Publication:
Molecular model of the mitochondrial genome segregation machinery in Trypanosoma brucei

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cris.virtualsource.author-orcid94aafd18-8ed9-4bbd-9a9c-5920a2c500f9
cris.virtualsource.author-orcid5c817700-47dc-4939-aa69-7075cb6fa762
datacite.rightsopen.access
dc.contributor.authorHoffmann, Anneliese
dc.contributor.authorKäser, Sandro
dc.contributor.authorJakob, Martin
dc.contributor.authorAmodeo, Simona
dc.contributor.authorPeitsch, Camille Françoise
dc.contributor.authorTýč, Jiří
dc.contributor.authorVaughan, Sue
dc.contributor.authorZuber, Benoît
dc.contributor.authorSchneider, André
dc.contributor.authorOchsenreiter, Torsten
dc.date.accessioned2024-10-25T13:54:17Z
dc.date.available2024-10-25T13:54:17Z
dc.date.issued2018-01-12
dc.description.abstractIn 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.
dc.description.sponsorshipDepartement für Chemie und Biochemie (DCB)
dc.description.sponsorshipInstitut für Zellbiologie (IZB)
dc.description.sponsorshipInstitut für Anatomie
dc.identifier.doi10.7892/boris.111274
dc.identifier.pmid29434039
dc.identifier.publisherDOI10.1073/pnas.1716582115
dc.identifier.urihttps://boris-portal.unibe.ch/handle/20.500.12422/158367
dc.language.isoen
dc.publisherNational Academy of Sciences NAS
dc.relation.ispartofProceedings of the National Academy of Sciences of the United States of America - PNAS
dc.relation.issn0027-8424
dc.relation.organizationDCD5A442BCD7E17DE0405C82790C4DE2
dc.relation.organizationDCD5A442C14DE17DE0405C82790C4DE2
dc.relation.organizationDCD5A442C578E17DE0405C82790C4DE2
dc.relation.organization5EBDFFD4994748B4B44FD17D5E463CFB
dc.relation.schoolDCD5A442C27BE17DE0405C82790C4DE2
dc.subject.ddc600 - Technology::610 - Medicine & health
dc.subject.ddc500 - Science::570 - Life sciences; biology
dc.subject.ddc500 - Science::540 - Chemistry
dc.titleMolecular model of the mitochondrial genome segregation machinery in Trypanosoma brucei
dc.typearticle
dspace.entity.typePublication
dspace.file.typetext
dspace.file.typetext
oaire.citation.endPageE1818
oaire.citation.issue8
oaire.citation.startPageE1809
oaire.citation.volume115
oairecerif.author.affiliationInstitut für Zellbiologie (IZB)
oairecerif.author.affiliationDepartement für Chemie und Biochemie (DCB)
oairecerif.author.affiliationInstitut für Zellbiologie (IZB)
oairecerif.author.affiliationInstitut für Zellbiologie (IZB)
oairecerif.author.affiliationInstitut für Anatomie
oairecerif.author.affiliationInstitut für Anatomie
oairecerif.author.affiliationDepartement für Chemie und Biochemie (DCB)
oairecerif.author.affiliationInstitut für Zellbiologie (IZB)
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unibe.date.licenseChanged2019-10-24 04:49:16
unibe.description.ispublishedpub
unibe.eprints.legacyId111274
unibe.journal.abbrevTitleP NATL ACAD SCI USA
unibe.refereedtrue
unibe.subtype.articlejournal

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