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Identification of 30 transition fibre proteins in Trypanosoma brucei reveals a complex and dynamic structure
M. Ahmed, R. Wheeler, J. Týč, S. Shafiq, J. Sunter, S. Vaughan
Jazyk angličtina Země Anglie, Velká Británie
Typ dokumentu časopisecké články
Grantová podpora
Wellcome Trust - United Kingdom
Nigel Groome PhD studentship
211075/Z/18/Z
Wellcome Trust - United Kingdom
Oxford Brookes University
NLK
Free Medical Journals
od 1966 do Před 6 měsíci
Open Access Digital Library
od 1853-01-01
Open Access Digital Library
od 1853-01-01
PubMed
38572631
DOI
10.1242/jcs.261692
Knihovny.cz E-zdroje
- MeSH
- bazální tělíska metabolismus MeSH
- časové faktory MeSH
- cilie genetika metabolismus MeSH
- flagella genetika metabolismus MeSH
- konzervovaná sekvence MeSH
- protozoální proteiny * genetika metabolismus MeSH
- regulace genové exprese MeSH
- transport proteinů MeSH
- Trypanosoma brucei brucei * genetika metabolismus MeSH
- Publikační typ
- časopisecké články MeSH
Transition fibres and distal appendages surround the distal end of mature basal bodies and are essential for ciliogenesis, but only a few of the proteins involved have been identified and functionally characterised. Here, through genome-wide analysis, we have identified 30 transition fibre proteins (TFPs) and mapped their arrangement in the flagellated eukaryote Trypanosoma brucei. We discovered that TFPs are recruited to the mature basal body before and after basal body duplication, with differential expression of five TFPs observed at the assembling new flagellum compared to the existing fixed-length old flagellum. RNAi-mediated depletion of 17 TFPs revealed six TFPs that are necessary for ciliogenesis and a further three TFPs that are necessary for normal flagellum length. We identified nine TFPs that had a detectable orthologue in at least one basal body-forming eukaryotic organism outside of the kinetoplastid parasites. Our work has tripled the number of known transition fibre components, demonstrating that transition fibres are complex and dynamic in their composition throughout the cell cycle, which relates to their essential roles in ciliogenesis and flagellum length regulation.
Department of Biological and Medical Sciences Oxford Brookes University Gipsy Lane Oxford OX3 0BP UK
Peter Medawar Building for Pathogen Research University of Oxford Oxford OX1 3SY UK
Citace poskytuje Crossref.org
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