Basal body structure and cell cycle-dependent biogenesis in Trypanosoma brucei
© Vaughan and Gull. 2016
Received: 22 October 2015
Accepted: 19 January 2016
Published: 8 February 2016
Basal bodies are microtubule-based organelles that assemble cilia and flagella, which are critical for motility and sensory functions in all major eukaryotic lineages. The core structure of the basal body is highly conserved, but there is variability in biogenesis and additional functions that are organism and cell type specific. Work carried out in the protozoan parasite Trypanosoma brucei has arguably produced one of the most detailed dissections of basal body structure and biogenesis within the context of the flagellar pocket and associated organelles. In this review, we provide a detailed overview of the basic basal body structure in T. brucei along with the accessory structures and show how basal body movements during the basal body duplication cycle orchestrate cell and organelle morphogenesis. With this in-depth three-dimensional knowledge, identification of many basal body genes coupled with excellent genetic tools makes it an attractive model organism to study basal body biogenesis and maintenance.
KeywordsBasal body Centriole Flagellum Cilium Flagellar pocket Microtubules Axoneme Trypanosoma brucei
The trypanosomes are a group of protozoa characterised by their possession of a single flagellum and a mass of mitochondrial DNA organised into a kinetoplast, which is connected to the proximal end of the basal bodies [1, 2]. They are members of the Excavata; Phylum Euglenozoa; Class Kinetoplastida; Order Trypansomatida; Family Trypanosomatidae; Genus Trypanosoma. The T. brucei group includes three subspecies: the zoonotic/human parasites T. b. rhodesiense and T. b. gambiense and the animal parasite T. b. brucei. The African trypanosomes are closely related to the South American Trypanosoma cruzi and the global Leishmania parasites . However, Leishmania and T. cruzi produce an amastigote form with a shortened flagellum that appears to have a mainly sensory role. Moreover, this amastigote flagellum bears the same collapsed radial symmetry of the microtubule axoneme (9 + 0, 9v) as the primary cilium of mammalian cells [4, 5].
Basic basal body structure
The transition zone is ~400 nm long and is composed of a doublet arrangement of 9 + 0 microtubules. At the boundary between the triplet 9 + 0 microtubule portion of the basal body and the transition zone, there are a set of transitional fibres, which assemble between the A- and B-tubules of each of the nine doublet microtubules (Fig. 1b4, c; arrow) and these connect with the base of the flagellar pocket membrane . In the lumen of this boundary region, where the transitional fibres are located, there is an acorn structure, which was first described in C. reinhardtii and other flagellated organisms and is a centrin-containing structure [11, 12] (Fig. 1d, e). The rest of the rather long transition zone lumen appears devoid of other organised filamentous structures until the basal plate is reached. Y-linkers project from between the A- and B-tubules of each of the nine doublets throughout the transition zone (Fig. 1b5, 6; arrow) except where the transitional fibres are attached at the very proximal end of the transition zone (Fig. 1b4). Detergent-extracted cytoskeletons allow the visualisation of an additional structure encircling the proximal portion of the transition zone which connects to the Y-linkers (Fig. 1b5; arrow). This cytoskeletal structure is most likely the collarette which is external to the flagellar membrane surrounding the proximal portion of the transition zone . The distal end of the mature basal body is capped by a ~30 nm basal plate; a stack of two rings which contain an outer electron dense ring and an inner electron-lucent lumen. The minus ends of the central pair microtubules are embedded in the distal ring  (Figs. 1b7, 8). The A- and B-tubules of the transition zone extend further and the central pair microtubules extend from the basal plate together forming the 9 + 2 microtubule axoneme (Fig. 1b9). Correlations of protein components of the T. brucei basal body and structures described here are dealt with below. However, it is useful to note that trypanosomes have a full complement of the alpha, beta, gamma and delta tubulin gene family. The trypanosome was also one of the first organisms shown to contain epsilon tubulin and was where the canonical zeta tubulin was identified .
Additional and accessory basal body structures
The trypanosome basal bodies form a master organiser for the surrounding cytoskeleton, membranous structures and organelles (Fig. 2). Hence they have a variety of appendages and accessory structures performing roles in the orchestration of cell architecture in addition to those defining basal body/pro-basal body connections for biogenesis and inheritance. Cellular electron tomography studies have highlighted the three-dimensional organisation of accessory basal body structures located on the 9 + 0 triplet microtubule portion in T. brucei . These consist of a set of striated fibres assembled onto the mature basal body with three striated fibres (SF1, 2, 3) associated with the C-tubule of triplet five and two striated fibres associated with the C-tubule of triplet 6 (SF4, 5) . A subset of these striated fibres connects to four rootlet microtubules (the microtubule quartet (MtQ)) , which originate between the mature basal body and pro-basal body and wrap around the flagellar pocket before inserting into the subpellicular microtubule cytoskeleton (Fig. 2). Electron tomography of cytoskeletal preparations has revealed that there are fine filament connections between the MtQ and the pro-basal body (SV/KG; unpublished).
In trypanosomes, the basal bodies serve another function in ensuring inheritance of the mitochondrial genome. The kinetoplast is physically connected to the proximal end of both the mature basal body and pro-basal body  (Fig. 2) by the tripartite attachment complex (TAC). The TAC represents a set of filaments connecting from the proximal end of each basal body to a specialised area of the outer mitochondrial membrane with a further set of unilateral filaments connecting between the inner mitochondrial membrane and the mitochondrial DNA . This physical connection remains intact throughout cell division and the kinetoplast DNA is replicated in a periodic S phase coincident with basal body duplication [17, 18]. Basal body segregation ensures inheritance of the duplicated mitochondrial DNA to the two daughter cells . There must be extensive re-organisation of the tripartite attachment complex during basal body biogenesis, but how this orchestrated and regulated is not yet clear.
Basal body origins
Trypanosome basal bodies are always associated with a flagellum and their biogenesis, maturation and segregation are linked into the flagellum cycle. There is no encysted or other stage in the life cycle where the basal bodies are reduced to the status of centrioles nor one where the structures are removed entirely as in some amoeba-flagellate organisms such as Physarum or Naegleria [19, 20]. Importantly, one should also note that the basal bodies are never associated with the poles of the spindle or the nuclear envelope. The basal bodies act as master organisers of the cytoplasm, organelle position and cell shape without direct involvement with the nucleus and spindle poles. An intranuclear, fibrous, non-membrane associated, spindle organising centre was identified in a TEM study of mitosis . However, no further ultrastructural or biochemical characterisation has been carried out and it is noteworthy to add that no basal body proteins have been reported to localise to the poles of the mitotic spindle (SV/KG; personal communication).
Basal body life cycle and other functions
Identification of basal body components
Centrioles and basal bodies are structurally highly conserved in the core ninefold symmetrical microtubule and cartwheel structure. However, many differences remain in accessory structures and additional specialised functions in diverse cell types. Bioinformatics analysis of 45 eukaryotic organisms revealed 14 core ancestral centriole proteins and 12 of these (δ−tubulin, centrin 2, WDR16, SAS-4, SAS-6, POC1, CEP164, DIP13, VFL1, CEP76, POC5) are conserved in T. brucei, but no orthologues were identified for CEP135 or Centriolin . CEP135/Bld10 localises to a portion of the cartwheel spokes close to the triplet microtubules in C. reinhardtii and knockdown leads to shortened cartwheel spokes , but it seems unlikely to be part of the spokes themselves, due to the lack of conservation. Both the structure of the cartwheel and function of SAS-6 are conserved in T. brucei and L. major [28, 29]. Proteomic analysis of detergent and salt-extracted flagella preparations of T. brucei, which includes the basal body and pro-basal body, identified 331 proteins of which 208 are trypanosomatid-specific. This proteome identified many putative and confirmed ciliopathy genes in the proteome including 34 genes mapping to 25 loci where ciliary dysfunction has been recorded . Other proteomic analysis of T. brucei flagella has extended this list and validated many of the proteome constituents, including intact isolated flagella with membranes  and enriched flagella membrane fractions, which both contain a small number of basal body proteins .
Notable basal body findings
The trypanosome flagella have proven extraordinarily useful for studies on basal body functions as well as flagella-associated functions. Specific basal body insights have come in the involvement of γ-tubulin in basal body nucleation of the central pair ; the discovery of ζ-tubulin  whose importance is now revealed ; the use of proximal end functions in organelle segregation (mitochondrion/kinetoplast) ; positional information in cell form acquisition, specific inheritance patterns of basal bodies  and the flagellar pocket cytoarchitecture [7, 34, 35].
Strengths and future of basal body research in T. brucei
One of the distinct advantages of working with T. brucei in basal body research is that each basal body and pro-basal body can be unequivocally identified within a cell during cell division and differentiation to distinct cell types. The maintenance of an old flagellum and the formation of a new flagellum alongside in the same cell offer unique opportunities to study assembly and turnover of flagellar components. Cultured T. brucei cells are very easy to grow and quick to generate mutant cell lines. There are very well-developed tools to allow the molecular dissection of basal body functions in T. brucei. These include inducible RNAi, allowing stable cell lines to be generated for lethal genes [36–38] and a genome-wide RNAi study identified lethal and non-lethal genes for the two main life cycle forms and during differentiation . There are also excellent tools for PCR tagging at the endogenous locus by homologous recombination, allowing one to go from PCR amplification to transfection into cells within a day . Indeed, there is a whole-genome tagging project underway, which will undoubtedly identify numerous basal body genes. These unique features, phylogenetic positioning and tools make it an attractive model to study basal body biogenesis.
SV and KG wrote the review and approved the final manuscript. Both authors read and approved the final manuscript.
Work in SV lab is funded by BBSRC, MRC and The Wellcome Trust. This work was supported by the Wellcome Trust [WT066839MA and 104627/Z/14/Z] to KG. We thank the many lab members past and present and specifically Dr. Katie Towers for the summary information in Fig. 1.
The authors declare that they have no competing interests.
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
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