Search Results (154)

Quiescence is a reversible, non-proliferative cellular state that enables survival under nutrient limitation while preserving the capacity to resume growth. Rather than representing a passive default, quiescence is an actively regulated program conserved from unicellular eukaryotes to metazoans. This review focuses on the nuclear mechanisms underlying quiescence entry, maintenance, and exit, with primary emphasis on mechanistic insights from yeast models while highlighting conserved principles in multicellular systems. Across species, quiescence is characterized by global transcriptional repression, chromatin compaction, and the extensive reorganization of nuclear architecture, coordinated by nutrient-sensing pathways centered on TOR/mTOR signaling. We discuss how transcriptional reprogramming is achieved through redistribution of RNA polymerases, dynamic transcription factor activities, and large-scale remodeling of histone modifications, alongside repressive chromatin formation. In parallel, post-transcriptional mechanisms—including intron retention, alternative polyadenylation, and accumulation of non-coding RNAs—fine-tune gene expression while limiting biosynthetic output. We further examine how changes in nuclear organization, such as nucleolar condensation, condensin-mediated chromosome rearrangements, and telomere hyperclusters, support long-term viability and genome stability. Collectively, this review highlights nuclear dynamics as an integrative regulatory layer that links metabolic state to cellular identity, adaptability, and long-term survival, with broad implications for development, stem cell function, and disease. Full article

The literature on the toxicity of silver metal has increased in recent years. However, these studies differ in terms of silver forms, test organisms and exposure times. This makes it difficult to compare results and hinders the development of reliable guidelines on silver toxicity. This study presents a systematic meta-analysis to clarify the comparative toxicity of AgNO₃ and AgNPs on a wide range of biodiversity species, including prokaryotes, unicellular eukaryotes, invertebrates, fish, and terrestrial organisms. We screened 1117 studies published between 1945 and 2024, systematically applied the screening criteria and analyzed 28 data sets from 11 studies that met the eligibility and data quality criteria. The findings demonstrate that AgNO₃ exhibits higher toxicity than AgNPs in most cases, and this effect is particularly pronounced in various organisms. Furthermore, exposure duration is found to be a critical determinant, creating significant differences in both short-term (from 3 h) and long-term (96 h and above) exposures. This study demonstrates that silver toxicity is dependent on forms of silver, and shaped by exposure dose, time-dependent and organism types. A key point in this study is that the evidence base covers the years representing the broadest temporal scope among comparable studies. The results provide a quantitative synthesis of the existing literature, allowing for the identification of generalizable trends regarding the ecotoxicological effects of silver and shed light on the environmental risk assessment processes of silver forms. Full article

TPPP (tubulin polymerization promoting protein)-like proteins are found throughout the living world. The individual members of this protein family are distinguished according to how many times and how completely their characteristic structural element, the p25alpha domain, is found in them. Phylogenomic occurrences of the members of the family differ from each other. Animals, fungi, algae, and various groups of unicellular organisms have their characteristic proteins. The two phylogenomic multi-supergroups, Opimoda+ and Diphoda+, show very different patterns in the occurrence of TPPP types. By using BLAST search in protein and nucleotide databases, we found that the previously known phylogenomic distribution is not strictly true, e.g., fungal type TPPPs are not only found in fungi. We primarily analyzed the Opisthokonta clade but also examined broader relationships. It was confirmed that the occurrence of TPPPs/genes is linked to the presence of the eukaryotic flagellum. A TPPP that contains the entire p25alpha domain twice and occurs only in Opisthokonta was identified. We also identified a TPPP in choanoflagellates and in the uncertainly classified Opisthokonta Tunicaraptor unikontis, which was previously known only in the Diphoda+ clade. On the other hand, we found an Opisthokonta (Opimoda+)-specific TPPP in a Heterolobosea (Diphoda+). Based on these results, we need to rethink the evolutionary history of TPPPs. Full article

Resolving the eukaryotic tree of life (eToL) remains a fundamental challenge in biology. Much of eukaryotic phylogenetic diversity is occupied by unicellular microbial eukaryotes (i.e., protists). Among these, the phylogenetic positions of a significant number of lineages remain unresolved due to limited data and ambiguous traits. To address this issue, we introduce the term “PUPAs” (protists with uncertain phylogenetic affiliations) to collectively describe these lineages, instead of using vague or inconsistent labels, such as incertae sedis or orphan taxa. Historically, protists were classified based solely on morphological features, and many with divergent cell structures were left unplaced in the eToL. With the advent of sequence-based approaches, the phylogenetic affiliations of some PUPAs have been clarified using molecular markers, such as small subunit ribosomal DNA. The combination of technological progress and continuous efforts to cultivate diverse protists, including PUPAs and novel protists, now enables phylogenetic analyses based on hundreds of proteins, providing their concrete placements in the eToL. For example, these advances have led to the discovery of new deep-branching lineages (e.g., Hemimastigophora), the resolution of relationships among major groups (e.g., Microheliella, which linked Cryptista and Archaeplastida), and insights into evolutionary innovations within specific clades (e.g., Glissandra). In this review, we summarize current consensus in eukaryotic phylogeny and highlight recent findings on PUPAs whose phylogenetic affiliations have been clarified. We also discuss a few lineages for which the phylogenetic homes remain unsettled, the evolutionary implications of these discoveries, and the remaining challenges in resolving the complete eToL. Full article

This study was conducted in Armenia and included 32 pregnant women with TV infection and 30 healthy controls. The vaginal virome includes viruses that infect human cells and unicellular eukaryotes such as Trichomonas vaginalis (TV). Among these are Trichomonas vaginalis viruses (TVVs), double-stranded RNA viruses from the Totiviridae family, and giant DNA viruses that replicate in protozoa. This study investigated the presence of TVVs and giant protozoan viruses in pregnant women with trichomoniasis in Armenia and explored their potential associations with adverse pregnancy outcomes. Vaginal and urethral samples were collected from 32 pregnant women with confirmed TV infection and 30 healthy pregnant controls. TVVs and giant viruses (Marseilleviridae, Mimiviridae, Phycodnaviridae) were detected using qRT-PCR. Viral RNA and DNA were extracted from clinical samples and TV cultures, followed by quantification and gene expression analysis. Selected TVVs were visualized via scanning electron microscopy. All TV-positive women carried at least one TVV strain, with 94% harboring multiple TVV types and TVV4 being the most common. TV infection was significantly associated with preterm birth and premature rupture of membranes (PPROM). Giant viruses were identified in all TV-positive cases but in only 40% of controls. Marseilleviridae gene expression was observed in TV cultures, suggesting possible interactions. These findings highlight a potential role for protozoan viruses in reproductive complications and warrant further investigation. Full article

Dunaliella salina, a unicellular and eukaryotic alga, has been found to be one of the most salt-tolerant eukaryotes with a wide range of practical applications. To elucidate the underlying molecular mechanisms of D. salina in response to salinity stress, we performed transcriptome sequencing on samples under different stress conditions. A total of 82,333 unigenes were generated, 4720, 1111 and 2611 differentially expressed genes (DEGs) were identified under high salt stress, oxidative stress and hypertonic stress, respectively. Our analysis revealed that D. salina responds to salinity stress through a complex network of molecular mechanisms. Under high salt stress, starch degradation is regulated by AMY (α-amylase) and PYG (glycogen phosphorylase) with alternative expression patterns. This process is hypothesized to be initially constrained by low ATP levels due to impaired photosynthesis. The clustering analysis of DEGs indicated that starch and sucrose metabolism, as well as glycerol metabolism, are specifically reprogrammed under high salt stress. Glycerol metabolism, particularly involving GPDHs, plays a crucial role in maintaining osmotic balance under salinity stress. Key glycerol metabolism genes were up-regulated under salinity conditions, indicating the importance of this pathway in osmotic regulation. The G3P shuttle, involving mitochondrial GPDHs (c25199_g1 and c23777_g1), contributes to redox imbalance management under high salt, oxidative and hypertonic stresses. Notably, c23777_g1 is involved in the G3P shuttle under high salt, oxidative and hypertonic stresses, while c25199_g1 is specifically induced by hypertonic stress. The R2R3-MYB gene (c23845_g1) may respond to different effects of salinity stress by regulating the transcription of ROS-related genes. Our study provides a detailed understanding of the molecular responses of D. salina to salinity stress. We reveal the critical roles of starch and sucrose metabolism, glycerol metabolism and transcription factors in the D. salina adaptation to salinity. Full article

Photosynthetic eukaryotes have shaped the Earth’s biosphere by producing oxygen and organic compounds using light energy in specialized organelles called plastids. Plastids evolved from free-living cyanobacteria ingested by heterotrophic unicellular eukaryotes. Two such independent engulfment processes, called cyanobacterial endosymbioses, have been reported. The first gave rise to primary plastids and three Archaeplastida lineages: glaucophytes, red algae, and green algae with land plants, whereas the second resulted in chromatophores in the rhizarian amoeba Paulinella. Importantly, Archaeplastidans donated their plastids to many protist groups, further spreading photosynthesis across the tree of life. To reveal complex plastid evolution, we performed comprehensive phylogenetic and molecular clock analyses using new fossil calibrations and the largest number yet of plastid-encoded proteins from 108 taxa, representing diverse photosynthetic organisms. Our results indicate that primary plastids evolved prior to 2.1–1.8 Ga, i.e., before glaucophytes diverged from other Archaeplastidans, and Paulinella chromatophores were likely before 292–266 Ma. Red and green algae were engulfed by cryptophyte and chlorarachniophyte ancestors between 1.7–1.4 Ga and 1.1–1.0 Ga, respectively; the former subsequently triggered plastid transfers to other eukaryotes. We also examined the impact of molecular clocks and calibration sets on age estimates, showing that clocks are the main source of variation. Full article

Microalgae are microscopic unicellular organisms that inhabit marine, freshwater, and moist terrestrial ecosystems. The vast number and diversity of microalgal species provide a significant reservoir of biologically active compounds, highly promising for biomedical applications. Diatoms are unicellular eukaryotic algae belonging to the class Bacillariophyceae. They possess intricately structured silica-based cell walls, which contain long-chain polyamines that play important roles in the formation of silica. Long-chain polyamines are uncommon polyamines found only in organisms that produce biosilica. Diatomite, which is a marine sediment of the remains of the silica skeleton of diatoms, could be an abundant source of biogenic silica that can easily be converted to silica particles. This concise review focuses on the biofabrication of polyamine-based nanosilica from diatoms and highlights the possibility of utilizing diatom biosilica as a nanocarrier for drug and siRNA delivery, bioimaging, and bone tissue engineering. The challenges that may affect diatom production, including environmental stresses and climate change, are discussed together with the prospect of increasing diatom-based biosilica production with the desired nanostructures via genetic manipulation. Full article

The free-living amoeba Acanthamoeba castellanii is a unicellular eukaryote distributed in a wide range of soil or aquatic environments, either natural or human-made, such as rivers, lakes, drinking water, or swimming pools. Besides its capacity to transport potential pathogens, such as bacteria or viruses, Acanthamoeba spp. can have intrinsic pathogenic properties by causing severe infections at the ocular and cerebral level, named granulomatous amoebic encephalitis and amoebic keratitis, respectively. During its life cycle, A. castellanii alternates between a vegetative and mobile form, named the trophozoite, and a resistant, latent, and non-mobile form, named the cyst. The cyst wall of Acanthamoeba is double-layered, with an inner endocyst and an outer ectocyst, and is mainly composed of cellulose and proteins. The resistance of cysts to many environmental stresses and disinfection treatments has been assigned to the presence of cellulose. The current review aims to present the importance of this glycopolymer in Acanthamoeba cysts and to further report the pathways involved in encystment and excystment. Full article

This study explores the biogeographic processes shaping the distribution of benthic foraminifera along a salinity gradient in the Contaco Estuary, southeastern Pacific, Chile. The primary aim was to evaluate the applicability of key ecological paradigms—Rapoport’s rule, the mid-domain effect, ecotones, and source–sink dynamics—to unicellular eukaryotes in estuarine environments. A 1550 m longitudinal transect, sampled at 50 m intervals, revealed a pronounced salinity-driven pattern in species richness and diversity, with calcareous taxa dominating euhaline zones and agglutinated taxa thriving in brackish and freshwater areas. Source–sink dynamics were not supported, as beta diversity analyses identified turnover as the dominant driver, highlighting species replacement along the salinity gradient. Evidence of a longitudinal Rapoport effect was observed, with broader distribution ranges in low-salinity environments, reflecting adaptations to suboptimal conditions. Contrary to predictions, the mid-domain effect was not supported, as foraminiferal richness showed a monotonic decline. These findings extend macroecological principles to microbial communities, emphasizing deterministic processes in shaping estuarine diversity. This research provides a robust framework for understanding biodiversity patterns in dynamic ecosystems, offering valuable insights for conservation and ecological monitoring. Full article

Lipophagy is a selective degradation of lipid droplets in lysosomes or vacuoles. Apart from its role in generating energy and free fatty acids for membrane repair, growth, and the formation of new membranes, lipophagy emerges as a key player in other cellular processes and disease pathogenesis. While fungal, plant, and algal cells use microlipophagy, the most prominent form of lipophagy in animal cells is macrolipophagy. However, recent studies showed that animal cells can also use microlipophagy to metabolize their lipid droplets. Therefore, to no surprise, microlipophagy is conserved from simple unicellular to the most complex multicellular eukaryotes, and many eukaryotic cells can operate both forms of lipophagy. Macrolipophagy is the most studied and better understood at the molecular level, while our understanding of microlipophagy is very sparse. This review will discuss microlipophagy from the perspective of its conservation in eukaryotes and its importance in diseases. To better appreciate the conserved nature of microlipophagy, different organisms and types of cells in which microlipophagy has been reported are also shown in a tabular form. We also point toward the gaps in our understanding of microlipophagy, including the signaling behind microlipophagy, especially in the cells of complex multicellular organisms. Full article

Diatoms are single-celled photosynthetic eukaryotes responsible for CO₂ fixation and primary production in aquatic ecosystems. The cosmopolitan marine diatom Coscinodiscus granii can form seasonal blooms in coastal areas and interact with various microorganisms, including the parasitic oomycete Lagenisma coscinodisci. This unicellular eukaryote is mainly present in the northern hemisphere as an obligate parasite of the genus Coscinodiscus. Understanding the interplay of abiotic factors such as temperature and biotic factors like parasitism on algal physiology is crucial as it dictates plankton community composition and is especially relevant during environmental changes and warming events. This study investigates the impact of two temperatures, 13 °C and 25 °C, on Coscinodiscus granii under laboratory conditions. A decreased infection rate of the parasite was observed at the elevated temperature. Comparative metabolomic analysis using UHPLC-HRMS revealed that temperature and parasitism significantly affect the algal cell metabolome. Abundances of metabolites related to sulfur metabolism, including cysteinoleic acid and dimethylsulfoniopropionate, as well as molecules linked to fatty acid metabolism, e.g., carnitine, acetylcarnitine, and eicosapentanoic acid, significantly increase in cells grown at a higher temperature, suggesting the enhanced rate of metabolism of host cells as the temperature rises. Our study reveals how temperature-induced metabolic changes can influence host–parasite dynamics in a changing environment. Full article

The human gut is a complex ecosystem that supports billions of living species, including bacteria, viruses, archaea, phages, fungi, and unicellular eukaryotes. Bacteria give genes and enzymes for microbial and host-produced compounds, establishing a symbiotic link between the external environment and the host at both the gut and systemic levels. The gut microbiome, which is primarily made up of commensal bacteria, is critical for maintaining the healthy host’s immune system, aiding digestion, synthesizing essential nutrients, and protecting against pathogenic bacteria, as well as influencing endocrine, neural, humoral, and immunological functions and metabolic pathways. Qualitative, quantitative, and/or topographic shifts can alter the gut microbiome, resulting in dysbiosis and microbial dysfunction, which can contribute to a variety of noncommunicable illnesses, including hypertension, cardiovascular disease, obesity, diabetes, inflammatory bowel disease, cancer, and irritable bowel syndrome. While most evidence to date is observational and does not establish direct causation, ongoing clinical trials and advanced genomic techniques are steadily enhancing our understanding of these intricate interactions. This review will explore key aspects of the relationship between gut microbiota, eubiosis, and dysbiosis in human health and disease, highlighting emerging strategies for microbiome engineering as potential therapeutic approaches for various conditions. Full article

Meta-analysis is a beneficial approach to reevaluating the outcomes of independent previous studies in the same scope. Saccharomyces cerevisiae, or the baker’s yeast, is a commonly used unicellular and eukaryotic model organism. In this study, 12 evolved S. cerevisiae strains that became resistant to diverse stress conditions (boron, caffeine, caloric restriction, cobalt, coniferyl aldehyde, ethanol, iron, nickel, oxidative stress, 2-phenylethanol, and silver stress) by adaptive laboratory evolution were reassessed to reveal the correlated stress/stressor clusters based on their transcriptomic and stress–cross-resistance data. Principal Component Analysis (PCA) with k-means clustering was performed. Five clusters for the transcriptomic data of strains and six clusters for cross-resistance stressors were identified. Through statistical evaluations, critical genes pertinent to each cluster were elucidated. The pathways associated with these genes were investigated using the KEGG database. The findings demonstrated that caffeine and coniferyl aldehyde stressors exhibit clear distinctions from other stressors in terms of both physiological stress-cross-resistance responses and transcriptomic profiles. Pathway analysis showed that ribosome biogenesis was downregulated, and starch and sucrose metabolism was upregulated across all clusters. Gene and pathway analyses have shown that stressors lead to distinct changes in yeast gene expression, and these alterations have been systematically documented for each cluster. Several of the highlighted genes are pivotal for further exploration and could potentially clarify new aspects of stress response mechanisms and multiple stress resistance in yeast. Full article

Microalgae are a substantial group of unicellular prokaryotic and eukaryotic marine organisms. Due to their high protein content of 50–70%, microalgae have the potential to become a sustainable alternative protein source, as well as aiding in the development of bioactive peptide-based nutraceuticals. A series of major steps are involved in the production of peptides from microalgae, which include the disruption of the microalgal cell wall, the hydrolysis of proteins, and the extraction or isolation of peptides derived from hydrolysis. Physical methods of cell wall disruptions are favored due to the ability to obtain high-quality protein fractions for peptide production. Bioactive peptides are protein fragments of two to twenty amino acid residues that have a beneficial impact on the physiological functions or conditions of human health. Strong scientific evidence exists for the in vitro antioxidant, antihypertensive, and anti-atherosclerotic properties of microalgal peptides. This review is aimed at summarizing the methods of producing microalgal peptides, and their role and mechanisms in improving cardiovascular health. The review reveals that the validation of the physiological benefits of the microalgal peptides in relation to cardiovascular disease, using human clinical trials, is required. Full article