- Research article
- Open Access
RNA interference screen reveals a high proportion of mitochondrial proteins essential for correct cell cycle progress in Trypanosoma brucei
© Mbang-Benet et al.; licensee BioMed Central. 2015
- Received: 20 March 2014
- Accepted: 30 March 2015
- Published: 15 April 2015
Trypanosomatid parasites possess a single mitochondrion which is classically involved in the energetic metabolism of the cell, but also, in a much more original way, through its single and complex DNA (termed kinetoplast), in the correct progress of cell division. In order to identify proteins potentially involved in the cell cycle, we performed RNAi knockdowns of 101 genes encoding mitochondrial proteins using procyclic cells of Trypanosoma brucei.
A major cell growth reduction was observed in 10 cases and a moderate reduction in 29 other cases. These data are overall in agreement with those previously obtained by a case-by-case approach performed on chromosome 1 genes, and quantitatively with those obtained by “high-throughput phenotyping using parallel sequencing of RNA interference targets” (RIT-seq). Nevertheless, a detailed analysis revealed many qualitative discrepancies with the RIT-seq-based approach. Moreover, for 37 out of 39 mutants for which a moderate or severe growth defect was observed here, we noted abnormalities in the cell cycle progress, leading to increased proportions of abnormal cell cycle stages, such as cells containing more than 2 kinetoplasts (K) and/or more than 2 nuclei (N), and modified proportions of the normal phenotypes (1N1K, 1N2K and 2N2K).
These data, together with the observation of other abnormal phenotypes, show that all the corresponding mitochondrial proteins are involved, directly or indirectly, in the correct progress or, less likely, in the regulation, of the cell cycle in T. brucei. They also show how post-genomics analyses performed on a case-by-case basis may yield discrepancies with global approaches.
- Trypanosoma brucei
- RNA interference
- Cell cycle
Trypanosomatids are flagellated protozoan parasites that belong to the Order of Kinetoplastida. Three of them are human pathogens: Trypanosoma brucei, responsible for the African human trypanosomiasis also known as sleeping sickness, Trypanosoma cruzi, the agent of Chagas’ disease in Latin America, and Leishmania sp., responsible for leishmaniases in many countries throughout the world. In addition to their importance in public health, the cell and molecular biology of these divergent eukaryotes is of great interest, and their study has revealed many original features. For example, the gene organization as large polycistronic-like clusters reminding that of prokaryotes is unique among Eukaryotes [1,2], and is thought to be related with the near-absence of RNA PolII promoters and transcriptional regulation . The 26 Mb genome of T. brucei contains 9302–11100 predicted genes [4,5]. According to GeneDB , 4539 and 575 CDSs (Coding DNA Sequences) are annotated as encoding ‘hypothetical proteins, conserved’ and ‘hypothetical proteins, unlikely’, respectively. Several large studies using different approaches based on RNA interference (RNAi) have been reported with the aim of (i) giving clues on the function of the different CDSs in this parasite, (ii) finding regulators of the cell cycle progress, (iii) opening new avenues for drug design [7-10]. Two studies are of particular interest for the present study: (i) a case-by-case approach, in which almost all the CDSs of chromosome 1 were individually targeted by RNAi ; and (ii) a global approach with an 11× − coverage RNAi plasmid library  made of randomly sheared genomic DNA and cloned in a vector for the Tet-inducible expression of dsRNA .
Among many singularities, trypanosomatids possess a single mitochondrion containing a complex mitochondrial DNA organized in a dense network and termed kinetoplast. The kinetoplast is an essential organelle, not only because it contains a highly specialized form of mitochondrial DNA but also because its duplication and segregation are tightly associated to correct cell cycle progress, in particular cytokinesis [12-14]. The molecular mechanisms governing this link between cytokinesis and the segregation of the kinetoplast and the basal body of the single flagellum are slowly being elucidated, but much remains to be done [15,16]. The T. brucei mitochondrial proteome has been extensively and rigorously analyzed , which allowed the development of high quality multiparametric analyses in bio-informatics . Our starting hypothesis was that, by inhibiting the expression of mitochondrial proteins, we should be able to identify essential proteins associated with this part of the cell cycle in trypanosomatids, defined from cell cycle-specific phenotypes and/or growth reduction. Here, we propose a methodical analysis of the effects of 101 RNAi knockdowns targeting mitochondrial proteins, with the primary aim of determining their potential involvement into cell growth and cell division.
Characteristics of the mitochondrial CDS cohort
This study reports the results of 101 individual RNAi knockdowns performed in procyclic forms (PCF) of T. brucei and targeting proteins for which the mitochondrial localization was predicted “with high confidence” in a previous study , and for (most of) which the annotation in the T. brucei genome database GeneDB  was “Hypothetical protein, conserved” at the start of the study. At the time of writing, new annotations have been proposed for a number of these CDSs (See Additional file 1). All the targeted proteins belong to the mitochondrial protein inventory ‘MitoCarta’ ). Moreover, all 101 CDSs but two (Tb10.61.1810 and Tb927.7.2990, code name in our study: T217 and T320) were also included in a global approach of “high-throughput phenotyping using parallel sequencing of RNA interference targets” (RIT-seq) developed after the start of our study . Finally, five of the analyzed CDSs were included in a ‘semi-systematic’ RNAi study focused on chromosome 1 of T. brucei but utilizing bloodstream forms (BSF) .
Effect of RNAi knockdowns on cell growth
Summary of the concordance observed in the frequencies of cell growth phenotypes between our study and previous studies
Alsford et al. (2011) [ 8 ]
No growth reduction (N = 68)
Severe growth reduction (N = 3)a
Moderate growth reduction (N = 22)
Normal growth (N = 43)
Growth defect (N = 19)
No growth reduction (N = 19)
Subramaniam et al. (2006) [ 7 ]
Severe growth retardationc (N = 2)
No growth reductiond (N = 1)b
Severe growth reductiond (N = 1)
No growth reductionc (N = 3)
No growth reductiond (N = 3)
We then compared our data with those obtained in PCFs using the global approach of RIT-seq : 70 out of our 99 CDSs included in that study were considered not to be associated with growth defects, while 29/99 lead to a growth reduction. These figures appear to be in the same order of magnitude as ours; but this apparent concordance hides significant differences which appear when comparing the results in details (Additional file 1). Indeed, the RIT-seq study reported a cell growth reduction for 19/62 RNAi knockdowns which we classified as having no effect. Conversely, no effect was noted in the RIT-seq study for 22/29 RNAi knockdowns which we classified as having a moderate effect, and for 3/10 which, in our hands, yielded a severe growth reduction. Therefore, a high degree of discrepancy actually exists between both data sets, concerning 44/99 compared proteins. One possible source of these discrepancies is that our PCFs were cultivated in vitro for a long time whereas in the RIT-seq study, Alsford et al. used induced PCFs directly deriving from BSFs. Discrepancies were significantly lower when we compared our data to those obtained from individual RNAi knockdowns in the literature [9,19-26]. Indeed, this comparison showed a concordance between both datasets in 8/11 cases (see Additional file 1); whereas for three genes (T223/ Tb927.4.1660, mitochondrial carrier protein; T171/ Tb927.1.1160 and T179/ Tb927.1.2990), conflicting results were obtained. As regard Tb927.4.1660, in spite of several attempts, Colasante et al.  could not obtain a viable null mutant by double knock-out, nor could they obtain it using RNAi knockdown, even in non-induced condition. By generating cell mutants in which the inducible expression of a single c-Myc-fused version of the gene was possible, they could evaluate the effect of the knockdown of this gene, and therefore inferred that it was essential for the parasite. By contrast, in our hands, mutant parasites for this gene were readily obtained (T223); and no growth reduction was observed after tetracycline induction, despite the efficient silencing of the gene (see Northern blots in Additional file 2B).
Detailed analysis of the major phenotypes associated to a moderate/severe cell growth defect
Cell cycle phenotypes
The percentage of 1N1K cells was increased in only two mutant cell lines (T275 and T305), and similar to the reference cell line in three mutants (T273, T291, T325), but lowered in the 34 others. In the mutant line T245 (gene annotated as Mitochondrial processing peptidase, beta subunit, putative metallo-peptidase, Clan ME, Family M16 in GeneDB, but actually characterized by Acestor et al. as a component of the respiratome ), the reduction in 1N1K cells was particularly drastic, by a 3.6-fold factor as compared with the reference line (i.e. 19% vs. 68.5% of the cells) (Additional file 1); in this line, we also observed a severe reduction of parasite growth and a large excess of multinucleated cells (37.6% of the cells) and multikinetoplastic cells (22.7%, essentially in multinucleated cells), together with zoids (5.4%) and akinetoplastic cells (4.5%), indicating a complete cytokinesis block in spite of continuing nucleus duplication. 2N1K cells, a rare phenotype in the reference cell line (1.1%), were found in increased proportions in 77% of the RNAi mutants (30/39) (Additional file 1). One of the correlations that might be done is the concomitant increase of zoids (0N1K) and of 2N1K cells that may originate from an abnormal division of normal 2N2K cells. Indeed, in the majority of mutants, the increase of both 0N1K and 2N1K were of the same order of magnitude (see for example T178 and T211). However, in eight cases (T195, T271, T272, T278, T287, T288, T316 and T331), the proportions of 2N1K cells were increased without a corresponding increase in zoids, rather suggesting a kinetoplast replication block.
In 25/39 cell lines, abnormally segregating kinetoplasts (either grossly enlarged or “thread-like”) were seen, most often in proportions varying from 0.6 to 6.5%. Even when they were in higher proportions, they could not be associated to any specific ‘cell cycle pattern’. The T245 mutant, which was described here above with a gross cytokinesis block, exhibited as much as 20.3% and 19.8% of cells with enlarged and abnormally segregating kinetoplasts, respectively. The whole of these results strongly suggest a blockage of kinetoplast segregation. The corresponding predicted protein was annotated as a the beta subunit of the Mitochondrial processing peptidase (putative metallo-peptidase, Clan ME, Family M16) in GeneDB, but actually characterized by Acestor et al. as a component of the respiratome, encoding subunits of the cytochrome bc1 complex . This suggests a largely indirect effect, i.e. that the RNAi target is not actually a direct effector of kinetoplast segregation.
Another interesting phenotype affecting the kinetoplast was that of T195, encoding the bona fide alpha subunit of the Mitochondrial processing peptidase . T195 displayed a relatively ‘common’ disruption of the ‘N/K’ pattern but an exceptionally high (6.5%) proportion of 0 K cells. A closer examination showed that 74% of the cells had a kinetoplast greatly reduced in size. The RNAi of several proteins closely associated with the kDNA has been previously shown to cause kDNA loss [30-35]. Yet, what appears here as a defect of the kinetoplast maintenance is again likely one indirect effect secondary to the mis-processing of one mitochondrial imported protein among many. Such an indirect role may be illustrated by a protein named TbLOK1 for loss of kDNA: the authors found that the disappearance of the kDNA occurred well after cell division ceased, arguing that the requirement of TbLOK1 for kDNA maintenance is indirect .
Cytokinesis was also specifically impaired in two mutant lines (T178 and T310), where long dividing (2N2K) cells were seen still joined at their posterior end in significantly high numbers (Figure 3L); it is noteworthy that, to our knowledge, only one protein, spastin, a microtubule-severing enzyme, has been shown to be functionally involved in this final step of cytokinesis in T. brucei, and specifically in bloodstream forms .
A number of abnormal morphological phenotypes could not be specifically related to the cell cycle (see Additional file 1). One of these was the presence, in five mutant lines, of particularly long cells (Figure 3H-I), sometimes twice as long as the non-induced cells (i.e. ~30 μm; Figure 3K-L), in proportions as high as ~26% in lines T291 and T292, ~20% in two other mutants (T177, T178,) and ~8% in one (T293). In mutant T317, these elongated cells were multinucleated (Figure 3I, T317); but in general these phenotypes could not be correlated with any specific ‘N/K’ phenotype: this suggests that, although a tight association between morphogenesis and the cell cycle in T. brucei is well documented , the proteins knocked down here are not necessarily involved in a particular step of the cell cycle.
Finally, in T221, the high increase of 2N1K and zoids was associated to the presence of numerous fragmented (‘apoptotic-like’) nuclei (defined in ) in 16% of the cells (Figure 3J), as well as a distinctive phenotype consisting in half (44%) of the cells being ‘globular’ with pyknotic nuclei (Additional file 1, Additional file 2A for Northern blot), suggesting a profound disruption of unknown essential functions. The abnormal cell division observed here may then well be an indirect consequence of this more global disorder. Morphologically apoptotic nuclei  were seen at a high frequency in only four other lines (T177, T178, T195, and T265; see Additional file 1) but without the ‘globular’ phenotype. However, flow cytometry analysis of the five corresponding cell lines confirmed apoptosis in only two out of five of these (T177 and T178; see Additional file 4).
Among the 101 mitochondrial protein genes knocked down here by RNAi, 39 could be related to a growth defect of the parasite. This number may seem low, but is in agreement with previous reports [7-9]. Several hypotheses may explain the apparent absence of effect seen in the 62 remaining RNAi knockdowns: (i) there may be a functional complementation by another protein, (ii) they may play a role in another differentiation stage of the parasite, (iii) they may simply be non-essential, at least in the experimental conditions used here.
It came as a surprise to us that almost all 39 proteins for which the expression inhibition yielded a growth reduction appeared to be somehow involved in the cell cycle progress. Clearly, the proportion of such proteins is much higher among mitochondrial proteins (here 37/101, i.e. 37%) than among ‘unsorted’ chromosome 1 proteins (6.6%) . Moreover, there are numerous mitochondrial genes on chromosomes 9–11 of which the knock-down may also induce cell cycle perturbation, but these were not included in this study. However, we believe that a proportion of these proteins is pleiotropic and only indirectly involved in the cell cycle progress: the correct progression of this part of the cell cycle may directly or indirectly depend upon a variety of cell activities, e.g. metabolism, signaling cascades, chaperones, etc. The large variety of morphological changes observed here in the mutants indeed suggests that the disruption of the cell cycle might take place upstream, without the corresponding proteins being directly related to it. Also, although the gene targets were analyzed using Trypanofan, we cannot rule out the possibility that off-target effects occurred, particularly for those genes which can be classified as ‘pleiotropic’.
In total, the ‘semi-systematic’ study presented here opens avenues for the characterization of novel proteins involved in the correct cell cycle progress in T. brucei. Our data also show how post-genomics analyses performed on a case-by-case basis may yield discrepancies with global approaches. Finally, they add to the complexity of the picture of cell biology, particularly the cell cycle, of T. brucei, characterized by a tight interdependency of multiple biological processes.
Procyclic forms of the 29–13 line of T. brucei were grown as described  at 27°C in SDM-79 (PAA) supplemented with 10% fetal calf serum, 7 μg.mL−1 hemin, 30 μg.mL−1 hygromycin and 10 μg.mL−1 geneticin.
Selection of targets for RNAi knockdown experiments
We based our work on the results of a proteomic study , which are available online . Our selection criteria were: high confidence assignment of the protein to the mitochondrion , unknown function at the beginning of the study and sufficient length in order to minimize the risk of off-target effects . Progressing chromosome by chromosome in ascending order, all the genes corresponding to these criteria were systematically targeted, until a total of about 100 genes was attained, giving us sufficient confidence in the proportion of genes associated to a cell cycle phenotype: the genes analyzed were present on chromosome 1 to 8.
RNAi knockdown in T. brucei
To design the primers for the production of RNAi constructs, we used the RNAit–target selection script on the T. brucei functional genomics website (TrypanoFAN) [7,42]. Considering oligonucleotide melting temperature and PCR product size, the program is also intended to prevent cross-talk between related gene products in the design of RNAi experiments . The oligonucleotide primers used are all listed in Additional file 5. The different PCR products were cloned into pGEM-Teasy (Promega®) and then into the RNAi vector p2T7tiB/GFP . Transfection and RNAi induction in procyclic forms were performed as described elsewhere . Briefly, 10 μg of linearized plasmid DNA were transfected into 3×107 T. brucei 29–13 procyclic cells. An exponential transfection protocol was used with 1500 V and 25 μF as parameters with a Bio-Rad® Gene pulser 2 electroporator. Transfectants were grown under selective pressure with 5 μg.mL−1 of phleomycin during 8–15 days prior to induction by addition of 1 μg.mL−1 of tetracyclin. Growth curves were compared between the induced and non-induced cell lines.
Definition of the reference line (T280)
For the study of morphological phenotypes, a reference cell line (T280, p2T7-empty) was used for comparison with the mutant cell lines: T280 was transfected with the same RNAi vector containing no insert and then induced in the same manner as the mutant lines. This induced control was considered as the reference cell line; we believe it makes a better control than the uninduced or the wild-type (29–13) cell line of T. brucei.
Total RNAs were extracted with the RNeasy extraction kit (Qiagen) and denatured in a solution of 2.5× MOPS, 9.25% formaldehyde and 50% deionized formamide. RNAs were then incubated 10 min at 65°C and 10 min on ice, before being separated on an agarose gel (1.4% agarose, 6% formaldehyde and MOPS 1×). RNAs were transferred to a nylon membrane and hybridized with a specific probe labeled by random priming with α32-dCTP.
Protocol and criteria for growth reduction definition
The criteria chosen to assess cell growth dynamics used here were as described previously . Briefly, growth of the induced and uninduced culture was followed for up to 8 days after induction, with cell number determined daily using a Z2 Coulter counter (Beckman Coulter®). The numerical data obtained for growth were analyzed according to the following criteria: a defect was recorded if, during the 4 days following induction, cell number in the induced culture was <75% (mild) or <50% (severe) of the uninduced culture for two consecutive days.
Protocol and criteria for definition of cell cycle defects
At day 5 post-induction, cells were fixed in 4% paraformaldehyde and stained with 4′,6-diamidino2-phenylindole (DAPI), air-dried on microscope immunofluorescence slides, and then analysed on a Zeiss Axioplan 2 microscope with a 100× objective equipped with a Photometrics CoolSNAP charge-coupled device camera (Roper Scientific®) driven by Metamorph Software (Molecular Devices®). The numbers of nuclei (N) and kinetoplasts (K) per cell were then counted in 200 cells, allowing determining the position of these cells in the cell cycle progress. Morphological abnormalities of the nuclei and/or kinetoplasts, as well as of the whole cell, were also recorded. All primary phenotypic data were collected blind. These data were then compared to those obtained for the reference cell line described above (T280), where DAPI analysis indicated ~68% cells with one nucleus (N) and one kinetoplast (K) (1N1K cells), ~20% 1N2K cells, and ~7% 2N2K cells, i.e. 95% normal phenotypes. ‘Abnormal’ phenotypes were rare in the reference line: 2.5% 2N1K, 2% zoids (0N1K), <1% multinucleated cells and none for the rest of them. Phenotypes were considered as abnormal in the mutants when they were increased/reduced by a proportion of ± 2.5 SDs, as compared to the induced control (T280). These limits were defined in order to ensure statistical significance to the differences observed. Therefore, an abnormal phenotype was recorded if the following conditions were met: 1N1K <66.1% or >70.9%; 1N2K <13.4% or >29.4%; 2N2K <4.7% or >10.9%; 2N1K >3.8%; multinucleated cells (>2N) >2%; >2N > 2K >0.6%; >2K, 0K and 0N0K >0; and ‘zoids’ (0N) >3.2%.
To determinate the DNA content, a PI staining method was used. For this purpose, cells were washed with PBS, resuspended in 500 μl of iced 70% ethanol, vortexed 1 min and incubated at 4°C. After centrifugation, cells were resuspended in PBS and 10 mg/ml RNAse, placed 20 min at 37°C, centrifuged, incubated 10 – 30 min on ice with 2.5% PI and immediately analysed with a FACSCalibur flow cytometer (Becton Dickinson, San Jose, CA, USA) with the BD CellQuest™ Pro software.
Exposed PS was detected on the outer membrane of cells using the Annexin-V-FLUOS staining kit (Roche®). Cells were washed in PBS and incubated for 10–15 min at 4°C with the incubation buffer of the kit. Fluorescence was measured using an FACS analysis.
The research presented here does not involve vertebrate (including human subject, human material, human data) or any regulated invertebrate.
We thank Frédéric Bringaud (Université Victor Segalen Bordeaux 2) for generously providing the T. brucei 29–13 cell line and T. brucei expression vectors. We were able to get the RNAi vector thanks to TrypanoFAN, the T. brucei functional genomics website, which is supported by the Wellcome Trust and published in Subramaniam et al.  (director Mark Field). We gratefully acknowledge Vicky Diakou and Julien Cau (RIO Imaging in Montpellier/BioCampus Montpellier) for expert advice and assistance in fluorescence microscopy. DEM was a recipient of a PhD grant from the Fondation Infectiopole Sud (http://www.infectiopolesud.com). This work received specific financial support from the MIE (Emerging Infectious Diseases) program of the CNRS, from the University Montpellier 1 (Bonus Qualité Recherche, 2009) and from the Agence Nationale de la Recherche within the frame of the “Investissements d’avenir” program (ANR-11-LABX-0024-01, “ParaFrap”), the French Ministry of Research and the Centre Hospitalier Universitaire of Montpellier.
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