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  3. Molecular model of the mitochondrial genome segregation machinery in Trypanosoma brucei
 

Molecular model of the mitochondrial genome segregation machinery in Trypanosoma brucei

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BORIS DOI
10.7892/boris.111274
Date of Publication
January 12, 2018
Publication Type
Article
Division/Institute

Departement für Chemi...

Institut für Zellbiol...

Institut für Anatomie...

Author
Hoffmann, Anneliese
Institut für Zellbiologie (IZB)
Käser, Sandro
Departement für Chemie und Biochemie (DCB)
Jakob, Martin
Institut für Zellbiologie (IZB)
Amodeo, Simonaorcid-logo
Institut für Zellbiologie (IZB)
Peitsch, Camille Françoise
Institut für Anatomie
Týč, Jiří
Vaughan, Sue
Zuber, Benoîtorcid-logo
Institut für Anatomie
Schneider, André
Departement für Chemie und Biochemie (DCB)
Ochsenreiter, Torsten
Institut für Zellbiologie (IZB)
Subject(s)

600 - Technology::610...

500 - Science::570 - ...

500 - Science::540 - ...

Series
Proceedings of the National Academy of Sciences of the United States of America - PNAS
ISSN or ISBN (if monograph)
0027-8424
Publisher
National Academy of Sciences NAS
Language
English
Publisher DOI
10.1073/pnas.1716582115
PubMed ID
29434039
Description
In almost all eukaryotes mitochondria maintain their own genome. Despite the discovery more than 50 years ago still very little is known about how the genome is properly segregated during cell division. The protozoan parasite Trypanosoma brucei contains a single mitochondrion with a singular genome the kinetoplast DNA (kDNA). Electron microscopy studies revealed the tripartite attachment complex (TAC) to physically connect the kDNA to the basal body of the flagellum and to ensure proper segregation of the mitochondrial genome via the basal bodies movement, during cell cycle. Using super-resolution microscopy we precisely localize each of the currently known unique TAC components. We demonstrate that the TAC is assembled in a hierarchical order from the base of the flagellum towards the mitochondrial genome and that the assembly is not dependent on the kDNA itself. Based on biochemical analysis the TAC consists of several non-overlapping subcomplexes suggesting an overall size of the TAC exceeding 2.8 mDa. We furthermore demonstrate that the TAC has an impact on mitochondrial organelle positioning however is not required for proper organelle biogenesis or segregation.
Handle
https://boris-portal.unibe.ch/handle/20.500.12422/158367
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File(s)
FileFile TypeFormatSizeLicensePublisher/Copright statementContent
Hoffmann-et-al.pdftextAdobe PDF1.32 MBpublishedOpen
20180216_MedienmitteilungUniBE_Mitochondrien.pdftextAdobe PDF87.76 KBhttps://www.ub.unibe.ch/services/open_science/boris_publications/index_eng.html#collapse_pane631832supplementalOpen
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