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Cicada endosymbionts contain tRNAs that are processed despite having genomes that lack tRNA processing activities
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/j.1460-2075.1987.tb02528.xopenalex-snapshot
tRNA nucleotidyltransferase is not essential for Escherichia coli viability.
inferredcites →https://doi.org/10.1002/wrna.1144openalex-snapshot
Transfer RNA modifications: nature's combinatorial chemistry playground
inferredcites →https://doi.org/10.1006/bbrc.2001.5303openalex-snapshot
The Chloroplast-Derived trnW and trnM-e Genes Are Not Expressed in Arabidopsis Mitochondria
inferredcites →https://doi.org/10.1007/4735_2007_0223openalex-snapshot
Structure, function, and inheritance of plastid genomes
inferredcites →https://doi.org/10.1007/978-3-540-75376-6openalex-snapshot
Cell and Molecular Biology of Plastids
inferredcites →https://doi.org/10.1007/s00239-011-9470-3openalex-snapshot
Unassigned Codons, Nonsense Suppression, and Anticodon Modifications in the Evolution of the Genetic Code
inferredcites →https://doi.org/10.1007/s00294-008-0223-9openalex-snapshot
Import of tRNAs and aminoacyl-tRNA synthetases into mitochondria
inferredcites →https://doi.org/10.1016/0092-8674(83)90117-4openalex-snapshot
The RNA moiety of ribonuclease P is the catalytic subunit of the enzyme
inferredcites →https://doi.org/10.1016/j.ceb.2016.05.008openalex-snapshot
From microbiology to cell biology: when an intracellular bacterium becomes part of its host cell
inferredcites →https://doi.org/10.1016/j.cell.2009.07.001openalex-snapshot
Stressing Out over tRNA Cleavage
inferredcites →https://doi.org/10.1016/j.cell.2013.05.040openalex-snapshot
Horizontal Gene Transfer from Diverse Bacteria to an Insect Genome Enables a Tripartite Nested Mealybug Symbiosis
inferredcites →https://doi.org/10.1016/j.cub.2011.06.051openalex-snapshot
An Interdependent Metabolic Patchwork in the Nested Symbiosis of Mealybugs
inferredcites →https://doi.org/10.1016/j.cub.2014.06.038openalex-snapshot
Aphid gene of bacterial origin encodes a protein transported to an obligate endosymbiont
inferredcites →https://doi.org/10.1016/j.cub.2017.08.010openalex-snapshot
Massive Protein Import into the Early-Evolutionary-Stage Photosynthetic Organelle of the Amoeba Paulinella chromatophora
inferredcites →https://doi.org/10.1016/j.cub.2017.10.008openalex-snapshot
Idiosyncratic Genome Degradation in a Bacterial Endosymbiont of Periodical Cicadas
inferredcites →https://doi.org/10.1016/j.mib.2007.05.008openalex-snapshot
Maturation and degradation of RNA in bacteria
inferredcites →https://doi.org/10.1016/j.mib.2009.12.002openalex-snapshot
The bacterial essence of tiny symbiont genomes
inferredcites →https://doi.org/10.1016/j.tibs.2006.04.007openalex-snapshot
RNase P: interface of the RNA and protein worlds
inferredcites →https://doi.org/10.1016/j.tibs.2008.04.010openalex-snapshot
Recent advances in tRNA mitochondrial import
inferredcites →https://doi.org/10.1016/s0021-9258(17)30645-2openalex-snapshot
The mitochondrial tRNAs of Trypanosoma brucei are nuclear encoded.
inferredcites →https://doi.org/10.1016/s0079-6603(08)60628-5openalex-snapshot
Ribonucleases, ?RNA Nucleotidyltransferase, and the 3' Processing of ?RNA
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/nmeth.3478openalex-snapshot
Efficient and quantitative high-throughput tRNA sequencing
inferredcites →https://doi.org/10.1038/nmeth.3508openalex-snapshot
ARM-seq: AlkB-facilitated RNA methylation sequencing reveals a complex landscape of modified tRNA fragments
inferredcites →https://doi.org/10.1038/nrg1271openalex-snapshot
Endosymbiotic gene transfer: organelle genomes forge eukaryotic chromosomes
inferredcites →https://doi.org/10.1038/nrg2798openalex-snapshot
Evolutionary microbial genomics: insights into bacterial host adaptation
inferredcites →https://doi.org/10.1038/nrmicro2670openalex-snapshot
Extreme genome reduction in symbiotic bacteria
inferredcites →https://doi.org/10.1073/pnas.082682699openalex-snapshot
A Los1p-independent pathway for nuclear export of intronless tRNAs in Saccharomyces cerevisiae
inferredcites →https://doi.org/10.1073/pnas.1118800109openalex-snapshot
Trafficking of protein into the recently established photosynthetic organelles of Paulinella chromatophora
inferredcites →https://doi.org/10.1073/pnas.1421385112openalex-snapshot
Endosymbiotic gene transfer from prokaryotic pangenomes: Inherited chimerism in eukaryotes
inferredcites →https://doi.org/10.1073/pnas.1603910113openalex-snapshot
Repeated replacement of an intrabacterial symbiont in the tripartite nested mealybug symbiosis
inferredcites →https://doi.org/10.1073/pnas.1608016113openalex-snapshot
Gene transfers from diverse bacteria compensate for reductive genome evolution in the chromatophore of Paulinella chromatophora
inferredcites →https://doi.org/10.1073/pnas.1712321115openalex-snapshot
Multiple origins of interdependent endosymbiotic complexes in a genus of cicadas
inferredcites →https://doi.org/10.1073/pnas.1803245115openalex-snapshot
Recurrent symbiont recruitment from fungal parasites in cicadas
inferredcites →https://doi.org/10.1073/pnas.84.5.1324openalex-snapshot
Bizarre tRNAs inferred from DNA sequences of mitochondrial genomes of nematode worms.
inferredcites →https://doi.org/10.1073/pnas.97.14.7778openalex-snapshot
tmRNAs that encode proteolysis-inducing tags are found in all known bacterial genomes: A two-piece tmRNA functions in Caulobacter
inferredcites →https://doi.org/10.1074/jbc.m106202200openalex-snapshot
Identification and Characterization of Mammalian Mitochondrial tRNA nucleotidyltransferases
inferredcites →https://doi.org/10.1074/jbc.m404519200openalex-snapshot
Mitochondrial tRNA Import in Toxoplasma gondii
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/btp616openalex-snapshot
edgeR : a Bioconductor package for differential expression analysis of digital gene expression data
inferredcites →https://doi.org/10.1093/gbe/evt008openalex-snapshot
Strikingly Bacteria-Like and Gene-Rich Mitochondrial Genomes throughout Jakobid Protists
inferredcites →https://doi.org/10.1093/gbe/evt181openalex-snapshot
Massively Convergent Evolution for Ribosomal Protein Gene Content in Plastid and Mitochondrial Genomes
inferredcites →https://doi.org/10.1093/gbe/evt210openalex-snapshot
Genome Degeneration and Adaptation in a Nascent Stage of Symbiosis
inferredcites →https://doi.org/10.1093/gbe/evu133openalex-snapshot
Settling Down: The Genome of Serratia symbiotica from the Aphid Cinara tujafilina Zooms in on the Process of Accommodation to a Cooperative Intracellular Life
inferredcites →https://doi.org/10.1093/gbe/evv159openalex-snapshot
Lineage-Specific Patterns of Genome Deterioration in Obligate Symbionts of Sharpshooter Leafhoppers
inferredcites →https://doi.org/10.1093/gbe/evv170openalex-snapshot
Metabolic Coevolution in the Bacterial Symbiosis of Whiteflies and Related Plant Sap-Feeding Insects
inferredcites →https://doi.org/10.1093/genetics/150.1.425openalex-snapshot
A Subset of Conserved tRNA Genes in Plastid DNA of Nongreen Plants
inferredcites →https://doi.org/10.1093/jxb/erm267openalex-snapshot
Dual targeting of the tRNA nucleotidyltransferase in plants: not just the signal
inferredcites →https://doi.org/10.1093/molbev/msg167openalex-snapshot
Increased Rates of Sequence Evolution in Endosymbiotic Bacteria and Fungi with Small Effective Population Sizes
inferredcites →https://doi.org/10.1093/molbev/msr028openalex-snapshot
Rampant Gene Loss in the Underground Orchid Rhizanthella gardneri Highlights Evolutionary Constraints on Plastid Genomes
inferredcites →https://doi.org/10.1093/molbev/mss180openalex-snapshot
Genome Reduction and Co-evolution between the Primary and Secondary Bacterial Symbionts of Psyllids
inferredcites →https://doi.org/10.1093/molbev/msu004openalex-snapshot
Parallel Histories of Horizontal Gene Transfer Facilitated Extreme Reduction of Endosymbiont Genomes in Sap-Feeding Insects
inferredcites →https://doi.org/10.1093/nar/22.12.2183openalex-snapshot
Summary: the modified nucleosides of RNA
inferredcites →https://doi.org/10.1093/nar/25.5.0955openalex-snapshot
tRNAscan-SE: A Program for Improved Detection of Transfer RNA Genes in Genomic Sequence
inferredcites →https://doi.org/10.1093/nar/4.12.4165openalex-snapshot
End labeling of enzymatically decapped mRNA
inferredcites →https://doi.org/10.1093/nar/8.22.5213openalex-snapshot
A mammalian mitochondrial serine transfer RNA lacking the “dihydrouridine” loop and stem
inferredcites →https://doi.org/10.1093/nar/gkh152openalex-snapshot
ARAGORN, a program to detect tRNA genes and tmRNA genes in nucleotide sequences
inferredcites →https://doi.org/10.1093/nar/gkj084openalex-snapshot
MODOMICS: a database of RNA modification pathways
inferredcites →https://doi.org/10.1093/nar/gkm1096openalex-snapshot
Developmentally regulated cleavage of tRNAs in the bacterium Streptomyces coelicolor
inferredcites →https://doi.org/10.1093/nar/gkp093openalex-snapshot
Meta-analysis of small RNA-sequencing errors reveals ubiquitous post-transcriptional RNA modifications
inferredcites →https://doi.org/10.1093/nar/gkr450openalex-snapshot
RNA degradome--its biogenesis and functions
inferredcites →https://doi.org/10.1093/nar/gks503openalex-snapshot
Altered tRNA characteristics and 3′ maturation in bacterial symbionts with reduced genomes
inferredcites →https://doi.org/10.1093/nar/gkx103openalex-snapshot
tRNA-derived small RNAs target transposable element transcripts
inferredcites →https://doi.org/10.1101/gad.1956510openalex-snapshot
tRNA biology charges to the front
inferredcites →https://doi.org/10.1101/gr.9.9.868openalex-snapshot
CAP3: A DNA Sequence Assembly Program
inferredcites →https://doi.org/10.1111/j.1742-4658.2009.06874.xopenalex-snapshot
Protein transport in organelles: The composition, function and regulation of the Tic complex in chloroplast protein import
inferredcites →https://doi.org/10.1111/nyas.12740openalex-snapshot
Endosymbiont evolution: predictions from theory and surprises from genomes
inferredcites →https://doi.org/10.1126/science.1071278openalex-snapshot
50 Million Years of Genomic Stasis in Endosymbiotic Bacteria
inferredcites →https://doi.org/10.1126/science.1145718openalex-snapshot
Permuted tRNA Genes Expressed via a Circular RNA Intermediate in Cyanidioschyzon merolae
inferredcites →https://doi.org/10.1126/science.aaa9605openalex-snapshot
Evolving new organisms via symbiosis
inferredcites →https://doi.org/10.1128/aem.00291-10openalex-snapshot
Chromosome Stability and Gene Loss in Cockroach Endosymbionts
inferredcites →https://doi.org/10.1128/jb.00097-13openalex-snapshot
Multiple Roles of RNase Y in Streptococcus pyogenes mRNA Processing and Degradation
inferredcites →https://doi.org/10.1128/jb.05749-11openalex-snapshot
Complete Genome Sequence of “Candidatus Tremblaya princeps” Strain PCVAL, an Intriguing Translational Machine below the Living-Cell Status
inferredcites →https://doi.org/10.1128/mmbr.56.1.229-264.1992openalex-snapshot
Recent evidence for evolution of the genetic code.
inferredcites →https://doi.org/10.1146/annurev-genet-110410-132531openalex-snapshot
Human Mitochondrial tRNAs: Biogenesis, Function, Structural Aspects, and Diseases
inferredcites →https://doi.org/10.1146/annurev-micro-091213-112901openalex-snapshot
The Tiniest Tiny Genomes
inferredcites →https://doi.org/10.1146/annurev.micro.62.081307.162948openalex-snapshot
Biology of trans-Translation
inferredcites →https://doi.org/10.1186/1471-2164-10-155openalex-snapshot
Bioinformatics analysis suggests base modifications of tRNAs and miRNAs in Arabidopsis thaliana
inferredcites →https://doi.org/10.1186/1471-2164-10-598openalex-snapshot
Improved tRNA prediction in the American house dust mite reveals widespread occurrence of extremely short minimal tRNAs in acariform mites
inferredcites →https://doi.org/10.1186/1471-2164-7-297openalex-snapshot
Comparative analysis of dinoflagellate chloroplast genomes reveals rRNA and tRNA genes
inferredcites →https://doi.org/10.1186/gb-2009-10-3-r25openalex-snapshot
Ultrafast and memory-efficient alignment of short DNA sequences to the human genome
inferredcites →https://doi.org/10.1186/s12862-016-0820-zopenalex-snapshot
Development of a toolbox to dissect host-endosymbiont interactions and protein trafficking in the trypanosomatid Angomonas deanei
inferredcites →https://doi.org/10.1371/journal.pgen.1000565openalex-snapshot
Origin of an Alternative Genetic Code in the Extremely Small and GC–Rich Genome of a Bacterial Symbiont
inferredcites →https://doi.org/10.1371/journal.pgen.1000827openalex-snapshot
Bacterial Genes in the Aphid Genome: Absence of Functional Gene Transfer from Buchnera to Its Host
inferredcites →https://doi.org/10.1515/bc.2009.101openalex-snapshot
Mitochondrial tRNA import – the challenge to understand has just begun
inferredcites →https://doi.org/10.1515/bc.2011.043openalex-snapshot
Traces of post-transcriptional RNA modifications in deep sequencing data
inferredcites →https://doi.org/10.3389/fgene.2014.00109openalex-snapshot
Losing the stem-loop structure from metazoan mitochondrial tRNAs and co-evolution of interacting factors
inferredcites →https://doi.org/10.3389/fmicb.2014.00113openalex-snapshot
Trans-translation exposed: understanding the structures and functions of tmRNA-SmpB
inferredcites →https://doi.org/10.3389/fmicb.2014.00421openalex-snapshot
Ends of the line for tmRNA-SmpB
inferredcites →https://doi.org/10.4161/rna.27799openalex-snapshot
Organelle evolution, fragmented rRNAs, and Carl
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1073/pnas.1811932115openalex-snapshot
Evolution of host support for two ancient bacterial symbionts with differentially degraded genomes in a leafhopper host
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