On the public citation graph

The Paramecium Germline Genome Provides a Niche for Intragenic Parasitic DNA: Evolutionary Dynamics of Internal Eliminated Sequences

0 signed · 268 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.
Claim with ORCID
Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/j.1460-2075.1993.tb05905.xopenalex-snapshot
DNA looping and the helical repeat in vitro and in vivo: effect of HU protein and enhancer location on Hin invertasome assembly.
inferredcites →https://doi.org/10.1006/jmbi.1994.1585openalex-snapshot
Induction of the SOS Response by IS1 Transposase
inferredcites →https://doi.org/10.1006/jmbi.1996.0143openalex-snapshot
Repression oflacPromoter as a Function of Distance, Phase and Quality of an AuxiliarylacOperator
inferredcites →https://doi.org/10.1016/0003-2697(90)90595-zopenalex-snapshot
Molecular cloning: A laboratory manual
inferredcites →https://doi.org/10.1016/0092-8674(84)90236-8openalex-snapshot
DNA elimination in tetrahymena: A developmental process involving extensive breakage and rejoining of DNA at defined sites
inferredcites →https://doi.org/10.1016/0378-1119(93)90226-sopenalex-snapshot
Structures of the Euplotes crassusTec1 and Tec2 elements: identification of putative transposase coding regions
inferredcites →https://doi.org/10.1016/j.cub.2005.07.033openalex-snapshot
Nowa1p and Nowa2p: Novel Putative RNA Binding Proteins Involved in trans-Nuclear Crosstalk in Paramecium tetraurelia
inferredcites →https://doi.org/10.1016/j.resmic.2004.01.017openalex-snapshot
Large-scale genome remodelling by the developmentally programmed elimination of germ line sequences in the ciliate Paramecium
inferredcites →https://doi.org/10.1016/j.resmic.2011.02.012openalex-snapshot
Remembrance of things past retrieved from the Paramecium genome
inferredcites →https://doi.org/10.1016/j.tig.2009.05.007openalex-snapshot
Developmental genome rearrangements in ciliates: a natural genomic subtraction mediated by non-coding transcripts
inferredcites →https://doi.org/10.1016/s0079-6603(08)61001-6openalex-snapshot
Developmental Genome Reorganization in Ciliated Protozoa: The Transposon Link
inferredcites →https://doi.org/10.1016/s0168-9525(01)02548-3openalex-snapshot
RNA interference by feeding in Paramecium
inferredcites →https://doi.org/10.1016/s0168-9525(99)01777-1openalex-snapshot
Resident aliens: the Tc1/ mariner superfamily of transposable elements
inferredcites →https://doi.org/10.1016/s0378-1119(00)00579-5openalex-snapshot
Ingestion of bacterially expressed dsRNAs can produce specific and potent genetic interference in Caenorhabditis elegans
inferredcites →https://doi.org/10.1016/s0960-9822(00)00804-6openalex-snapshot
The SM19 gene, required for duplication of basal bodies in Paramecium, encodes a novel tubulin, η-tubulin
inferredcites →https://doi.org/10.1021/bi00411a002openalex-snapshot
Physical properties of DNA in vivo as probed by the length dependence of the lac operator looping process
inferredcites →https://doi.org/10.1038/27579openalex-snapshot
Specific interference by ingested dsRNA
inferredcites →https://doi.org/10.1038/emboj.2008.41openalex-snapshot
piggyBac can bypass DNA synthesis during cut and paste transposition
inferredcites →https://doi.org/10.1038/nature02874openalex-snapshot
RNA silencing in plants
inferredcites →https://doi.org/10.1038/nature05230openalex-snapshot
Global trends of whole-genome duplications revealed by the ciliate Paramecium tetraurelia
inferredcites →https://doi.org/10.1038/nature06452openalex-snapshot
RNA-mediated epigenetic programming of a genome-rearrangement pathway
inferredcites →https://doi.org/10.1038/nature06495openalex-snapshot
Translational control of intron splicing in eukaryotes
inferredcites →https://doi.org/10.1073/pnas.1102343108openalex-snapshot
Selfish genetic elements, genetic conflict, and evolutionary innovation
inferredcites →https://doi.org/10.1073/pnas.1110633108openalex-snapshot
Estimating the timing of early eukaryotic diversification with multigene molecular clocks
inferredcites →https://doi.org/10.1073/pnas.55.6.1462openalex-snapshot
Assembly of phage lambda in vitro.
inferredcites →https://doi.org/10.1073/pnas.86.2.476openalex-snapshot
In vivo DNA loops in araCBAD: size limits and helical repeat.
inferredcites →https://doi.org/10.1073/pnas.91.23.10834openalex-snapshot
DNA length, bending, and twisting constraints on IS50 transposition.
inferredcites →https://doi.org/10.1073/pnas.91.3.942openalex-snapshot
A proposed superfamily of transposase genes: transposon-like elements in ciliated protozoa and a common "D35E" motif.
inferredcites →https://doi.org/10.1073/pnas.91.6.2255openalex-snapshot
Developmentally excised sequences in micronuclear DNA of Paramecium.
inferredcites →https://doi.org/10.1074/jbc.r111.276964openalex-snapshot
Keeping the Soma Free of Transposons: Programmed DNA Elimination in Ciliates
inferredcites →https://doi.org/10.1078/1434-4610-00084openalex-snapshot
Coding Properties of Macronuclear DNA Molecules in Sterkiella nova (Oxytricha nova)
inferredcites →https://doi.org/10.1091/mbc.e09-12-1079openalex-snapshot
A Domesticated piggyBac Transposase Plays Key Roles in Heterochromatin Dynamics and DNA Cleavage during Programmed DNA Deletion in Tetrahymena thermophila
inferredcites →https://doi.org/10.1093/bioinformatics/btg412openalex-snapshot
APE: Analyses of Phylogenetics and Evolution in R language
inferredcites →https://doi.org/10.1093/bioinformatics/btp324openalex-snapshot
Fast and accurate short read alignment with Burrows–Wheeler transform
inferredcites →https://doi.org/10.1093/bioinformatics/btp352openalex-snapshot
The Sequence Alignment/Map format and SAMtools
inferredcites →https://doi.org/10.1093/emboj/20.12.3251openalex-snapshot
Product analysis illuminates the final steps of IES deletion in Tetrahymena thermophila
inferredcites →https://doi.org/10.1093/genetics/143.1.191openalex-snapshot
A Mendelian Mutation Affecting Mating-Type Determination Also Affects Developmental Genomic Rearrangements in Paramecium tetraurelita
inferredcites →https://doi.org/10.1093/genetics/148.1.139openalex-snapshot
A Mutation in Paramecium tetraurelia Reveals Functional and Structural Features of Developmentally Excised DNA Elements
inferredcites →https://doi.org/10.1093/genetics/151.2.597openalex-snapshot
A Mutation in the Flanking 5′-TA-3′ Dinucleotide Prevents Excision of an Internal Eliminated Sequence From the Paramecium tetraurelia Genome
inferredcites →https://doi.org/10.1093/genetics/155.3.1105openalex-snapshot
The Cloning and Molecular Analysis of pawn-B in Paramecium tetraurelia
inferredcites →https://doi.org/10.1093/molbev/msj050openalex-snapshot
The Origins of Eukaryotic Gene Structure
inferredcites →https://doi.org/10.1093/molbev/msn266openalex-snapshot
Genetic Diversity in the Paramecium aurelia Species Complex
inferredcites →https://doi.org/10.1093/nar/23.11.2006openalex-snapshot
Consensus inverted terminal repeat sequence ofParameciumlESs: resemblance to termini of Tc1 -related andEuplotesTec transposons
inferredcites →https://doi.org/10.1093/nar/25.12.2448openalex-snapshot
Deletion endpoint allele-specificity in the developmentally regulated elimination of an internal sequence (IES) in Paramecium
inferredcites →https://doi.org/10.1093/nar/27.5.1243openalex-snapshot
The evolutionary scrambling and developmental unscrambling of germline genes in hypotrichous ciliates
inferredcites →https://doi.org/10.1093/nar/30.11.2524openalex-snapshot
A novel family of mobile genetic elements is limited to the germline genome in Tetrahymena thermophila
inferredcites →https://doi.org/10.1093/nar/gkae201openalex-snapshot
The diversity of splicing modifiers acting on A-1 bulged 5′-splice sites reveals rules for rational drug design
inferredcites →https://doi.org/10.1093/nar/gkh340openalex-snapshot
MUSCLE: multiple sequence alignment with high accuracy and high throughput
inferredcites →https://doi.org/10.1093/nar/gkn1018openalex-snapshot
Silencing-associated and meiosis-specific small RNA pathways in Paramecium tetraurelia
inferredcites →https://doi.org/10.1093/nar/gkn154openalex-snapshot
Developmentally programmed DNA splicing in Paramecium reveals short-distance crosstalk between DNA cleavage sites
inferredcites →https://doi.org/10.1093/nar/gkq755openalex-snapshot
Gene repression by minimal lac loops in vivo
inferredcites →https://doi.org/10.1093/nar/gkq918openalex-snapshot
ParameciumDB in 2011: new tools and new data for functional and comparative genomics of the model ciliate Paramecium tetraurelia
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a025808openalex-snapshot
BIONJ: an improved version of the NJ algorithm based on a simple model of sequence data
inferredcites →https://doi.org/10.1101/cshperspect.a003616openalex-snapshot
Group II Introns: Mobile Ribozymes that Invade DNA
inferredcites →https://doi.org/10.1101/cshperspect_biol/openalex-snapshot
Cold Spring Harbor Perspectives in Biology
inferredcites →https://doi.org/10.1101/gad.473008openalex-snapshot
Maternal noncoding transcripts antagonize the targeting of DNA elimination by scanRNAs in Paramecium tetraurelia
inferredcites →https://doi.org/10.1101/gad.547309openalex-snapshot
PiggyMac, a domesticated piggyBac transposase involved in programmed genome rearrangements in the ciliate Paramecium tetraurelia
inferredcites →https://doi.org/10.1101/gad.6.2.211openalex-snapshot
Induction of specific macronuclear developmental mutations by microinjection of a cloned telomeric gene in Paramecium primaurelia.
inferredcites →https://doi.org/10.1101/gad.7.1.84openalex-snapshot
Circular forms of developmentally excised DNA in Euplotes crassus have a heteroduplex junction.
inferredcites →https://doi.org/10.1101/gad.7.1.95openalex-snapshot
Elimination of Tec elements involves a novel excision process.
inferredcites →https://doi.org/10.1101/gad.7.8.1521openalex-snapshot
The nonspecific DNA-binding and -bending proteins HMG1 and HMG2 promote the assembly of complex nucleoprotein structures.
inferredcites →https://doi.org/10.1101/gad.9.16.2065openalex-snapshot
Epigenetic self-regulation of developmental excision of an internal eliminated sequence on Paramecium tetraurelia.
inferredcites →https://doi.org/10.1101/gr.074492.107openalex-snapshot
Velvet: Algorithms for de novo short read assembly using de Bruijn graphs
inferredcites →https://doi.org/10.1101/gr.074534.107openalex-snapshot
Analysis of sequence variability in the macronuclear DNA of Paramecium tetraurelia: A somatic view of the germline
inferredcites →https://doi.org/10.1101/gr.083899.108openalex-snapshot
Do genetic recombination and gene density shape the pattern of DNA elimination in rice long terminal repeat retrotransposons?
inferredcites →https://doi.org/10.1101/gr.229202openalex-snapshot
BLAT —The BLAST -Like Alignment Tool
inferredcites →https://doi.org/10.1101/gr.849004openalex-snapshot
WebLogo: A Sequence Logo Generator: Figure 1
inferredcites →https://doi.org/10.1101/sqb.2009.74.052openalex-snapshot
Molecular Evolution of piRNA and Transposon Control Pathways in Drosophila
inferredcites →https://doi.org/10.1111/boc.201100057openalex-snapshot
RNA‐guided DNA rearrangements in ciliates: Is the best genome defence a good offence?
inferredcites →https://doi.org/10.1111/j.1550-7408.1992.tb04448.xopenalex-snapshot
Micronuclear DNA from Paramecium tetraurelia: Serotype 51 A Gene Has Internally Eliminated Sequences
inferredcites →https://doi.org/10.1126/science.1170023openalex-snapshot
A Functional Role for Transposases in a Large Eukaryotic Genome
inferredcites →https://doi.org/10.1126/science.1194776openalex-snapshot
A Small-RNA Perspective on Gametogenesis, Fertilization, and Early Zygotic Development
inferredcites →https://doi.org/10.1126/science.42.1074.161openalex-snapshot
The Proceedings of the National Academy of Sciences
inferredcites →https://doi.org/10.1128/9781555817954.ch15openalex-snapshot
Insertion Sequences Revisited
inferredcites →https://doi.org/10.1128/ec.2.1.103-114.2003openalex-snapshot
Tec3, a New Developmentally Eliminated DNA Element in Euplotes crassus
inferredcites →https://doi.org/10.1128/ec.2.5.1076-1090.2003openalex-snapshot
Developmentally Regulated Chromosome Fragmentation Linked to Imprecise Elimination of Repeated Sequences in Paramecia
inferredcites →https://doi.org/10.1128/ec.3.1.157-169.2004openalex-snapshot
A Non-Long Terminal Repeat Retrotransposon Family Is Restricted to the Germ Line Micronucleus of the Ciliated Protozoan Tetrahymena thermophila
inferredcites →https://doi.org/10.1128/ec.4.10.1613-1619.2005openalex-snapshot
Analysis of Paramecium tetraurelia A-51 Surface Antigen Gene Mutants Reveals Positive-Feedback Mechanisms for Maintenance of Expression and Temperature-Induced Activation
inferredcites →https://doi.org/10.1128/mcb.17.1.326openalex-snapshot
Volatility of Internal Eliminated Segments in Germ Line Genes of Hypotrichous Ciliates
inferredcites →https://doi.org/10.1128/mcb.18.12.7075openalex-snapshot
Homology-Dependent Maternal Inhibition of Developmental Excision of Internal Eliminated Sequences in Paramecium tetraurelia
inferredcites →https://doi.org/10.1128/mcb.20.5.1553-1561.2000openalex-snapshot
Timing of Developmentally Programmed Excision and Circularization of Paramecium Internal Eliminated Sequences
inferredcites →https://doi.org/10.1128/mcb.23.20.7152-7162.2003openalex-snapshot
Processing of Double-Strand Breaks Is Involved in the Precise Excision ofParameciumInternal Eliminated Sequences
inferredcites →https://doi.org/10.1128/mcb.24.17.7370-7379.2004openalex-snapshot
RNA-Mediated Programming of Developmental Genome Rearrangements in Paramecium tetraurelia
inferredcites →https://doi.org/10.1128/mcb.4.8.1583openalex-snapshot
Mendelian and non-mendelian mutations affecting surface antigen expression in Paramecium tetraurelia.
inferredcites →https://doi.org/10.1146/annurev-genet-110410-132432openalex-snapshot
DNA Elimination in Ciliates: Transposon Domestication and Genome Surveillance
inferredcites →https://doi.org/10.1146/annurev.bi.61.070192.001215openalex-snapshot
DNA LOOPING
inferredcites →https://doi.org/10.1146/annurev.genet.39.073003.095906openalex-snapshot
RNA-Guided DNA Deletion in Tetrahymena: An RNAi-Based Mechanism for Programmed Genome Rearrangements
inferredcites →https://doi.org/10.1146/annurev.micro.56.012302.160916openalex-snapshot
Genome Remodeling in Ciliated Protozoa
inferredcites →https://doi.org/10.1186/1471-2164-11-547openalex-snapshot
Gene expression in a paleopolyploid: a transcriptome resource for the ciliate Paramecium tetraurelia
inferredcites →https://doi.org/10.1371/journal.pbio.0040286openalex-snapshot
Macronuclear Genome Sequence of the Ciliate Tetrahymena thermophila, a Model Eukaryote
inferredcites →https://doi.org/10.1371/journal.pgen.1000944openalex-snapshot
The Relationship among Gene Expression, the Evolution of Gene Dosage, and the Rate of Protein Evolution
inferredcites →https://doi.org/10.1371/journal.pgen.1002049openalex-snapshot
Highly Precise and Developmentally Programmed Genome Assembly in Paramecium Requires Ligase IV–Dependent End Joining
inferredcites →https://doi.org/10.1534/g3.111.000927openalex-snapshot
Genome-Scale Analysis of Programmed DNA Elimination Sites in Tetrahymena thermophila
inferredcites →https://doi.org/10.1534/genetics.104.037317openalex-snapshot
Ty1 Copy Number Dynamics in Saccharomyces
inferredcites →https://doi.org/10.32614/r.manualsopenalex-snapshot
R: A Language and Environment for Statistical Computing

What points at this work

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

inferred← citeshttps://doi.org/10.1093/zoolinnean/zlad196zenodo-depositor-declared
An overview of genetic manipulation tools in the studies of ciliates, with emphasis on gene knockout, knockdown, and overexpression
inferred← citeshttps://doi.org/10.1002/9780470015902.a0029300openalex-snapshot
Paramecium
inferred← citeshttps://doi.org/10.1002/9781118647110.ch8openalex-snapshot
RNA ‐Mediated Somatic Genome Rearrangement in Ciliates
inferred← citeshttps://doi.org/10.1002/9781394312467.ch4openalex-snapshot
The Silencing Mechanisms Inhibiting Transposable Element Activity in Somatic and Germ Cells
inferred← citeshttps://doi.org/10.1002/bies.201600125openalex-snapshot
Transposable elements: Self‐seekers of the germline, team‐players of the soma
inferred← citeshttps://doi.org/10.1002/wrna.1293openalex-snapshot
On the path to genetic novelties: insights from programmed DNA elimination and RNA splicing
inferred← citeshttps://doi.org/10.1002/wrna.1848openalex-snapshot
Small‐RNA ‐guided histone modifications and somatic genome elimination in ciliates
inferred← citeshttps://doi.org/10.1007/978-3-030-23459-1_13openalex-snapshot
Paramecium Biology
inferred← citeshttps://doi.org/10.1007/978-3-032-24295-2_11openalex-snapshot
Non-mendelian Inheritance and Evolution in Ciliates with a Focus on Transposons
inferred← citeshttps://doi.org/10.1007/978-3-319-32211-7_11openalex-snapshot
Communication in Tetrahymena Reproduction
inferred← citeshttps://doi.org/10.1007/978-3-319-32211-7_3openalex-snapshot
RNA-Guided Genome Editing
inferred← citeshttps://doi.org/10.1007/978-3-642-40193-0_12openalex-snapshot
Programmed Genome Processing in Ciliates
inferred← citeshttps://doi.org/10.1007/s00018-020-03555-2openalex-snapshot
Programmed genome rearrangements in ciliates
inferred← citeshttps://doi.org/10.1007/s00412-017-0655-4openalex-snapshot
RNA-mediated transgenerational inheritance in ciliates and plants
inferred← citeshttps://doi.org/10.1007/s11427-018-9333-1openalex-snapshot
A paradox: rapid evolution rates of germline-limited sequences are associated with conserved patterns of rearrangements in cryptic species of Chilodonella uncinata (Protista, Ciliophora)
inferred← citeshttps://doi.org/10.1007/s11427-023-2605-9openalex-snapshot
Genes and proteins expressed at different life cycle stages in the model protist Euplotes vannus revealed by both transcriptomic and proteomic approaches
inferred← citeshttps://doi.org/10.1007/s42995-023-00213-xopenalex-snapshot
From germline genome to highly fragmented somatic genome: genome-wide DNA rearrangement during the sexual process in ciliated protists
inferred← citeshttps://doi.org/10.1016/b978-0-12-800255-1.00003-xopenalex-snapshot
Unicellular Eukaryotes as Models in Cell and Molecular Biology
inferred← citeshttps://doi.org/10.1016/b978-0-12-809633-8.20894-7openalex-snapshot
Paramecium Molecular Evolution
inferred← citeshttps://doi.org/10.1016/b978-0-12-822563-9.00141-4openalex-snapshot
Paramecium Molecular Evolution
inferred← citeshttps://doi.org/10.1016/bs.mie.2018.08.012openalex-snapshot
The Challenges of Genome-Wide Studies in a Unicellular Eukaryote With Two Nuclear Genomes
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2022.119239openalex-snapshot
Early developmental, meiosis-specific proteins — Spo11, Msh4-1, and Msh5 — Affect subsequent genome reorganization in Paramecium tetraurelia
inferred← citeshttps://doi.org/10.1016/j.cell.2012.10.045openalex-snapshot
Piwi-Interacting RNAs Protect DNA against Loss during Oxytricha Genome Rearrangement
inferred← citeshttps://doi.org/10.1016/j.cell.2013.01.005openalex-snapshot
Genomes on the Edge: Programmed Genome Instability in Ciliates
inferred← citeshttps://doi.org/10.1016/j.cell.2014.07.034openalex-snapshot
The Architecture of a Scrambled Genome Reveals Massive Levels of Genomic Rearrangement during Development
inferred← citeshttps://doi.org/10.1016/j.cell.2017.02.020openalex-snapshot
Circular Concatemers of Ultra-Short DNA Segments Produce Regulatory RNAs
inferred← citeshttps://doi.org/10.1016/j.cell.2018.02.029openalex-snapshot
Dicer-like Enzymes with Sequence Cleavage Preferences
inferred← citeshttps://doi.org/10.1016/j.celrep.2017.06.050openalex-snapshot
Two Sets of Piwi Proteins Are Involved in Distinct sRNA Pathways Leading to Elimination of Germline-Specific DNA
inferred← citeshttps://doi.org/10.1016/j.celrep.2022.111263openalex-snapshot
A small RNA-guided PRC2 complex eliminates DNA as an extreme form of transposon silencing
inferred← citeshttps://doi.org/10.1016/j.celrep.2024.114001openalex-snapshot
Uncoupling programmed DNA cleavage and repair scrambles the Paramecium somatic genome
inferred← citeshttps://doi.org/10.1016/j.cub.2018.04.071openalex-snapshot
Small RNA-Mediated trans-Nuclear and trans-Element Communications in Tetrahymena DNA Elimination
inferred← citeshttps://doi.org/10.1016/j.devcel.2013.12.010openalex-snapshot
Functional Diversification of Dicer-like Proteins and Small RNAs Required for Genome Sculpting
inferred← citeshttps://doi.org/10.1016/j.devcel.2022.03.014openalex-snapshot
Paramecium Polycomb repressive complex 2 physically interacts with the small RNA-binding PIWI protein to repress transposable elements
inferred← citeshttps://doi.org/10.1016/j.dnarep.2019.03.011openalex-snapshot
Identification of a miniature Sae2/Ctp1/CtIP ortholog from Paramecium tetraurelia required for sexual reproduction and DNA double-strand break repair
inferred← citeshttps://doi.org/10.1016/j.ejop.2017.05.004openalex-snapshot
Insights into transgenerational epigenetics from studies of ciliates
inferred← citeshttps://doi.org/10.1016/j.ejop.2017.06.006openalex-snapshot
A comparative study of genome organization and epigenetic mechanisms in model ciliates, with an emphasis on Tetrahymena , Paramecium and Oxytricha
inferred← citeshttps://doi.org/10.1016/j.ejop.2021.125840openalex-snapshot
DAPI staining and DNA content estimation of nuclei in uncultivable microbial eukaryotes (Arcellinida and Ciliates)
inferred← citeshttps://doi.org/10.1016/j.jgg.2026.09.011openalex-snapshot
Transcriptional reprogramming and epigenetic regulation in Paramecium caudatum: a new model for studying extreme germline DNA elimination
inferred← citeshttps://doi.org/10.1016/j.jmb.2019.12.042openalex-snapshot
Roles of Noncoding RNAs in Ciliate Genome Architecture
inferred← citeshttps://doi.org/10.1016/j.molcel.2015.05.024openalex-snapshot
Small-RNA-Mediated Genome-wide trans -Recognition Network in Tetrahymena DNA Elimination
inferred← citeshttps://doi.org/10.1016/j.tcb.2019.11.005openalex-snapshot
Coupling DNA Damage and Repair: an Essential Safeguard during Programmed DNA Double-Strand Breaks?
inferred← citeshttps://doi.org/10.1016/j.tig.2017.01.005openalex-snapshot
Necessity Is the Mother of Invention: Ciliates, Transposons, and Transgenerational Inheritance
inferred← citeshttps://doi.org/10.1016/j.tig.2017.07.011openalex-snapshot
Transposable Element Domestication As an Adaptation to Evolutionary Conflicts
inferred← citeshttps://doi.org/10.1016/j.tig.2023.02.016openalex-snapshot
When cleaning facilitates cluttering – genome editing in ciliates
inferred← citeshttps://doi.org/10.1038/nature13318openalex-snapshot
Genome-defence small RNAs exapted for epigenetic mating-type inheritance
inferred← citeshttps://doi.org/10.1038/nature13333openalex-snapshot
Keeping one's sex
inferred← citeshttps://doi.org/10.1038/s41467-019-10648-5openalex-snapshot
The Polycomb protein Ezl1 mediates H3K9 and H3K27 methylation to repress transposable elements in Paramecium
inferred← citeshttps://doi.org/10.1038/s41576-026-01004-7openalex-snapshot
The mechanistic and evolutionary diversity of programmed DNA elimination
inferred← citeshttps://doi.org/10.1038/s44318-026-00795-zopenalex-snapshot
Host-transposable element coexistence: a matter of resistance, tolerance and trade-off
inferred← citeshttps://doi.org/10.1038/s44319-024-00332-1openalex-snapshot
Heterochromatin-dependent transcription links the PRC2 complex to small RNA-mediated DNA elimination
inferred← citeshttps://doi.org/10.1042/bst20253006openalex-snapshot
Functions and mechanisms of eukaryotic RNA-guided programmed DNA elimination
inferred← citeshttps://doi.org/10.1073/pnas.2213887120openalex-snapshot
Origins of genome-editing excisases as illuminated by the somatic genome of the ciliate Blepharisma
inferred← citeshttps://doi.org/10.1073/pnas.2213985120openalex-snapshot
MITE infestation accommodated by genome editing in the germline genome of the ciliate Blepharisma
inferred← citeshttps://doi.org/10.1073/pnas.2221818120openalex-snapshot
How ciliates got their nuclei
inferred← citeshttps://doi.org/10.1073/pnas.2400503121openalex-snapshot
Nuclear dualism without extensive DNA elimination in the ciliate Loxodes magnus
inferred← citeshttps://doi.org/10.1093/bioinformatics/btab613openalex-snapshot
BleTIES: annotation of natural genome editing in ciliates using long read sequencing
inferred← citeshttps://doi.org/10.1093/bioinformatics/btv691openalex-snapshot
ParTIES: a toolbox for Paramecium interspersed DNA elimination studies
inferred← citeshttps://doi.org/10.1093/femsle/fnaf088openalex-snapshot
Golgi_traff phylogeny reveals ancient eukaryotic genes with recent surprises: replication and diversification of HID1 domain-containing protein unique to Schizosaccharomyces
inferred← citeshttps://doi.org/10.1093/gbe/evaa147openalex-snapshot
SIGAR: Inferring Features of Genome Architecture and DNA Rearrangements by Split-Read Mapping
inferred← citeshttps://doi.org/10.1093/gbe/evaa258openalex-snapshot
Evolutionary Plasticity of Mating-Type Determination Mechanisms in Paramecium aurelia Sibling Species
inferred← citeshttps://doi.org/10.1093/gbe/evab263openalex-snapshot
One Cell, Two Gears: Extensive Somatic Genome Plasticity Accompanies High Germline Genome Stability in Paramecium
inferred← citeshttps://doi.org/10.1093/gbe/evt087openalex-snapshot
Spliced DNA Sequences in the Paramecium Germline: Their Properties and Evolutionary Potential
inferred← citeshttps://doi.org/10.1093/gbe/evy055openalex-snapshot
Insights into an Extensively Fragmented Eukaryotic Genome: De Novo Genome Sequencing of the Multinuclear Ciliate Uroleptopsis citrina
inferred← citeshttps://doi.org/10.1093/gbe/evy133openalex-snapshot
Twisted Tales: Insights into Genome Diversity of Ciliates Using Single-Cell ‘Omics
inferred← citeshttps://doi.org/10.1093/molbev/msad107openalex-snapshot
Dynamics of Gene Loss following Ancient Whole-Genome Duplication in the Cryptic Paramecium Complex
inferred← citeshttps://doi.org/10.1093/molbev/msx074openalex-snapshot
Population Genomics of Paramecium Species
inferred← citeshttps://doi.org/10.1093/nar/gkaa472openalex-snapshot
A universal method for the rapid isolation of all known classes of functional silencing small RNAs
inferred← citeshttps://doi.org/10.1093/nar/gkac106openalex-snapshot
The transient Spt4-Spt5 complex as an upstream regulator of non-coding RNAs during development
inferred← citeshttps://doi.org/10.1093/nar/gkad1006openalex-snapshot
Inter-generational nuclear crosstalk links the control of gene expression to programmed genome rearrangement during the Paramecium sexual cycle
inferred← citeshttps://doi.org/10.1093/nar/gkae1055openalex-snapshot
The PIWI-interacting protein Gtsf1 controls the selective degradation of small RNAs in Paramecium
inferred← citeshttps://doi.org/10.1093/nar/gkae925openalex-snapshot
GTSF1 is required for transposon silencing in the unicellular eukaryote Paramecium tetraurelia
inferred← citeshttps://doi.org/10.1093/nar/gkaf1048openalex-snapshot
A histone methyltransferase-independent function of PRC2 controls small RNA dynamics during programmed DNA elimination in Paramecium
inferred← citeshttps://doi.org/10.1093/nar/gkaf286openalex-snapshot
The linker region of a development-specific DNA polymerase X ensures efficient repair of programmed DNA double-strand breaks in Paramecium tetraurelia
inferred← citeshttps://doi.org/10.1093/nar/gkaf577openalex-snapshot
Relaxed DNA substrate specificity of transposases involved in programmed genome rearrangement
inferred← citeshttps://doi.org/10.1093/nar/gku1331openalex-snapshot
Primary and secondary siRNA synthesis triggered by RNAs from food bacteria in the ciliate Paramecium tetraurelia
inferred← citeshttps://doi.org/10.1093/nar/gku223openalex-snapshot
A forward genetic screen reveals essential and non-essential RNAi factors in Paramecium tetraurelia
inferred← citeshttps://doi.org/10.1093/nar/gku619openalex-snapshot
Genome-wide analysis of genetic and epigenetic control of programmed DNA deletion
inferred← citeshttps://doi.org/10.1093/nar/gku874openalex-snapshot
Paramecium tetraurelia chromatin assembly factor-1-like protein PtCAF-1 is involved in RNA-mediated control of DNA elimination
inferred← citeshttps://doi.org/10.1093/nar/gkv1110openalex-snapshot
DNA deletion as a mechanism for developmentally programmed centromere loss
inferred← citeshttps://doi.org/10.1093/nar/gkv843openalex-snapshot
Cis-acting signals modulate the efficiency of programmed DNA elimination inParamecium tetraurelia
inferred← citeshttps://doi.org/10.1093/nar/gkw1318openalex-snapshot
A meiosis-specific Spt5 homolog involved in non-coding transcription
inferred← citeshttps://doi.org/10.1093/nar/gkw1359openalex-snapshot
Multimerization properties of PiggyMac, a domesticatedpiggyBactransposase involved in programmed genome rearrangements
inferred← citeshttps://doi.org/10.1093/nar/gkx652openalex-snapshot
A germline-limited piggyBac transposase gene is required for precise excision in Tetrahymena genome rearrangement
inferred← citeshttps://doi.org/10.1093/nar/gky772openalex-snapshot
A mating-type mutagenesis screen identifies a zinc-finger protein required for specific DNA excision events in Paramecium
inferred← citeshttps://doi.org/10.1093/nar/gkz725openalex-snapshot
Programmed genome rearrangements in Oxytricha produce transcriptionally active extrachromosomal circular DNA
inferred← citeshttps://doi.org/10.1093/nar/gkz948openalex-snapshot
ParameciumDB 2019: integrating genomic data across the genus for functional and evolutionary biology
inferred← citeshttps://doi.org/10.1098/rsob.170172openalex-snapshot
Whats, hows and whys of programmed DNA elimination inTetrahymena
inferred← citeshttps://doi.org/10.1101/2020.04.07.030270openalex-snapshot
Prolonged exposure to constant environmental conditions prompts nonrandom genetic variation
inferred← citeshttps://doi.org/10.1101/2021.08.12.456067openalex-snapshot
Paramecium Polycomb Repressive Complex 2 physically interacts with the small RNA binding PIWI protein to repress transposable elements
inferred← citeshttps://doi.org/10.1101/2021.12.14.471607openalex-snapshot
Genome editing excisase origins illuminated by somatic genome of Blepharisma
inferred← citeshttps://doi.org/10.1101/2022.05.02.489906openalex-snapshot
MITE infestation of germline accommodated by genome editing in Blepharisma
inferred← citeshttps://doi.org/10.1101/2023.10.06.561219openalex-snapshot
Conservation of the ancestral function of GTSF1 in transposon silencing in the unicellular eukaryote Paramecium tetraurelia
inferred← citeshttps://doi.org/10.1101/2024.01.23.576875openalex-snapshot
Two paralogous PHD finger proteins participate in Paramecium tetraurelia ’s natural genome editing
inferred← citeshttps://doi.org/10.1101/2024.07.18.604053openalex-snapshot
A development-specific POLX essential for programmed genome rearrangement in Paramecium tetraurelia
inferred← citeshttps://doi.org/10.1101/2024.07.26.605286openalex-snapshot
Mechanisms Ensuring Fidelity of Family X DNA Polymerases in Programmed DNA rearrangements in Paramecium tetraurelia
inferred← citeshttps://doi.org/10.1101/2024.08.09.607295openalex-snapshot
De novo genome sequence assembly of the RNAi-tractable endosymbiosis model system Paramecium bursaria 186b reveals factors shaping intron repertoire
inferred← citeshttps://doi.org/10.1101/2025.08.21.671558openalex-snapshot
Somatic Programmed DNA Elimination is widespread in free-living Rhabditidae nematodes
inferred← citeshttps://doi.org/10.1101/448316openalex-snapshot
Enhanced plasticity of programmed DNA elimination boosts adaptive potential in suboptimal environments
inferred← citeshttps://doi.org/10.1101/cshperspect.a017764openalex-snapshot
Epigenetics of Ciliates
inferred← citeshttps://doi.org/10.1101/gad.320796.118openalex-snapshot
RNAi-dependent Polycomb repression controls transposable elements in Tetrahymena
inferred← citeshttps://doi.org/10.1101/gr.245332.118openalex-snapshot
Environmentally induced plasticity of programmed DNA elimination boosts somatic variability in Paramecium tetraurelia
inferred← citeshttps://doi.org/10.1101/gr.276125.121openalex-snapshot
GC content, but not nucleosome positioning, directly contributes to intron splicing efficiency in Paramecium
inferred← citeshttps://doi.org/10.1101/gr.276126.121openalex-snapshot
Broad domains of histone marks in the highly compact Paramecium macronuclear genome
inferred← citeshttps://doi.org/10.1101/gr.277027.122openalex-snapshot
Developmental timing of programmed DNA elimination in Paramecium tetraurelia recapitulates germline transposon evolutionary dynamics
inferred← citeshttps://doi.org/10.1101/gr.278402.123openalex-snapshot
ISWI1 complex proteins facilitate developmental genome editing in Paramecium
inferred← citeshttps://doi.org/10.1111/jeu.12891openalex-snapshot
Epigenetic influences of mobile genetic elements on ciliate genome architecture and evolution
inferred← citeshttps://doi.org/10.1111/jeu.12898openalex-snapshot
Macronuclear development in ciliates, with a focus on nuclear architecture
inferred← citeshttps://doi.org/10.1111/jeu.12914openalex-snapshot
Paramecium epigenetics in development and proliferation
inferred← citeshttps://doi.org/10.1111/jeu.12926openalex-snapshot
Ciliate research: From myth to trendsetting science
inferred← citeshttps://doi.org/10.1111/nyas.12636openalex-snapshot
The eukaryotic way to defend and edit genomes by sRNA‐targeted DNA deletion
inferred← citeshttps://doi.org/10.1111/nyas.14108openalex-snapshot
Evolutionary origins and impacts of genome architecture in ciliates
inferred← citeshttps://doi.org/10.1126/sciadv.adx3690openalex-snapshot
Soma-derived 30-nt small RNAs are coupled with chromosome breakage and precisely target nontransposon DNA against elimination in Euplotes vannus
inferred← citeshttps://doi.org/10.1128/9781555819217.ch17openalex-snapshot
Programmed Rearrangement in Ciliates: Paramecium
inferred← citeshttps://doi.org/10.1128/9781555819217.ch18openalex-snapshot
Programmed Genome Rearrangements in the Ciliate Oxytricha
inferred← citeshttps://doi.org/10.1128/9781555819217.ch34openalex-snapshot
Mariner and the ITm Superfamily of Transposons
inferred← citeshttps://doi.org/10.1128/mbio.01328-14openalex-snapshot
Genomic Characterization of Variable Surface Antigens Reveals a Telomere Position Effect as a Prerequisite for RNA Interference-Mediated Silencing in Paramecium tetraurelia
inferred← citeshttps://doi.org/10.1128/mbio.01836-17openalex-snapshot
Exploration of the Germline Genome of the Ciliate Chilodonella uncinata through Single-Cell Omics (Transcriptomics and Genomics)
inferred← citeshttps://doi.org/10.1128/microbiolspec.mdna3-0025-2014openalex-snapshot
Programmed Genome Rearrangements in the CiliateOxytricha
inferred← citeshttps://doi.org/10.1128/microbiolspec.mdna3-0033-2014openalex-snapshot
Mariner and the ITm Superfamily of Transposons
inferred← citeshttps://doi.org/10.1128/microbiolspec.mdna3-0035-2014openalex-snapshot
Programmed Rearrangement in Ciliates: Paramecium
inferred← citeshttps://doi.org/10.1128/mmbr.00184-22openalex-snapshot
Programmed chromosome fragmentation in ciliated protozoa: multiple means to chromosome ends
inferred← citeshttps://doi.org/10.1146/annurev-genet-071819-104035openalex-snapshot
Paramecium Genetics, Genomics, and Evolution
inferred← citeshttps://doi.org/10.1146/annurev-micro-090816-093342openalex-snapshot
Genetics and Epigenetics of Mating Type Determination in Paramecium and Tetrahymena
inferred← citeshttps://doi.org/10.1146/annurev-micro-102215-095448openalex-snapshot
Protists and the Wild, Wild West of Gene Expression: New Frontiers, Lawlessness, and Misfits
inferred← citeshttps://doi.org/10.1155/2012/436196openalex-snapshot
Transposon Invasion of theParameciumGermline Genome Countered by a Domesticated PiggyBac Transposase and the NHEJ Pathway
inferred← citeshttps://doi.org/10.1186/1471-2164-15-186openalex-snapshot
Billions of basepairs of recently expanded, repetitive sequences are eliminated from the somatic genome during copepod development
inferred← citeshttps://doi.org/10.1186/s12864-017-3713-7openalex-snapshot
Flow cytometry sorting of nuclei enables the first global characterization of Paramecium germline DNA and transposable elements
inferred← citeshttps://doi.org/10.1186/s12864-017-3887-zopenalex-snapshot
Improved methods and resources for paramecium genomics: transcription units, gene annotation and gene expression
inferred← citeshttps://doi.org/10.1186/s12915-020-00912-2openalex-snapshot
Genome plasticity in Paramecium bursaria revealed by population genomics
inferred← citeshttps://doi.org/10.1186/s13059-026-04045-7openalex-snapshot
A H3K27me3 reader complex couples H3K27me3 accumulation to nascent transcription of transposable elements in Paramecium
inferred← citeshttps://doi.org/10.1186/s13100-016-0057-9openalex-snapshot
Phylogenomic analysis reveals genome-wide purifying selection on TBE transposons in the ciliate Oxytricha
inferred← citeshttps://doi.org/10.1186/s13100-021-00240-4openalex-snapshot
The unusual structure of the PiggyMac cysteine-rich domain reveals zinc finger diversity in PiggyBac-related transposases
inferred← citeshttps://doi.org/10.1242/jcs.261979openalex-snapshot
Two paralogous PHD finger proteins participate in natural genome editing in Paramecium tetraurelia
inferred← citeshttps://doi.org/10.1261/rna.079134.122openalex-snapshot
Identification of novel, functional, long noncoding RNAs involved in programmed, large-scale genome rearrangements
inferred← citeshttps://doi.org/10.12688/f1000research.12121.1openalex-snapshot
Identification and analysis of functional associations among natural eukaryotic genome editing components
inferred← citeshttps://doi.org/10.1371/journal.pbio.1001473openalex-snapshot
The Oxytricha trifallax Macronuclear Genome: A Complex Eukaryotic Genome with 16,000 Tiny Chromosomes
inferred← citeshttps://doi.org/10.1371/journal.pbio.3001309openalex-snapshot
Massive colonization of protein-coding exons by selfish genetic elements in Paramecium germline genomes
inferred← citeshttps://doi.org/10.1371/journal.pbio.3001559openalex-snapshot
Gene-rich germline-restricted chromosomes in black-winged fungus gnats evolved through hybridization
inferred← citeshttps://doi.org/10.1371/journal.pgen.1003659openalex-snapshot
Transposon Domestication versus Mutualism in Ciliate Genome Rearrangements
inferred← citeshttps://doi.org/10.1371/journal.pgen.1004032openalex-snapshot
A Domesticated PiggyBac Transposase Interacts with Heterochromatin and Catalyzes Reproducible DNA Elimination in Tetrahymena
inferred← citeshttps://doi.org/10.1371/journal.pgen.1004086openalex-snapshot
Is Non-Homologous End-Joining Really an Inherently Error-Prone Process?
inferred← citeshttps://doi.org/10.1371/journal.pgen.1004552openalex-snapshot
Ku-Mediated Coupling of DNA Cleavage and Repair during Programmed Genome Rearrangements in the Ciliate Paramecium tetraurelia
inferred← citeshttps://doi.org/10.1371/journal.pgen.1004665openalex-snapshot
Local Effect of Enhancer of Zeste-Like Reveals Cooperation of Epigenetic and cis-Acting Determinants for Zygotic Genome Rearrangements
inferred← citeshttps://doi.org/10.1371/journal.pgen.1005383openalex-snapshot
TFIIS-Dependent Non-coding Transcription Regulates Developmental Genome Rearrangements
inferred← citeshttps://doi.org/10.1371/journal.pgen.1005842openalex-snapshot
A Parallel G Quadruplex-Binding Protein Regulates the Boundaries of DNA Elimination Events of Tetrahymena thermophila
inferred← citeshttps://doi.org/10.1371/journal.pgen.1008723openalex-snapshot
Functional diversification of Paramecium Ku80 paralogs safeguards genome integrity during precise programmed DNA elimination
inferred← citeshttps://doi.org/10.1371/journal.pgen.1008949openalex-snapshot
The Paramecium histone chaperone Spt16-1 is required for Pgm endonuclease function in programmed genome rearrangements
inferred← citeshttps://doi.org/10.1371/journal.pgen.1010913openalex-snapshot
Identification of a non-canonical ciliate nuclear genetic code where UAA and UAG code for different amino acids
inferred← citeshttps://doi.org/10.1371/journal.pone.0112899openalex-snapshot
Pdsg1 and Pdsg2, Novel Proteins Involved in Developmental Genome Remodelling in Paramecium
inferred← citeshttps://doi.org/10.1371/journal.pone.0161476openalex-snapshot
Evolution of the Exon-Intron Structure in Ciliate Genomes
inferred← citeshttps://doi.org/10.1371/journal.pone.0206667openalex-snapshot
Determination of the presence of 5-methylcytosine in Paramecium tetraurelia
inferred← citeshttps://doi.org/10.15252/embj.2022111839openalex-snapshot
Chromatin remodeling is required for sRNA‐guided DNA elimination in Paramecium
inferred← citeshttps://doi.org/10.1534/genetics.114.163287openalex-snapshot
Insights into Three Whole-Genome Duplications Gleaned from theParamecium caudatumGenome Sequence
inferred← citeshttps://doi.org/10.17816/ecogen1645-22openalex-snapshot
RNA interference in formation of the somatic genome of ciliates Paramecium and Tetrahymena
inferred← citeshttps://doi.org/10.21203/rs.3.rs-9235884/v1openalex-snapshot
N6-methyldeoxyadenosine is a transgenerational epigenetic mark protecting DNA from deletion
inferred← citeshttps://doi.org/10.26508/lsa.202302281openalex-snapshot
Structural maintenance of chromosomes (SMC) proteins are required for DNA elimination in Paramecium
inferred← citeshttps://doi.org/10.3389/fcell.2020.584219openalex-snapshot
Cross-Generational Effects and Non-random Developmental Response to Temperature Variation in Paramecium
inferred← citeshttps://doi.org/10.3390/biom11040550openalex-snapshot
The Role of RNA in DNA Breaks, Repair and Chromosomal Rearrangements
inferred← citeshttps://doi.org/10.3390/microorganisms10101901openalex-snapshot
Intronization Signatures in Coding Exons Reveal the Evolutionary Fluidity of Eukaryotic Gene Architecture
inferred← citeshttps://doi.org/10.3390/microorganisms11020418openalex-snapshot
The Conjusome—A Transient Organelle Linking Genome Rearrangements in the Parental and Developing Macronuclei
inferred← citeshttps://doi.org/10.3390/microorganisms11040937openalex-snapshot
A Review for the Special Issue on Paramecium as a Modern Model Organism
inferred← citeshttps://doi.org/10.3390/microorganisms9091979openalex-snapshot
Fifty Generations of Amitosis: Tracing Asymmetric Allele Segregation in Polyploid Cells with Single-Cell DNA Sequencing
inferred← citeshttps://doi.org/10.6084/m9.figshare.13300174openalex-snapshot
Additional file 1 of Genome plasticity in Paramecium bursaria revealed by population genomics
inferred← citeshttps://doi.org/10.6084/m9.figshare.13300177openalex-snapshot
Additional file 2 of Genome plasticity in Paramecium bursaria revealed by population genomics
inferred← citeshttps://doi.org/10.64898/2026.02.13.705781openalex-snapshot
N6-methyldeoxyadenosine is a transgenerational epigenetic mark protecting DNA from deletion
inferred← citeshttps://doi.org/10.70675/13d9e13dz688ez408bza9d1zc1969e4eb7ccopenalex-snapshot
Ciblage & élimination des transposons et de leurs vestiges lors des réarrangements programmés du génome somatique de la paramécie
inferred← citeshttps://doi.org/10.70675/60e0aaadz31f3z4873z8fafz9d3e86686fccopenalex-snapshot
Spécialisation de Ku80c dans le couplage entre coupure et réparation de l’ADN lors des réarrangements programmés du génome chez Paramecium tetraurelia
inferred← citeshttps://doi.org/10.70675/cef4bacezab19z4a37za5e5z90809f6d6f7eopenalex-snapshot
Annotation des génomes de paramécies
inferred← citeshttps://doi.org/10.70675/eaa802d4zd1c0z4a58z9fbez158d83bd3398openalex-snapshot
Élimination programmée d'ADN chez Paramecium tetraurelia : caractérisation de protéines contrôlant la dynamique des petits ARN
inferred← citeshttps://doi.org/10.7554/elife.19090openalex-snapshot
Structure of the germline genome of Tetrahymena thermophila and relationship to the massively rearranged somatic genome
inferred← citeshttps://doi.org/10.7554/elife.23447openalex-snapshot
One genome’s junk is another’s garbage
inferred← citeshttps://doi.org/10.7554/elife.37927openalex-snapshot
Six domesticated PiggyBac transposases together carry out programmed DNA elimination in Paramecium
inferred← citeshttps://doi.org/10.7554/elife.82979openalex-snapshot
Comparative genomics reveals insight into the evolutionary origin of massively scrambled genomes
Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.