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Evolution of heterotrophy in chrysophytes as reflected by comparative transcriptomics

https://doi.org/10.1093/femsec/fiy039
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Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/9780470758472.ch1openalex-snapshot
The Basic Principles of Photosynthetic Energy Storage
inferredcites →https://doi.org/10.1007/978-1-4020-4061-0_18openalex-snapshot
Amino Acid Synthesis in Plastids
inferredcites →https://doi.org/10.1007/bf00601942openalex-snapshot
Der B-vitamin-Bedarf der Chrysophyceen ?Ochromonas danica nom. provis.Pringsheim? und ?Ochromonas malhamensisPringsheim?
inferredcites →https://doi.org/10.1007/bf02015056openalex-snapshot
Relationship between phototrophy and phagotrophy in the mixotrophic chrysophytePoterioochromonas malhamensis
inferredcites →https://doi.org/10.1007/bf02804901openalex-snapshot
Harmful algal blooms and eutrophication: Nutrient sources, composition, and consequences
inferredcites →https://doi.org/10.1007/s00239-004-0353-8openalex-snapshot
Phylogeny and Megasystematics of Phagotrophic Heterokonts (Kingdom Chromista)
inferredcites →https://doi.org/10.1007/s002390010210openalex-snapshot
Dinoflagellate Nuclear SSU rRNA Phylogeny Suggests Multiple Plastid Losses and Replacements
inferredcites →https://doi.org/10.1007/s00248-001-1024-6openalex-snapshot
Nutrient Acquisition and Population Growth of a Mixotrophic Alga in Axenic and Bacterized Cultures
inferredcites →https://doi.org/10.1007/s00294-008-0208-8openalex-snapshot
From chloroplasts to “cryptic” plastids: evolution of plastid genomes in parasitic plants
inferredcites →https://doi.org/10.1007/s00294-017-0761-0openalex-snapshot
Reductive evolution of chloroplasts in non-photosynthetic plants, algae and protists
inferredcites →https://doi.org/10.1007/s00709-011-0269-2openalex-snapshot
The evolutionary phylogeny of the oomycete “fungi”
inferredcites →https://doi.org/10.1016/0968-0004(83)90366-3openalex-snapshot
Monogalactosyldiacylglycerol: The most abundant polar lipid in nature
inferredcites →https://doi.org/10.1016/j.cub.2008.05.042openalex-snapshot
Multiple Genes of Apparent Algal Origin Suggest Ciliates May Once Have Been Photosynthetic
inferredcites →https://doi.org/10.1016/j.cub.2008.06.031openalex-snapshot
Plastid Evolution: Remnant Algal Genes in Ciliates
inferredcites →https://doi.org/10.1016/j.mib.2013.07.003openalex-snapshot
The metabolic roles of the endosymbiotic organelles of Toxoplasma and Plasmodium spp.
inferredcites →https://doi.org/10.1016/j.micinf.2009.12.010openalex-snapshot
Apicoplast: keep it or leave it
inferredcites →https://doi.org/10.1016/j.plipres.2014.02.001openalex-snapshot
Evolution of galactoglycerolipid biosynthetic pathways – From cyanobacteria to primary plastids and from primary to secondary plastids
inferredcites →https://doi.org/10.1016/j.protis.2006.09.004openalex-snapshot
Plastid Genes in a Non-Photosynthetic Dinoflagellate
inferredcites →https://doi.org/10.1016/j.protis.2010.10.003openalex-snapshot
Emerging Diversity within Chrysophytes, Choanoflagellates and Bicosoecids Based on Molecular Surveys
inferredcites →https://doi.org/10.1016/j.tplants.2013.10.004openalex-snapshot
Plastids with or without galactoglycerolipids
inferredcites →https://doi.org/10.1016/s0014-5793(96)01404-4openalex-snapshot
Biosynthesis of isoprenoids in higher plant chloroplasts proceeds via a mevalonate‐independent pathway
inferredcites →https://doi.org/10.1016/s0031-9422(00)84362-9openalex-snapshot
The pathway of nitrogen assimilation in plants
inferredcites →https://doi.org/10.1016/s0960-9822(01)00675-3openalex-snapshot
Chloroplast Evolution: Secondary Symbiogenesis and Multiple Losses
inferredcites →https://doi.org/10.1016/s1360-1385(01)02216-6openalex-snapshot
Galactolipids rule in seed plants
inferredcites →https://doi.org/10.1016/s1434-4610(99)70010-6openalex-snapshot
Phylogenetic Analysis of the SSU rRNA from Members of the Chrysophyceae
inferredcites →https://doi.org/10.1023/b:pres.0000017196.95499.11openalex-snapshot
Sulfur Assimilation and the Role of Sulfur in Plant Metabolism: A Survey
inferredcites →https://doi.org/10.1038/174520b0openalex-snapshot
Cobalamin Requirement in Chrysophyceae
inferredcites →https://doi.org/10.1038/nbt.1883openalex-snapshot
Full-length transcriptome assembly from RNA-Seq data without a reference genome
inferredcites →https://doi.org/10.1038/nrmicro.2016.160openalex-snapshot
Probing the evolution, ecology and physiology of marine protists using transcriptomics
inferredcites →https://doi.org/10.1046/j.1365-2427.2000.00672.xopenalex-snapshot
Mixotrophy in planktonic protists: an overview
inferredcites →https://doi.org/10.1046/j.1529-8817.1999.3561430.xopenalex-snapshot
MIXOTROPHY AND NITROGEN UPTAKE BY PFIESTERIA PISCICIDA (DINOPHYCEAE)
inferredcites →https://doi.org/10.1073/pnas.1614842114openalex-snapshot
Major transitions in dinoflagellate evolution unveiled by phylotranscriptomics
inferredcites →https://doi.org/10.1074/jbc.m009452200openalex-snapshot
Apicomplexan Parasites Possess Distinct Nuclear-encoded, but Apicoplast-localized, Plant-type Ferredoxin-NADP+ Reductase and Ferredoxin
inferredcites →https://doi.org/10.1074/jbc.m209388200openalex-snapshot
Ferredoxin-NADP+ Reductase and Ferredoxin of the Protozoan Parasite Toxoplasma gondii Interact Productivelyin Vitro and in Vivo
inferredcites →https://doi.org/10.1080/09670262.2013.833297openalex-snapshot
Mono- and digalactosyldiacylglycerol composition of dinoflagellates. VII. Evidence against galactolipid production and plastid presence in the heterotrophic, basal dinoflagellate, Oxyrrhis marina
inferredcites →https://doi.org/10.1086/303291openalex-snapshot
Tracing the Thread of Plastid Diversity Through the Tapestry of Life
inferredcites →https://doi.org/10.1093/bioinformatics/btr595openalex-snapshot
RAPSearch2: a fast and memory-efficient protein similarity search tool for next-generation sequencing data
inferredcites →https://doi.org/10.1093/femsec/fiv137openalex-snapshot
Temporal dynamics of the metabolically active rumen bacteria colonizing fresh perennial ryegrass
inferredcites →https://doi.org/10.1093/femsec/fiw106openalex-snapshot
Gene expression characterizes different nutritional strategies among three mixotrophic protists
inferredcites →https://doi.org/10.1093/jexbot/53.370.979openalex-snapshot
The role of glutamine synthetase and glutamate dehydrogenase in nitrogen assimilation and possibilities for improvement in the nitrogen utilization of crops
inferredcites →https://doi.org/10.1093/molbev/msn075openalex-snapshot
Plastid-Derived Genes in the Nonphotosynthetic Alveolate Oxyrrhis marina
inferredcites →https://doi.org/10.1093/molbev/msv134openalex-snapshot
Proposal of a Twin Aarginine Translocator System-Mediated Constraint against Loss of ATP Synthase Genes from Nonphotosynthetic Plastid Genomes
inferredcites →https://doi.org/10.1093/molbev/msv247openalex-snapshot
Proposal of a Twin Aarginine Translocator System-Mediated Constraint against Loss of ATP Synthase Genes from Nonphotosynthetic Plastid Genomes
inferredcites →https://doi.org/10.1093/molbev/msx172openalex-snapshot
A Non-photosynthetic Diatom Reveals Early Steps of Reductive Evolution in Plastids
inferredcites →https://doi.org/10.1093/nar/27.1.29openalex-snapshot
KEGG: Kyoto Encyclopedia of Genes and Genomes
inferredcites →https://doi.org/10.1093/nar/28.1.27openalex-snapshot
KEGG: Kyoto Encyclopedia of Genes and Genomes
inferredcites →https://doi.org/10.1093/nar/gkw1092openalex-snapshot
KEGG: new perspectives on genomes, pathways, diseases and drugs
inferredcites →https://doi.org/10.1098/rstb.2009.0103openalex-snapshot
The endosymbiotic origin, diversification and fate of plastids
inferredcites →https://doi.org/10.1098/rstb.2009.0273openalex-snapshot
The evolution, metabolism and functions of the apicoplast
inferredcites →https://doi.org/10.1104/pp.109.139758openalex-snapshot
The Role of Diglycosyl Lipids in Photosynthesis and Membrane Lipid Homeostasis in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1399-3054.1987.tb09240.xopenalex-snapshot
The light‐harvesting and protective functions of carotenoids in photosynthetic membranes
inferredcites →https://doi.org/10.1111/j.1462-2920.2005.00743.xopenalex-snapshot
High diversity of the ‘ Spumella ‐like’ flagellates: an investigation based on the SSU rRNA gene sequences of isolates from habitats located in six different geographic regions
inferredcites →https://doi.org/10.1111/j.1550-7408.1991.tb04805.xopenalex-snapshot
Mixotrophic Protists In Marine and Freshwater Ecosystems
inferredcites →https://doi.org/10.1111/j.1742-4658.2006.05475.xopenalex-snapshot
Quantitative analysis of the experimental O–J–I–P chlorophyll fluorescence induction kinetics
inferredcites →https://doi.org/10.1111/jeu.12287openalex-snapshot
Small but Manifold – Hidden Diversity in “ Spumella ‐like Flagellates”
inferredcites →https://doi.org/10.1111/jpy.12292openalex-snapshot
Diversity of nitrogen assimilation pathways among microbial photosynthetic eukaryotes
inferredcites →https://doi.org/10.1111/pre.12072openalex-snapshot
Multiple losses of photosynthesis in N itzschia ( B acillariophyceae)
inferredcites →https://doi.org/10.1128/aem.69.3.1442-1451.2003openalex-snapshot
Isolation of Novel Ultramicrobacteria Classified as Actinobacteria from Five Freshwater Habitats in Europe and Asia
inferredcites →https://doi.org/10.1128/ec.00097-06openalex-snapshot
Algae Need Their Vitamins
inferredcites →https://doi.org/10.1146/annurev-arplant-050312-120144openalex-snapshot
The Number, Speed, and Impact of Plastid Endosymbioses in Eukaryotic Evolution
inferredcites →https://doi.org/10.1146/annurev-micro-092412-155741openalex-snapshot
The Algal Past and Parasite Present of the Apicoplast
inferredcites →https://doi.org/10.1146/annurev.arplant.50.1.473openalex-snapshot
THE SHIKIMATE PATHWAY
inferredcites →https://doi.org/10.1146/annurev.arplant.59.032607.092915openalex-snapshot
Plastid Evolution
inferredcites →https://doi.org/10.1186/1471-2105-12-35openalex-snapshot
VennDiagram: a package for the generation of highly-customizable Venn and Euler diagrams in R
inferredcites →https://doi.org/10.1186/1471-2148-5-56openalex-snapshot
Lineage-specific variations of congruent evolution among DNA sequences from three genomes, and relaxed selective constraints on rbcL in Cryptomonas (Cryptophyceae)
inferredcites →https://doi.org/10.1186/1741-7007-4-12openalex-snapshot
The complete plastid genome sequence of the parasitic green alga Helicosporidium sp. is highly reduced and structured
inferredcites →https://doi.org/10.1201/9780849379901.ch15openalex-snapshot
Molecular systematics of the Chrysophyceae and Synurophyceae
inferredcites →https://doi.org/10.1371/journal.pone.0008465openalex-snapshot
Reverse Evolution: Driving Forces Behind the Loss of Acquired Photosynthetic Traits
inferredcites →https://doi.org/10.1371/journal.pone.0096258openalex-snapshot
Transcriptomic Analysis Reveals Evidence for a Cryptic Plastid in the Colpodellid Voromonas pontica, a Close Relative of Chromerids and Apicomplexan Parasites
inferredcites →https://doi.org/10.1371/journal.pone.0168183openalex-snapshot
Quantitative Proteomics Reveals Ecophysiological Effects of Light and Silver Stress on the Mixotrophic Protist Poterioochromonas malhamensis
inferredcites →https://doi.org/10.14806/ej.17.1.200openalex-snapshot
Cutadapt removes adapter sequences from high-throughput sequencing reads
inferredcites →https://doi.org/10.3354/ame01662openalex-snapshot
Influence of nutrients and light on autotrophic, mixotrophic and heterotrophic freshwater chrysophytes
inferredcites →https://doi.org/10.3389/fmicb.2015.00319openalex-snapshot
Gene expression in the mixotrophic prymnesiophyte, Prymnesium parvum, responds to prey availability
inferredcites →https://doi.org/10.4319/lo.1990.35.2.0433openalex-snapshot
Carbon, nitrogen, and phosphorus budgets for the mixotrophic phytoflagellate Poterioochromonas malhamensis (Chrysophyceae) during bacterial ingestion
inferredcites →https://doi.org/10.7717/peerj.2832openalex-snapshot
Comprehensive transcriptome analysis provides new insights into nutritional strategies and phylogenetic relationships of chrysophytes

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.1007/s13127-018-0365-7zenodo-depositor-declared
Genome size of chrysophytes varies with cell size and nutritional mode
inferred← citeshttps://doi.org/10.5281/zenodo.13321623zenodo-depositor-declared
inferred← citeshttps://doi.org/10.1002/bies.202100258openalex-snapshot
Eukaryotic cellular intricacies shape mitochondrial proteomic complexity
inferred← citeshttps://doi.org/10.1007/978-3-030-92499-7_6openalex-snapshot
Reconstructing Dynamic Evolutionary Events in Diatom Nuclear and Organelle Genomes
inferred← citeshttps://doi.org/10.1007/978-3-031-57446-7_5openalex-snapshot
Easier Lost than Found? What We Know about Plastid Genome Reduction
inferred← citeshttps://doi.org/10.1007/s00300-021-02850-3openalex-snapshot
Phylogenetic diversity and dominant ecological traits of freshwater Antarctic Chrysophyceae
inferred← citeshttps://doi.org/10.1007/s10750-022-05075-5openalex-snapshot
Contribution of silica-scaled chrysophytes to ecosystems services: a review
inferred← citeshttps://doi.org/10.1016/b978-0-12-822861-6.00022-4openalex-snapshot
Transcriptomic and metatranscriptomic approaches in phytoplankton: insights and advances
inferred← citeshttps://doi.org/10.1016/b978-0-443-15738-7.00006-4openalex-snapshot
Algae Types and Characteristics
inferred← citeshttps://doi.org/10.1016/j.ejop.2021.125807openalex-snapshot
Winogradsky columns as a strategy to study typically rare microbial eukaryotes
inferred← citeshttps://doi.org/10.1016/j.ejop.2022.125915openalex-snapshot
High molecular diversity in the functional group of small bacterivorous non-scaled chrysomonad flagellates
inferred← citeshttps://doi.org/10.1016/j.ejop.2024.126109openalex-snapshot
Comparison of mixotrophic and heterotrophic chrysomonads of similar size regarding bacterivory and growth rate
inferred← citeshttps://doi.org/10.1016/j.protis.2026.126175openalex-snapshot
Poteriospumella species in Vietnam with remarks on distribution and diversity of the genus
inferred← citeshttps://doi.org/10.1016/j.watres.2022.119299openalex-snapshot
Suppressing cyanobacterial dominance by UV-LED TiO2-photocatalysis in a drinking water reservoir: A mesocosm study
inferred← citeshttps://doi.org/10.1038/s42003-021-01781-3openalex-snapshot
Nutrient-driven genome evolution revealed by comparative genomics of chrysomonad flagellates
inferred← citeshttps://doi.org/10.1073/pnas.1819976116openalex-snapshot
Principles of plastid reductive evolution illuminated by nonphotosynthetic chrysophytes
inferred← citeshttps://doi.org/10.1080/23802359.2021.1923416openalex-snapshot
Complete chloroplast genome of the mixotrophic chrysophyte Poterioochromonas malhamensis (Ochromonadales, Synurophyceae) from Van Lake in Eastern Anatolia
inferred← citeshttps://doi.org/10.1093/gbe/evaa096openalex-snapshot
Genomic Insights into Plastid Evolution
inferred← citeshttps://doi.org/10.1093/gbe/evz155openalex-snapshot
Nephromyces represents a diverse and novel lineage of the Apicomplexa that has retained apicoplasts
inferred← citeshttps://doi.org/10.1093/gbe/evz171openalex-snapshot
Intraspecific Variation in Protists: Clues for Microevolution from Poteriospumella lacustris (Chrysophyceae)
inferred← citeshttps://doi.org/10.1093/ismejo/wrae150openalex-snapshot
Integrated overview of stramenopile ecology, taxonomy, and heterotrophic origin
inferred← citeshttps://doi.org/10.1101/765255openalex-snapshot
The cryptic plastid of Euglena longa defines a new type of non-photosynthetic plastid organelles
inferred← citeshttps://doi.org/10.1111/1365-2745.13732openalex-snapshot
Contribution of microbial photosynthesis to peatland carbon uptake along a latitudinal gradient
inferred← citeshttps://doi.org/10.1128/msphere.00675-20openalex-snapshot
The Cryptic Plastid of Euglena longa Defines a New Type of Nonphotosynthetic Plastid Organelle
inferred← citeshttps://doi.org/10.12688/f1000research.16734.1openalex-snapshot
Draft genome assembly and transcriptome sequencing of the golden algae Hydrurus foetidus (Chrysophyceae)
inferred← citeshttps://doi.org/10.12688/f1000research.16734.2openalex-snapshot
Draft genome assembly and transcriptome sequencing of the golden algae Hydrurus foetidus (Chrysophyceae)
inferred← citeshttps://doi.org/10.12688/f1000research.16734.3openalex-snapshot
Draft genome assembly and transcriptome sequencing of the golden algae Hydrurus foetidus (Chrysophyceae)
inferred← citeshttps://doi.org/10.2139/ssrn.6239041openalex-snapshot
Changes in the protist networks in a Mediterranean coastal lagoon strongly impacted by eutrophication
inferred← citeshttps://doi.org/10.3389/fmars.2021.666160openalex-snapshot
Eco-Evolutionary Perspectives on Mixoplankton
inferred← citeshttps://doi.org/10.3389/fmicb.2019.01498openalex-snapshot
Interaction-Specific Changes in the Transcriptome of Polynucleobacter asymbioticus Caused by Varying Protistan Communities
inferred← citeshttps://doi.org/10.3389/fpls.2020.572703openalex-snapshot
Comparative Plastid Genomics of Non-Photosynthetic Chrysophytes: Genome Reduction and Compaction
inferred← citeshttps://doi.org/10.3389/fpls.2021.758067openalex-snapshot
Molecular Phylogeny and Taxonomy of the Genus Spumella (Chrysophyceae) Based on Morphological and Molecular Evidence
inferred← citeshttps://doi.org/10.5281/zenodo.13321622openalex-snapshot
Trophic guild data for microbial eukaryotes
inferred← citeshttps://doi.org/10.5507/fot.2023.001openalex-snapshot
Differences in pigment composition and concentration between phototrophic, mixotrophic, and heterotrophic Chrysophyceae
inferred← citeshttps://doi.org/10.5507/fot.2023.003openalex-snapshot
Effects of stressors on growth and competition between different cryptic taxa affiliated with Ochromonadales (Chrysophyceae)
inferred← citeshttps://doi.org/10.70675/991b1cd3ze91ez432fza67fz14ace1dd2b61openalex-snapshot
Contribution of phototrophic microbes to peatland carbon uptake in a changing climate
inferred← citeshttps://doi.org/10.70675/9b1d2f49z9112z4791z9086zd63cdc0a8296openalex-snapshot
Mixotrophy of photosymbiotic Radiolaria
inferred← citeshttps://doi.org/10.7287/peerj.5894v0.1/reviews/1openalex-snapshot
Peer Review #1 of "Putatively asexual chrysophytes have meiotic genes: evidence from transcriptomic data (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.5894v0.1/reviews/2openalex-snapshot
Peer Review #2 of "Putatively asexual chrysophytes have meiotic genes: evidence from transcriptomic data (v0.1)"
inferred← citeshttps://doi.org/10.7717/peerj.17912openalex-snapshot
Insights from single-strain and mixed culture experiments on the effects of heatwaves on freshwater flagellates
inferred← citeshttps://doi.org/10.7717/peerj.5894openalex-snapshot
Putatively asexual chrysophytes have meiotic genes: evidence from transcriptomic data
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