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Fungal origin by horizontal transfer of a plant mitochondrial group I intron in the chimeric coxI gene of Peperomia

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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.1460-2075.1984.tb02100.xopenalex-snapshot
Three variant introns of the same general class in the mitochondrial gene for cytochrome oxidase subunit 1 in Aspergillus nidulans.
inferredcites →https://doi.org/10.1002/j.1460-2075.1984.tb02102.xopenalex-snapshot
The mitochondrial genome of the fission yeast Schizosaccharomyces pombe: highly homologous introns are inserted at the same position of the otherwise less conserved cox1 genes in Schizosaccharomyces pombe and Aspergillus nidulans.
inferredcites →https://doi.org/10.1002/j.1460-2075.1992.tb05473.xopenalex-snapshot
Silent mitochondrial and active nuclear genes for subunit 2 of cytochrome c oxidase (cox2) in soybean: evidence for RNA‐mediated gene transfer.
inferredcites →https://doi.org/10.1006/jmbi.1993.1402openalex-snapshot
Analysis of the Chloroplast Large Subunit Ribosomal RNA Gene from 17 Chlamydomonas Taxa
inferredcites →https://doi.org/10.1006/jmbi.1994.1390openalex-snapshot
The Ribosomal RNA Gene Region in Acanthamoeba castellanii Mitochondrial DNA
inferredcites →https://doi.org/10.1007/978-1-4020-6754-9_12413openalex-snapshot
PAUP (phylogenetic analysis using parsimony)
inferredcites →https://doi.org/10.1007/978-1-4684-4988-4_2openalex-snapshot
The Mitochondrial Genome of Animals
inferredcites →https://doi.org/10.1007/bf00312772openalex-snapshot
Nucleotide sequence of the COX1 gene in Kluyveromyces lactis mitochondrial DNA: evidence for recent horizontal transfer of a group II intron
inferredcites →https://doi.org/10.1007/bf00334517openalex-snapshot
The complete DNA sequence of the mitochondrial genome of Podospora anserina
inferredcites →https://doi.org/10.1007/bf00340719openalex-snapshot
DNA sequence analysis of the 24.5 Kilobase pair cytochrome oxidase subunit I mitochondrial gene from Podospora anserina: a gene with sixteen introns
inferredcites →https://doi.org/10.1007/bf00355058openalex-snapshot
The mitochondrial genome of Schizosaccharomyces pombe
inferredcites →https://doi.org/10.1016/0022-2836(90)90386-zopenalex-snapshot
Modelling of the three-dimensional architecture of group I catalytic introns based on comparative sequence analysis
inferredcites →https://doi.org/10.1016/0022-2836(92)90708-ropenalex-snapshot
Gene organization deduced from the complete sequence of liverwort Marchantia polymorpha mitochondrial DNA
inferredcites →https://doi.org/10.1016/0025-5564(82)90027-xopenalex-snapshot
Branch and bound algorithms to determine minimal evolutionary trees
inferredcites →https://doi.org/10.1016/0092-8674(79)90352-0openalex-snapshot
Assembly of the mitochondrial membrane system: sequences of yeast mitochondrial valine and an unusual threonine tRNA gene
inferredcites →https://doi.org/10.1016/0092-8674(81)90011-8openalex-snapshot
RNA-mediated transfer of the gene coxII from the mitochondrion to the nucleus during flowering plant evolution
inferredcites →https://doi.org/10.1016/0092-8674(83)90331-8openalex-snapshot
The double-strand-break repair model for recombination
inferredcites →https://doi.org/10.1016/0092-8674(86)90651-3openalex-snapshot
Genetic exchanges between bacteriophage T4 and filamentous fungi?
inferredcites →https://doi.org/10.1016/0092-8674(89)90246-8openalex-snapshot
Site-specific DNA endonuclease and RNA maturase activities of two homologous intron-encoded proteins from yeast mitochondria
inferredcites →https://doi.org/10.1016/0092-8674(89)90892-1openalex-snapshot
Transfer and function of T-DNA genes from Agrobacterium Ti and Ri plasmids in plants
inferredcites →https://doi.org/10.1016/0304-4173(83)90003-4openalex-snapshot
Structure of cytochrome c oxidase
inferredcites →https://doi.org/10.1016/0378-1119(86)90027-2openalex-snapshot
The mosaic cox1 gene in the mitochondrial genome of Schizosaccharomyces pombe: minimal structural requirements and evolution of group I introns
inferredcites →https://doi.org/10.1016/0378-1119(89)90036-xopenalex-snapshot
A site-specific endonuclease and co-conversion of flanking exons associated with the mobile td intron of phage T4
inferredcites →https://doi.org/10.1016/0968-0004(92)90335-7openalex-snapshot
Evolution by acquisition: the case for horizontal gene transfers
inferredcites →https://doi.org/10.1016/1055-7903(92)90020-hopenalex-snapshot
Evolutionary relationships within the fungi: Analyses of nuclear small subunit rRNA sequences
inferredcites →https://doi.org/10.1016/b978-0-12-715007-9.50009-8openalex-snapshot
Plastid Chromosomes: Structure and Evolution
inferredcites →https://doi.org/10.1016/s0021-9258(18)43467-9openalex-snapshot
Assembly of the mitochondrial membrane system. DNA sequence and organization of the cytochrome b gene in Saccharomyces cerevisiae D273-10B.
inferredcites →https://doi.org/10.1016/s0021-9258(19)70224-5openalex-snapshot
Assembly of the mitochondrial membrane system. Structure and nucleotide sequence of the gene coding for subunit 1 of yeast cytochrme oxidase.
inferredcites →https://doi.org/10.1016/s0074-7696(08)62064-1openalex-snapshot
Evolution of Mitochondrial Genomes in Fungi
inferredcites →https://doi.org/10.1016/s0074-7696(08)62068-9openalex-snapshot
The Endosymbiont Hypothesis Revisited
inferredcites →https://doi.org/10.1016/s0723-2020(11)80277-8openalex-snapshot
Evolutionary Relationships Among Higher Fungi Inferred from Small Ribosomal Subunit RNA Sequence Analysis
inferredcites →https://doi.org/10.1038/256505a0openalex-snapshot
5S RNA secondary structure
inferredcites →https://doi.org/10.1073/pnas.74.12.5463openalex-snapshot
DNA sequencing with chain-terminating inhibitors
inferredcites →https://doi.org/10.1073/pnas.84.24.9054openalex-snapshot
Rates of nucleotide substitution vary greatly among plant mitochondrial, chloroplast, and nuclear DNAs.
inferredcites →https://doi.org/10.1073/pnas.91.2.634openalex-snapshot
Plant mitochondrial nucleic acid sequences as a tool for phylogenetic analysis.
inferredcites →https://doi.org/10.1093/bioinformatics/10.1.41openalex-snapshot
fastDNAml: a tool for construction of phylogenetic trees of DNA sequences using maximum likelihood
inferredcites →https://doi.org/10.1093/nar/15.16.6734openalex-snapshot
Nucleotide sequence of the wheat mitochondrial gene for subunit I of cytochrome oxidase
inferredcites →https://doi.org/10.1093/nar/15.18.7217openalex-snapshot
Structural conventions for group I introns
inferredcites →https://doi.org/10.1093/nar/20.21.5641openalex-snapshot
The mitochondrial gene encoding ribosomal protein S12 has been translocated to the nuclear genome inOenothera
inferredcites →https://doi.org/10.1093/nar/21.22.5242openalex-snapshot
Group I introns interrupt the chloroplastpsaB andpsbC and the mitochondrialrrnL gene inChlamydomonas
inferredcites →https://doi.org/10.1093/nar/21.3.719openalex-snapshot
Mitochondrial genes in the colourless algaPrototheca wickerhamiiresemble plant genes in their exons but fungal genes in their introns
inferredcites →https://doi.org/10.1093/nar/21.5.1297openalex-snapshot
Group I introns in the liverwort mitochondrial genome: the gene coding for subunit 1 of cytochrome oxidase shares five intron positions with its fungal counterparts
inferredcites →https://doi.org/10.1093/nar/9.22.6167openalex-snapshot
Secondary structure model for 23S ribosomal RNA
inferredcites →https://doi.org/10.1101/gad.6.7.1269openalex-snapshot
Trans and cis requirements for intron mobility in a prokaryotic system.
inferredcites →https://doi.org/10.1111/j.1558-5646.1985.tb00420.xopenalex-snapshot
CONFIDENCE LIMITS ON PHYLOGENIES: AN APPROACH USING THE BOOTSTRAP
inferredcites →https://doi.org/10.1126/science.2125747openalex-snapshot
Bacterial Origin of a Chloroplast Intron: Conserved Self-Splicing Group I Introns in Cyanobacteria
inferredcites →https://doi.org/10.1126/science.2125748openalex-snapshot
An Ancient Group I Intron Shared by Eubacteria and Chloroplasts
inferredcites →https://doi.org/10.1128/mcb.10.7.3386openalex-snapshot
Characterization of I-Ppo, an Intron-Encoded Endonuclease That Mediates Homing of a Group I Intron in the Ribosomal DNA of Physarum polycephalum
inferredcites →https://doi.org/10.1146/annurev.arplant.45.1.61openalex-snapshot
The Plant Mitochondrial Genome: Physical Structure, Information Content, RNA Editing, and Gene Migration to the Nucleus
inferredcites →https://doi.org/10.1146/annurev.bi.62.070193.003103openalex-snapshot
INTRONS AS MOBILE GENETIC ELEMENTS
inferredcites →https://doi.org/10.1146/annurev.ge.24.120190.002051openalex-snapshot
PHAGE T4 INTRONS: SELF-SPLICING AND MOBILITY
inferredcites →https://doi.org/10.1146/annurev.ge.27.120193.001315openalex-snapshot
LATERAL TRANSFER IN NATURAL POPULATIONS OF EUKARYOTES
inferredcites →https://doi.org/10.2307/2399898openalex-snapshot
Progress and Prospects in Reconstructing Plant Phylogeny

What points at this work

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

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Characterisation and comparative analysis of mitochondrial genomes of false, yellow, black and blushing morels provide insights on their structure and evolution
inferred← citeshttps://doi.org/10.1002/pei3.70087openalex-snapshot
Horizontal Gene Transfer in Plants and Implications for Biotechnology
inferred← citeshttps://doi.org/10.1002/tax.594006openalex-snapshot
Contribution of mitochondrial cox1 intron sequences to the phylogenetics of tribe Orchideae (Orchidaceae): Do the distribution and sequence of this intron in orchids also tell us something about its evolution?
inferred← citeshttps://doi.org/10.1006/mpev.1999.0680openalex-snapshot
Use of atp6 in Fungal Phylogenetics: An Example from the Boletales
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Plant phylogeography based on organelle genes: an introduction
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Extranuclear inheritance: Gene transfer out of plastids
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Mitochondrial Genome Evolution in the Plant Lineage
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Gene Expression in Higher Plant Mitochondria
inferred← citeshttps://doi.org/10.1007/978-1-4020-2400-9_6openalex-snapshot
Plant Mitochondrial Genome Evolution and Gene Transfer to the Nucleus
inferred← citeshttps://doi.org/10.1007/978-1-4614-8585-8_11openalex-snapshot
Bioinformatics Approaches to Deciphering Alien Gene Transfer: A Comprehensive Analysis
inferred← citeshttps://doi.org/10.1007/978-3-642-38146-1_15openalex-snapshot
Genomic Evolution in Orobanchaceae
inferred← citeshttps://doi.org/10.1007/978-3-7091-1130-7openalex-snapshot
Plant Genome Diversity Volume 1
inferred← citeshttps://doi.org/10.1007/978-3-7091-1130-7_9openalex-snapshot
Plant Mitochondrial Genome Diversity: The Genomics Revolution
inferred← citeshttps://doi.org/10.1007/978-81-322-2283-5_8openalex-snapshot
Organellar Genomes of Flowering Plants
inferred← citeshttps://doi.org/10.1007/978-94-007-2920-9_10openalex-snapshot
Horizontal Gene Transfer in Eukaryotes: Fungi-to-Plant and Plant-to-Plant Transfers of Organellar DNA
inferred← citeshttps://doi.org/10.1007/978-94-007-2920-9_14openalex-snapshot
Expression Profiling of Organellar Genes
inferred← citeshttps://doi.org/10.1007/978-94-007-2920-9_8openalex-snapshot
Seed Plant Mitochondrial Genomes: Complexity Evolving
inferred← citeshttps://doi.org/10.1007/pl00006324openalex-snapshot
Multiple origins of fungal group I introns located in the same position of nuclear SSU rRNA gene
inferred← citeshttps://doi.org/10.1007/pl00006349openalex-snapshot
The Peperomia Mitochondrial coxI Group I Intron: Timing of Horizontal Transfer and Subsequent Evolution of the Intron
inferred← citeshttps://doi.org/10.1007/s00122-008-0790-7openalex-snapshot
The mitochondrial genome of a cytoplasmic male sterile line of perennial ryegrass (Lolium perenne L.) contains an integrated linear plasmid-like element
inferred← citeshttps://doi.org/10.1007/s00239-004-0152-2openalex-snapshot
Divergent Histories of rDNA Group I Introns in the Lichen Family Physciaceae
inferred← citeshttps://doi.org/10.1007/s00239-005-0179-zopenalex-snapshot
Evolution of Pleopsidium (Lichenized Ascomycota) S943 Group I Introns and the Phylogeography of an Intron-Encoded Putative Homing Endonuclease
inferred← citeshttps://doi.org/10.1007/s00239-006-0279-4openalex-snapshot
Novel Group I Introns Encoding a Putative Homing Endonuclease in the Mitochondrial cox1 Gene of Scleractinian Corals
inferred← citeshttps://doi.org/10.1007/s00253-022-11880-8openalex-snapshot
Characterization of the mitogenome of Gongronella sp. w5 reveals substantial variation in Mucoromycota
inferred← citeshttps://doi.org/10.1007/s00294-002-0363-2openalex-snapshot
Identification of Ty1-copia retrotransposons in three ectomycorrhizal basidiomycetes: evolutionary relationships and use as molecular markers
inferred← citeshttps://doi.org/10.1007/s00294-004-0522-8openalex-snapshot
The mitochondrial DNA of land plants: peculiarities in phylogenetic perspective
inferred← citeshttps://doi.org/10.1007/s00294-004-0525-5openalex-snapshot
Multiple group I introns detected in the nuclear small subunit rDNA of the autosporic green alga Selenastrum capricornutum
inferred← citeshttps://doi.org/10.1007/s00294-008-0225-7openalex-snapshot
The horsetail Equisetum arvense mitochondria share two group I introns with the liverwort Marchantia, acquired a novel group II intron but lost intron-encoded ORFs
inferred← citeshttps://doi.org/10.1007/s00294-013-0418-6openalex-snapshot
Erratum to: An open reading frame for a protein involved in cytochrome c biogenesis is split into two parts in Brassica mitochondria
inferred← citeshttps://doi.org/10.1007/s002940050220openalex-snapshot
The fungal mitochondrial genome project: evolution of fungal mitochondrial genomes and their gene expression
inferred← citeshttps://doi.org/10.1007/s10142-004-0118-xopenalex-snapshot
A comparative genomic analysis of ESTs from Ustilago maydis
inferred← citeshttps://doi.org/10.1007/s10265-006-0284-0openalex-snapshot
Evolutionary origin of a plant mitochondrial group II intron from a reverse transcriptase/maturase-encoding ancestor
inferred← citeshttps://doi.org/10.1016/0167-4781(96)00041-3openalex-snapshot
Universality of mitochondrial RNA editing in cytochrome-c oxidase subunit I (coxI) among the land plants
inferred← citeshttps://doi.org/10.1016/b978-0-12-394279-1.00003-xopenalex-snapshot
The Role of Horizontal Transfer in Shaping the Plant Mitochondrial Genome
inferred← citeshttps://doi.org/10.1016/b978-0-12-394279-1.00010-7openalex-snapshot
Mitochondrial Genome Evolution and the Emergence of PPR Proteins
inferred← citeshttps://doi.org/10.1016/j.fgb.2005.07.001openalex-snapshot
The mitochondrial apocytochrome b genes of two Agrocybe species suggest lateral transfers of group I homing introns among phylogenetically distant fungi
inferred← citeshttps://doi.org/10.1016/j.fgb.2013.01.009openalex-snapshot
The 135 kbp mitochondrial genome of Agaricus bisporus is the largest known eukaryotic reservoir of group I introns and plasmid-related sequences
inferred← citeshttps://doi.org/10.1016/j.funeco.2013.05.003openalex-snapshot
DNA barcodes for marine fungal identification and discovery
inferred← citeshttps://doi.org/10.1016/j.mito.2020.03.008openalex-snapshot
Mitochondria in parasitic plants
inferred← citeshttps://doi.org/10.1016/j.mito.2020.06.002openalex-snapshot
Variation in protein gene and intron content among land plant mitogenomes
inferred← citeshttps://doi.org/10.1016/j.plantsci.2004.03.018openalex-snapshot
Barnase gene inserted in the intron of GUS?a model for controlling transgene flow in host plants
inferred← citeshttps://doi.org/10.1016/j.tplants.2009.10.001openalex-snapshot
The give-and-take of DNA: horizontal gene transfer in plants
inferred← citeshttps://doi.org/10.1016/j.ympev.2010.02.013openalex-snapshot
Evolutionary dynamics of introns and homing endonuclease ORFs in a region of the large subunit of the mitochondrial rRNA in Glomus species (arbuscular mycorrhizal fungi, Glomeromycota)
inferred← citeshttps://doi.org/10.1016/s0378-1119(98)00235-2openalex-snapshot
Distinctive origins of group I introns found in the COXI genes of three green algae
inferred← citeshttps://doi.org/10.1016/s0378-1119(98)00421-1openalex-snapshot
Molecular analysis of the split cox1 gene from the Basidiomycota Agrocybe aegerita: relationship of its introns with homologous Ascomycota introns and divergence levels from common ancestral copies
inferred← citeshttps://doi.org/10.1016/s0764-4469(00)01293-2openalex-snapshot
From gene to protein in higher plant mitochondria
inferred← citeshttps://doi.org/10.1016/s0953-7562(96)80211-5openalex-snapshot
One stop mycology
inferred← citeshttps://doi.org/10.1016/s1055-7903(02)00030-1openalex-snapshot
Evolution of rbcL group IA introns and intron open reading frames within the colonial Volvocales (Chlorophyceae)
inferred← citeshttps://doi.org/10.1016/s1067-5701(98)80006-5openalex-snapshot
Mitochondrial genomes
inferred← citeshttps://doi.org/10.1016/s1387-2656(08)70031-0openalex-snapshot
Group I introns in biotechnology: prospects of application of ribozymes and rare-cutting homing endonucleases
inferred← citeshttps://doi.org/10.1016/s1434-4610(98)70015-xopenalex-snapshot
The Origin and Evolution of Protist Group I Introns
inferred← citeshttps://doi.org/10.1016/s1874-5334(02)80015-6openalex-snapshot
Arbuscular mycorrhizal fungi as biostimulants and bioprotectants of crops
inferred← citeshttps://doi.org/10.1038/s41597-019-0201-8openalex-snapshot
Deciphering tea tree chloroplast and mitochondrial genomes of Camellia sinensis var. assamica
inferred← citeshttps://doi.org/10.1038/s41598-017-07886-2openalex-snapshot
Horizontal transfer of a ß-1,6-glucanase gene from an ancestral species of fungal endophyte to a cool-season grass host
inferred← citeshttps://doi.org/10.1038/s41598-018-30297-wopenalex-snapshot
Complete sequence of kenaf (Hibiscus cannabinus) mitochondrial genome and comparative analysis with the mitochondrial genomes of other plants
inferred← citeshttps://doi.org/10.1038/s41598-023-49822-7openalex-snapshot
First complete mitogenome of Massarineae and its contribution to phylogenetic implications in Pleosporales
inferred← citeshttps://doi.org/10.1038/srep36285openalex-snapshot
Limited mitogenomic degradation in response to a parasitic lifestyle in Orobanchaceae
inferred← citeshttps://doi.org/10.1073/pnas.95.24.14003openalex-snapshot
Mass migration of a group I intron: Promiscuity on a grand scale
inferred← citeshttps://doi.org/10.1073/pnas.95.24.14244openalex-snapshot
Explosive invasion of plant mitochondria by a group I intron
inferred← citeshttps://doi.org/10.1073/pnas.96.24.13880openalex-snapshot
Recurrent invasion and extinction of a selfish gene
inferred← citeshttps://doi.org/10.1073/pnas.97.13.6960openalex-snapshot
Dynamic evolution of plant mitochondrial genomes: Mobile genes and introns and highly variable mutation rates
inferred← citeshttps://doi.org/10.1080/00275514.1997.12026784openalex-snapshot
RNA accumulation and genes expressed in spores of the arbuscular mycorrhizal fungus,Gigaspora rosea
inferred← citeshttps://doi.org/10.1080/24701394.2025.2482202openalex-snapshot
Description and characterization of the small mitochondrial genome of Trichoderma cerinum (Hypocreales, Hypocreaceae) and its evolutionary perspectives
inferred← citeshttps://doi.org/10.1093/gbe/evaa126openalex-snapshot
The Coevolution of Fungal Mitochondrial Introns and Their Homing Endonucleases (GIY-YIG and LAGLIDADG)
inferred← citeshttps://doi.org/10.1093/gbe/evu028openalex-snapshot
High Variability of Mitochondrial Gene Order among Fungi
inferred← citeshttps://doi.org/10.1093/gbe/evw233openalex-snapshot
Loss of aTrans-Splicingnad1Intron from Geraniaceae and Transfer of the Maturase GenematRto the Nucleus inPelargonium
inferred← citeshttps://doi.org/10.1093/molbev/msm241openalex-snapshot
Reevaluation of the cox1 Group I Intron in Araceae and Angiosperms Indicates a History Dominated by Loss rather than Horizontal Transfer
inferred← citeshttps://doi.org/10.1093/molbev/msn129openalex-snapshot
Frequent, Phylogenetically Local Horizontal Transfer of the cox1 Group I Intron in Flowering Plant Mitochondria
inferred← citeshttps://doi.org/10.1093/molbev/mss088openalex-snapshot
Group I Intron–Mediated Trans-splicing in Mitochondria of Gigaspora rosea and a Robust Phylogenetic Affiliation of Arbuscular Mycorrhizal Fungi with Mortierellales
inferred← citeshttps://doi.org/10.1093/molbev/msu343openalex-snapshot
Comparative Transcriptome Analyses Reveal Core Parasitism Genes and Suggest Gene Duplication and Repurposing as Sources of Structural Novelty
inferred← citeshttps://doi.org/10.1093/molbev/msz198openalex-snapshot
Ancient Mitochondrial Gene Transfer between Fungi and the Orchids
inferred← citeshttps://doi.org/10.1093/nar/27.11.2339openalex-snapshot
Group II intron splicing in Escherichia coli: phenotypes of cis-acting mutations resemble splicing defects observed in organelle RNA processing
inferred← citeshttps://doi.org/10.1093/nar/gki199openalex-snapshot
Comparative mitochondrial genomics in zygomycetes: bacteria-like RNase P RNAs, mobile elements and a close source of the group I intron invasion in angiosperms
inferred← citeshttps://doi.org/10.1093/nar/gkp532openalex-snapshot
A trans -splicing group I intron and tRNA-hyperediting in the mitochondrial genome of the lycophyte Isoetes engelmannii
inferred← citeshttps://doi.org/10.1093/nar/gkr105openalex-snapshot
Elimination of a group II intron from a plastid gene causes a mutant phenotype
inferred← citeshttps://doi.org/10.1093/nar/gkz1194openalex-snapshot
A functional twintron, ‘zombie’ twintrons and a hypermobile group II intron invading itself in plant mitochondria
inferred← citeshttps://doi.org/10.1093/nar/gkz370openalex-snapshot
Rapid functional activation of a horizontally transferred eukaryotic gene in a bacterial genome in the absence of selection
inferred← citeshttps://doi.org/10.1093/oxfordjournals.molbev.a026206openalex-snapshot
Multiple acquisitions via horizontal transfer of a group I intron in the mitochondrial cox1 gene during evolution of the Araceae family
inferred← citeshttps://doi.org/10.1098/rspb.2001.1830openalex-snapshot
Outcrossed sex allows a selfish gene to invade yeast populations
inferred← citeshttps://doi.org/10.1101/532853openalex-snapshot
Deciphering tea tree chloroplast and mitochondrial genomes of Camellia sinensis var. assamica
inferred← citeshttps://doi.org/10.1104/pp.107.095653openalex-snapshot
Magnaporthe griseaInfection Triggers RNA Variation and Antisense Transcript Expression in Rice
inferred← citeshttps://doi.org/10.1105/tpc.11.9.1675openalex-snapshot
Complete Sequence of the Mitochondrial DNA of the Red Alga Porphyra purpurea: Cyanobacterial Introns and Shared Ancestry of Red and Green Algae
inferred← citeshttps://doi.org/10.1105/tpc.16.00398openalex-snapshot
The Reverse Transcriptase/RNA Maturase Protein MatR Is Required for the Splicing of Various Group II Introns in Brassicaceae Mitochondria
inferred← citeshttps://doi.org/10.1111/1462-2920.14783openalex-snapshot
Mitochondrial‐encoded endonucleases drive recombination of protein‐coding genes in yeast
inferred← citeshttps://doi.org/10.1111/bij.12872openalex-snapshot
Speciation through the looking-glass
inferred← citeshttps://doi.org/10.1111/j.1469-8137.2009.02834.xopenalex-snapshot
The mitochondrial genome sequence of the arbuscular mycorrhizal fungus Glomus intraradices isolate 494 and implications for the phylogenetic placement of Glomus
inferred← citeshttps://doi.org/10.1111/j.1469-8137.2009.02885.xopenalex-snapshot
The complete Glomus intraradices mitochondrial genome sequence – a milestone in mycorrhizal research
inferred← citeshttps://doi.org/10.1111/j.1469-8137.2010.03262.xopenalex-snapshot
DNA barcoding of arbuscular mycorrhizal fungi
inferred← citeshttps://doi.org/10.1111/j.1755-0998.2009.02637.xopenalex-snapshot
Evaluation of mitochondrial genes as DNA barcode for Basidiomycota
inferred← citeshttps://doi.org/10.1111/jpy.12126openalex-snapshot
Phylogenetic analysis of LSU and SSU r DNA group I introns of lichen photobionts associated with the genera X anthoria and X anthomendoza ( T eloschistaceae, lichenized A scomycetes)
inferred← citeshttps://doi.org/10.1111/nph.14135openalex-snapshot
Complete mitochondrial genomes from the ferns Ophioglossum californicum and Psilotum nudum are highly repetitive with the largest organellar introns
inferred← citeshttps://doi.org/10.1146/annurev.phyto.38.1.325openalex-snapshot
Role of Horizontal Gene Transfer in the Evolution of Fungi
inferred← citeshttps://doi.org/10.1186/1471-2148-11-239openalex-snapshot
Computational archaeology of the Pristionchus pacificus genome reveals evidence of horizontal gene transfers from insects
inferred← citeshttps://doi.org/10.1186/1471-2148-11-277openalex-snapshot
Multiple recent horizontal transfers of the cox1intron in Solanaceae and extended co-conversion of flanking exons
inferred← citeshttps://doi.org/10.1186/1471-2148-4-40openalex-snapshot
Phylogenetic inference in Rafflesiales: the influence of rate heterogeneity and horizontal gene transfer
inferred← citeshttps://doi.org/10.1186/1741-7007-8-150openalex-snapshot
Horizontal acquisition of multiple mitochondrial genes from a parasitic plant followed by gene conversion with host mitochondrial genes
inferred← citeshttps://doi.org/10.1186/s12862-015-0556-1openalex-snapshot
Mitochondrial group I and group II introns in the sponge orders Agelasida and Axinellida
inferred← citeshttps://doi.org/10.1186/s12862-017-0928-9openalex-snapshot
Evolution of group I introns in Porifera: new evidence for intron mobility and implications for DNA barcoding
inferred← citeshttps://doi.org/10.1186/s12862-023-02108-yopenalex-snapshot
Categorizing 161 plant (streptophyte) mitochondrial group II introns into 29 families of related paralogues finds only limited links between intron mobility and intron-borne maturases
inferred← citeshttps://doi.org/10.1186/s12864-019-5732-zopenalex-snapshot
Mobile genetic elements explain size variation in the mitochondrial genomes of four closely-related Armillaria species
inferred← citeshttps://doi.org/10.1186/s12870-019-1932-6openalex-snapshot
Comprehensive analyses of ZFP gene family and characterization of expression profiles during plant hormone response in cotton
inferred← citeshttps://doi.org/10.1201/b19543-7openalex-snapshot
Molecular biology of mitochondria: Genome, transcriptome, and proteome
inferred← citeshttps://doi.org/10.1261/rna.056572.116openalex-snapshot
Monilophyte mitochondrial rps1 genes carry a unique group II intron that likely originated from an ancient paralog in rpl2
inferred← citeshttps://doi.org/10.1271/bbb.64.606openalex-snapshot
Group I Intron Located in PR Protein Homologue Gene inYoungia japonica
inferred← citeshttps://doi.org/10.1371/journal.pone.0014048openalex-snapshot
The Agaricus bisporus cox1 Gene: The Longest Mitochondrial Gene and the Largest Reservoir of Mitochondrial Group I Introns
inferred← citeshttps://doi.org/10.1371/journal.pone.0037307openalex-snapshot
Separate Origins of Group I Introns in Two Mitochondrial Genes of the Katablepharid Leucocryptos marina
inferred← citeshttps://doi.org/10.1371/journal.pone.0049096openalex-snapshot
Frequent Gain and Loss of Introns in Fungal Cytochrome b Genes
inferred← citeshttps://doi.org/10.1371/journal.pone.0069476openalex-snapshot
The Complete Mitochondrial Genome of Gossypium hirsutum and Evolutionary Analysis of Higher Plant Mitochondrial Genomes
inferred← citeshttps://doi.org/10.1371/journal.pone.0163990openalex-snapshot
Complete Sequence and Analysis of Coconut Palm (Cocos nucifera) Mitochondrial Genome
inferred← citeshttps://doi.org/10.1371/journal.pone.0180484openalex-snapshot
The mitochondrial genome of the terrestrial carnivorous plant Utricularia reniformis (Lentibulariaceae): Structure, comparative analysis and evolutionary landmarks
inferred← citeshttps://doi.org/10.1371/journal.pone.0185545openalex-snapshot
The mitochondrial genome of the plant-pathogenic fungus Stemphylium lycopersici uncovers a dynamic structure due to repetitive and mobile elements
inferred← citeshttps://doi.org/10.1371/journal.pone.0248054openalex-snapshot
Revealing the high variability on nonconserved core and mobile elements of Austropuccinia psidii and other rust mitochondrial genomes
inferred← citeshttps://doi.org/10.1534/g3.113.009910openalex-snapshot
Horizontal Transfer and Gene Conversion as an Important Driving Force in Shaping the Landscape of Mitochondrial Introns
inferred← citeshttps://doi.org/10.18297/etd/3748openalex-snapshot
Investigation of mitochondrial inheritance in the smut fungus sporisorium reilianum.
inferred← citeshttps://doi.org/10.24425/abcsb.2021.136701openalex-snapshot
Achievements in Horizontal Gene Transfer Studies in Parasitic Plants
inferred← citeshttps://doi.org/10.3389/fmicb.2023.1141087openalex-snapshot
Trichoderma koningiopsis (Hypocreaceae) has the smallest mitogenome of the genus Trichoderma
inferred← citeshttps://doi.org/10.3389/fphys.2024.1264359openalex-snapshot
Comparative mitogenomic analysis of Sporisorium reilianum f. sp. zeae suggests recombination events during its evolutionary history
inferred← citeshttps://doi.org/10.3389/fpls.2021.802321openalex-snapshot
The Complete Mitogenome of Elymus sibiricus and Insights Into Its Evolutionary Pattern Based on Simple Repeat Sequences of Seed Plant Mitogenomes
inferred← citeshttps://doi.org/10.3390/cells10082001openalex-snapshot
Organellar Introns in Fungi, Algae, and Plants
inferred← citeshttps://doi.org/10.3390/ijms24032566openalex-snapshot
A MYB Transcription Factor Atlas Provides Insights into the Evolution of Environmental Adaptations in Plants
inferred← citeshttps://doi.org/10.3390/life11080857openalex-snapshot
Horizontal Gene Transfers in Plants
inferred← citeshttps://doi.org/10.35537/10915/73593openalex-snapshot
Mancha gris de la hoja del tomate: identificación, biología y genómica del agente etiológico
inferred← citeshttps://doi.org/10.3732/ajb.1000370openalex-snapshot
What can we learn from tobacco and other Solanaceae about horizontal DNA transfer?
inferred← citeshttps://doi.org/10.5282/edoc.14076openalex-snapshot
Molecular phylogeny, taxonomy and evolution of arbuscular mycorrhizal fungi
inferred← citeshttps://doi.org/10.53846/goediss-3490openalex-snapshot
Molecular evidence for the antiquity of group I introns inter-rupting transfer RNA genes in cyanobacteria
inferred← citeshttps://doi.org/10.5586/asbp.2014.041openalex-snapshot
Involvement of plastid, mitochondrial and nuclear genomes in plant-to-plant horizontal gene transfer
inferred← citeshttps://doi.org/10.5642/aliso.20062201.51openalex-snapshot
Phlogeny and Biogeography of the Prayer Plant Family
inferred← citeshttps://doi.org/10.6090/jarq.48.17openalex-snapshot
Post-transcriptional Regulation in Mitochondria of Rice and Wheat at Low Temperatures
inferred← citeshttps://doi.org/10.70675/2e7be73bz95e1z44efza427z0a59d645b763openalex-snapshot
Étude des transferts horizontaux dans la réserve naturelle nationale de la forêt de la Massane par une approche de génomique des écosystèmes
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