

We recently described a new component (TAC102) of the mitochondrial genome segregation machinery (mtGSM) in the protozoan parasite Trypanosoma brucei. T. brucei belongs to a group of organisms that contain a single mitochondrial organelle with a single mitochondrial genome (mt-genome) per cell. The...

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Detalles Bibliográficos
Autores principales: Hoffmann, Anneliese, Jakob, Martin, Ochsenreiter, Torsten
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Shared Science Publishers OG 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5349014/
https://www.ncbi.nlm.nih.gov/pubmed/28357371
http://dx.doi.org/10.15698/mic2016.08.519
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author Hoffmann, Anneliese
Jakob, Martin
Ochsenreiter, Torsten
author_facet Hoffmann, Anneliese
Jakob, Martin
Ochsenreiter, Torsten
author_sort Hoffmann, Anneliese
collection PubMed
description We recently described a new component (TAC102) of the mitochondrial genome segregation machinery (mtGSM) in the protozoan parasite Trypanosoma brucei. T. brucei belongs to a group of organisms that contain a single mitochondrial organelle with a single mitochondrial genome (mt-genome) per cell. The mt-genome consists of 5000 minicircles (1 kb) and 25 maxicircles (23 kb) that are catenated into a large network. After replication of the network its segregation is driven by the separating basal bodies, which are homologous structures to the centrioles organizing the spindle apparatus in many eukaryotes. The structure connecting the basal body to the mt-genome was named the Tripartite Attachment Complex (TAC) owing its name to the distribution across three areas in the cell including the two mitochondrial membranes.
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spelling pubmed-53490142017-03-29 A novel component of the mitochondrial genome segregation machinery in trypanosomes Hoffmann, Anneliese Jakob, Martin Ochsenreiter, Torsten Microb Cell Microbiology We recently described a new component (TAC102) of the mitochondrial genome segregation machinery (mtGSM) in the protozoan parasite Trypanosoma brucei. T. brucei belongs to a group of organisms that contain a single mitochondrial organelle with a single mitochondrial genome (mt-genome) per cell. The mt-genome consists of 5000 minicircles (1 kb) and 25 maxicircles (23 kb) that are catenated into a large network. After replication of the network its segregation is driven by the separating basal bodies, which are homologous structures to the centrioles organizing the spindle apparatus in many eukaryotes. The structure connecting the basal body to the mt-genome was named the Tripartite Attachment Complex (TAC) owing its name to the distribution across three areas in the cell including the two mitochondrial membranes. Shared Science Publishers OG 2016-07-28 /pmc/articles/PMC5349014/ /pubmed/28357371 http://dx.doi.org/10.15698/mic2016.08.519 Text en https://creativecommons.org/licenses/by/4.0/ This is an open-access article released under the terms of the Creative Commons Attribution (CC BY) license, which allows the unrestricted use, distribution, and reproduction in any medium, provided the original author and source are acknowledged.
spellingShingle Microbiology
Hoffmann, Anneliese
Jakob, Martin
Ochsenreiter, Torsten
A novel component of the mitochondrial genome segregation machinery in trypanosomes
title A novel component of the mitochondrial genome segregation machinery in trypanosomes
title_full A novel component of the mitochondrial genome segregation machinery in trypanosomes
title_fullStr A novel component of the mitochondrial genome segregation machinery in trypanosomes
title_full_unstemmed A novel component of the mitochondrial genome segregation machinery in trypanosomes
title_short A novel component of the mitochondrial genome segregation machinery in trypanosomes
title_sort novel component of the mitochondrial genome segregation machinery in trypanosomes
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5349014/
https://www.ncbi.nlm.nih.gov/pubmed/28357371
http://dx.doi.org/10.15698/mic2016.08.519
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