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Mitochondrial genome of non-photosynthetic mycoheterotrophic plant Hypopitys monotropa ,its structure, gene expression and RNA editing

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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/ajb2.1286openalex-snapshot

Sequential horizontal gene transfers from different hosts in a widespread Eurasian parasitic plant, Cynomorium coccineum

inferredcites →https://doi.org/10.1002/j.1460-2075.1992.tb05149.xopenalex-snapshot

RNA editing in tobacco chloroplasts leads to the formation of a translatable psbL mRNA by a C to U substitution within the initiation codon.

inferredcites →https://doi.org/10.1002/j.1537-2197.1993.tb15299.xopenalex-snapshot

PATTERNS OF EMBRYO AND ENDOSPERM FORMATION IN MONOTROPA HYPOPITYS (MONOTROPACEAE) FROM NORTH AMERICA AND WESTERN SWEDEN

inferredcites →https://doi.org/10.1007/bf00425822openalex-snapshot

Linear mitochondrial DNAs from yeasts: telomeres with large tandem repetitions

inferredcites →https://doi.org/10.1007/s00438-002-0711-4openalex-snapshot

Structural features and expression analysis of a linear mitochondrial plasmid in rapeseed (Brassica napus L.)

inferredcites →https://doi.org/10.1007/s13199-012-0180-4openalex-snapshot

Mycorrhizal features and fungal partners of four mycoheterotrophic Monotropoideae (Ericaceae) species from Yunnan, China

inferredcites →https://doi.org/10.1016/j.biochi.2013.09.016openalex-snapshot

The plant mitochondrial genome: Dynamics and maintenance

inferredcites →https://doi.org/10.1016/j.cub.2013.10.062openalex-snapshot

Colponemids Represent Multiple Ancient Alveolate Lineages

inferredcites →https://doi.org/10.1016/j.gene.2013.11.104openalex-snapshot

The American cranberry mitochondrial genome reveals the presence of selenocysteine (tRNA-Sec and SECIS) insertion machinery in land plants

inferredcites →https://doi.org/10.1016/j.mito.2007.10.002openalex-snapshot

Linear plasmids in plant mitochondria: Peaceful coexistences or malicious invasions?

inferredcites →https://doi.org/10.1016/j.mito.2014.05.008openalex-snapshot

Comparative analysis of 11 Brassicales mitochondrial genomes and the mitochondrial transcriptome of Brassica oleracea

inferredcites →https://doi.org/10.1038/s41467-018-03423-5openalex-snapshot

The Gastrodia elata genome provides insights into plant adaptation to heterotrophy

inferredcites →https://doi.org/10.1038/srep17588openalex-snapshot

Massive gene loss in mistletoe (Viscum, Viscaceae) mitochondria

inferredcites →https://doi.org/10.1038/srep30042openalex-snapshot

Comparative analysis of plastid genomes of non-photosynthetic Ericaceae and their photosynthetic relatives

inferredcites →https://doi.org/10.1038/srep36285openalex-snapshot

Limited mitogenomic degradation in response to a parasitic lifestyle in Orobanchaceae

inferredcites →https://doi.org/10.1073/pnas.0408336102openalex-snapshot

Massive horizontal transfer of mitochondrial genes from diverse land plant donors to the basal angiosperm Amborella

inferredcites →https://doi.org/10.1073/pnas.1218884110openalex-snapshot

Characterization and comparison of human nuclear and cytosolic editomes

inferredcites →https://doi.org/10.1073/pnas.1321745111openalex-snapshot

Human coding RNA editing is generally nonadaptive

inferredcites →https://doi.org/10.1073/pnas.1504491112openalex-snapshot

Miniaturized mitogenome of the parasitic plant Viscum scurruloideum is extremely divergent and dynamic and has lost all nad genes

inferredcites →https://doi.org/10.1073/pnas.1608765113openalex-snapshot

Horizontal gene transfer is more frequent with increased heterotrophy and contributes to parasite adaptation

inferredcites →https://doi.org/10.1073/pnas.95.24.14244openalex-snapshot

Explosive invasion of plant mitochondria by a group I intron

inferredcites →https://doi.org/10.1080/23802359.2016.1155090openalex-snapshot

The complete chloroplast genome of parasitic flowering plant Monotropa hypopitys: extensive gene losses and size reduction

inferredcites →https://doi.org/10.1093/bib/bbx108openalex-snapshot

MAFFT online service: multiple sequence alignment, interactive sequence choice and visualization

inferredcites →https://doi.org/10.1093/gbe/evs006openalex-snapshot

Recent Acceleration of Plastid Sequence and Structural Evolution Coincides with Extreme Mitochondrial Divergence in the Angiosperm Genus Silene

inferredcites →https://doi.org/10.1093/gbe/evu001openalex-snapshot

The Plastid Genome of Mycoheterotrophic Monocot Petrosavia stellaris Exhibits Both Gene Losses and Multiple Rearrangements

inferredcites →https://doi.org/10.1093/gbe/evw147openalex-snapshot

Assembled Plastid and Mitochondrial Genomes, as well as Nuclear Genes, Place the Parasite Family Cynomoriaceae in the Saxifragales

inferredcites →https://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

inferredcites →https://doi.org/10.1093/molbev/msq029openalex-snapshot

Insights into the Evolution of Mitochondrial Genome Size from Complete Sequences of Citrullus lanatus and Cucurbita pepo (Cucurbitaceae)

inferredcites →https://doi.org/10.1093/molbev/msu252openalex-snapshot

Investigating the Path of Plastid Genome Degradation in an Early-Transitional Clade of Heterotrophic Orchids, and Implications for Heterotrophic Angiosperms

inferredcites →https://doi.org/10.1093/nar/17.14.5461openalex-snapshot

Chloroplast-like transfer RNA genes expressed in wheatmitochondria

inferredcites →https://doi.org/10.1093/nar/gkg795openalex-snapshot

The complete nucleotide sequence and RNA editing content of the mitochondrial genome of rapeseed (Brassica napus L.): comparative analysis of the mitochondrial genomes of rapeseed and Arabidopsis thaliana

inferredcites →https://doi.org/10.1093/nar/gkt1183openalex-snapshot

MycoCosm portal: gearing up for 1000 fungal genomes

inferredcites →https://doi.org/10.1093/nar/gkt550openalex-snapshot

SECISearch3 and Seblastian: new tools for prediction of SECIS elements and selenoproteins

inferredcites →https://doi.org/10.1101/gr.092759.109openalex-snapshot

Circos: An information aesthetic for comparative genomics

inferredcites →https://doi.org/10.1105/tpc.111.087189openalex-snapshot

Origins and Recombination of the Bacterial-Sized Multichromosomal Mitochondrial Genome of Cucumber

inferredcites →https://doi.org/10.1111/j.1399-3054.1960.tb08034.xopenalex-snapshot

Monotropa Hypopitys L. — an Epiparasite on Tree Roots

inferredcites →https://doi.org/10.1111/nph.12395openalex-snapshot

One ring to rule them all? Genome sequencing provides new insights into the ‘master circle’ model of plant mitochondrial DNA structure

inferredcites →https://doi.org/10.1111/nph.14361openalex-snapshot

Unparalleled replacement of native mitochondrial genes by foreign homologs in a holoparasitic plant

inferredcites →https://doi.org/10.1126/science.1246275openalex-snapshot

Horizontal Transfer of Entire Genomes via Mitochondrial Fusion in the Angiosperm Amborella

inferredcites →https://doi.org/10.1126/science.1253122openalex-snapshot

Genomic-scale exchange of mRNA between a parasitic plant and its hosts

inferredcites →https://doi.org/10.1186/1471-2105-10-421openalex-snapshot

BLAST+: architecture and applications

inferredcites →https://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

inferredcites →https://doi.org/10.1186/1471-2148-13-126openalex-snapshot

Parasitic plants have increased rates of molecular evolution across all three genomes

inferredcites →https://doi.org/10.1186/gb-2012-13-6-r56openalex-snapshot

Toward almost closed genomes with GapFiller

inferredcites →https://doi.org/10.1186/s12862-019-1401-8openalex-snapshot

Mitochondrial genome evolution in parasitic plants

inferredcites →https://doi.org/10.1186/s12864-018-4968-3openalex-snapshot

RNA-seq highlights parallel and contrasting patterns in the evolution of the nuclear genome of fully mycoheterotrophic plants

inferredcites →https://doi.org/10.1186/s12870-017-0992-8openalex-snapshot

Comparative mitogenomics indicates respiratory competence in parasitic Viscum despite loss of complex I and extreme sequence divergence, and reveals horizontal gene transfer and remarkable variation in genome size

inferredcites →https://doi.org/10.1371/journal.pcbi.1005383openalex-snapshot

Computational identification of the selenocysteine tRNA (tRNASec) in genomes

inferredcites →https://doi.org/10.1371/journal.pgen.1003265openalex-snapshot

Massive Mitochondrial Gene Transfer in a Parasitic Flowering Plant Clade

inferredcites →https://doi.org/10.1371/journal.pgen.1008373openalex-snapshot

The alternative reality of plant mitochondrial DNA: One ring does not rule them all

inferredcites →https://doi.org/10.1371/journal.pone.0150718openalex-snapshot

Complete Plastid Genome of the Recent Holoparasite Lathraea squamaria Reveals Earliest Stages of Plastome Reduction in Orobanchaceae

inferredcites →https://doi.org/10.1534/genetics.114.161414openalex-snapshot

Abundant and Selective RNA-Editing Events in the Medicinal Mushroom Ganoderma lucidum

What points at this work

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

inferred← citeshttps://doi.org/10.1007/s00606-023-01849-zopenalex-snapshot

Diversity of RNA editing in chloroplast transcripts across three main plant clades

inferred← citeshttps://doi.org/10.1109/kse50997.2020.9287768openalex-snapshot

Application of Next-generation Sequencing Method for Elucidating Evolutionary History of Chloroplast Genome in Plant Kingdom

inferred← citeshttps://doi.org/10.1111/jse.12655openalex-snapshot

Genomic architectural variation of plant mitochondria—A review of multichromosomal structuring

inferred← citeshttps://doi.org/10.24425/abcsb.2021.136701openalex-snapshot

Achievements in Horizontal Gene Transfer Studies in Parasitic Plants

inferred← citeshttps://doi.org/10.3390/plants9050618openalex-snapshot

Mitochondrial Genome of Fagopyrum esculentum and the Genetic Diversity of Extranuclear Genomes in Buckwheat

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