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Pena-Diaz, P.

Publications and source records attributed to Pena-Diaz, P..

4 recordsLinked to original sources

Striated fibre assemblins localise in the feeding groove of the 'typical excavate' Paratrimastix pyriformis

The spatial arrangement of microtubules in the cytoskeleton in the cells of protists has been used for decades for taxonomy and phylogenetic inference at various levels. In contrast, the protein composition of non-microtubular structures is mostly unknown. Exceptions are system I fibers in algae, which are built of striated fiber assemblins (SFAs). Interestingly, SFAs are also components of a range of other, dissimilar structures, playing a role in the cortex of ciliates, cell division in apicomplexans, and adhesion of the parasite Giardia to the intestine. In a broad bioinformatic survey, we show the existence of three ancestral eukaryotic paralogs of SFA, and note that they are present in all "typical excavates": small heterotrophic flagellates bearing a ventral feeding groove. In one representative, Paratrimastix pyriformis, we detected two SFA paralogs using specific antibodies and expansion microscopy. We show that they co-localize selectively with several microtubules and structures attached to the basal body of the posterior flagellum, namely the right microtubular root, B-fiber, C-fiber, and composite fiber. We demonstrate that one of the paralogs self-assembles in vitro into striated filaments which, under negative staining and cryo-electron microscopy, resemble system I fibers as seen in previous studies. Given the facts that all three SFA paralogs appear to be ancestral to most eukaryotic lineages, as is probably the morphology of "typical excavates" with a ventral groove, we speculate that these proteins played roles in the support and development of the feeding apparatus of the last eukaryotic common ancestor. SIGNIFICANCE STATEMENTWe identified three paralogues of intermediate filament-like proteins from the family of striated fiber assemblins in the Last Eukaryotic Common Ancestor (LECA). Using expansion microscopy, we demonstrated that two of these proteins form a complex cytoskeleton that supports the feeding groove of Paratrimastix pyriformis. It is widely accepted that this flagellated protist retains the morphological and feeding characteristics of ancestral eukaryotes. Therefore, our results suggest that the striated fiber assemblin proteins, which form diverse structures in various extant eukaryotes, were initially components of the feeding apparatus in LECA.

microbiology↗

Comprehensive analysis of the microbial consortium in the culture of flagellate Monocercomonoides exilis

Monocercomonoides exilis is the only known amitochondriate eukaryote, making it an excellent model for studying the implications of mitochondrial reduction from a cellular and evolutionary point of view. Although M. exilis is an endobiotic heterotroph, it can grow in vitro, albeit with an uncharacterized and complex prokaryotic community. All attempts to grow M. exilis axenically have been unsuccessful. Here, we use metagenomic sequencing at different time points during culture growth to describe the composition and dynamics of this community. We assembled genomes of 24 from at least the 30 different bacterial species within. Based on DNA read abundances, M. exilis represents less than 1.5%, and the representation of dominant bacterial members changes over time. Genome-scale metabolic reconstruction, differential expression analysis and measurements of metabolites in the media showed that the community depends on organic carbon oxidation, fermentation, and hydrogen production without methanogenesis. This is consistent with the rapid decline of amino acids, nucleotides, glyceraldehyde, lactate, fatty acids, and alcohols in the media. The community depends on recycling the external supply of amino acids since it has a limited capacity to fix nitrogen gas and lacks ammonia oxidizers to close the nitrogen cycle. With the senescence of the culture, we observe changes in the expression of several metabolic pathways in M. exilis, particularly those adapting to starvation. We do not reveal any clear metabolic link to explain the dependence of M. exilis on prokaryotes.

microbiology↗

Characterisation of the SUF FeS cluster machinery in the amitochondriate eukaryote Monocercomonoides exilis

Monocercomonoides exilis is the first eukaryotic organism described as a complete amitochondriate, yet it shares common features with heterotrophic anaerobic/microaerophilic protists, some of which bear divergent mitochondrion-related organelles or MROs. It has been postulated that the retention of these organelles stems from their involvement in the assembly of essential cytosolic and nuclear FeS proteins, whose maturation requires the evolutionarily conserved mitochondrial ISC and cytosolic CIA machineries. The amitochondriate M. exilis lacks genes encoding the ISC machinery yet contains a bacteria-derived SUF system (MeSuf), composed of the cysteine desulphurase SufS fused to SufD and SufU, as well as the FeS scaffolding components MeSufB and MeSufC. Here, we show that expression of the M. exilis SUF genes, either individually or in tandem, can restore the maturation of the FeS protein IscR in the Escherichia coli double mutants of {Delta}sufS {Delta}iscS and {Delta}sufB {Delta}iscUA. In vivo and in vitro studies indicate that purified MeSufB, MeSufC and MeSufDSU proteins interact suggesting that they act as a complex in the protist. MeSufBC can undergo conformational changes in the presence of ATP and assemble FeS clusters under anaerobic conditions in presence and absence of ATP in vitro. Altogether, these results indicate that the dynamically interacting MeSufDSUBC proteins may function as an FeS cluster assembly complex in M. exilis thereby being capable of replacing the organelle-enclosed ISC system of canonical eukaryotes.

biochemistry↗

Reduced mitochondria provide an essential function for the cytosolic methionine cycle

It has been long hypothesised that mitochondrial reduction is intrinsically related to the remodelling of Fe-S clusters assembly. Yet as our knowledge of divergent free-living protists broadens, so does the spectrum of variability within the range of mitochondrial-related organelles (MROs) fundamental functions. We resolved to high precision the MRO proteome of Paratrimastix pyriformis using Localisation of Organelle Proteins by Isotope Tagging (LOPIT) and demonstrate its role in the synthesis of folate derivates bearing one-carbon (1C) units, its link to the glycine cleavage system (GCS) and their only conceivable role as suppliers for the cytosolic methionine cycle, involved in recycling of S-adenosine methionine. This observation provides congruity to the presence of GCS in MROs of free-living anaerobes and its absence in endobionts, which typically lose the methionine cycle and, in the case of oxymonads, also mitochondria.

cell biology↗