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Normal mitochondrial function in Saccharomyces cerevisiae has become dependent on inefficient splicing
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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/yea.906openalex-snapshot
Overexpressed yeast mitochondrial putative RNA helicase Mss116 partially restores proper mtRNA metabolism in strains lacking the Suv3 mtRNA helicase
inferredcites →https://doi.org/10.1007/bf00309780openalex-snapshot
The S. cerevisiae nuclear gene SUV3 encoding a putative RNA helicase is necessary for the stability of mitochondrial transcripts containing multiple introns
inferredcites →https://doi.org/10.1007/bf00326288openalex-snapshot
Distribution of mitochondrial intron sequences among 21 yeast species
inferredcites →https://doi.org/10.1016/0076-6879(83)01015-0openalex-snapshot
[12] One-step gene disruption in yeast
inferredcites →https://doi.org/10.1016/0092-8674(80)90246-9openalex-snapshot
Sequence of the intron and flanking exons of the mitochondrial 21S rRNA gene of yeast strains having different alleles at the ω and rib-1 loci
inferredcites →https://doi.org/10.1016/0092-8674(89)90245-6openalex-snapshot
A latent intron-encoded maturase is also an endonuclease needed for intron mobility
inferredcites →https://doi.org/10.1016/0378-1119(89)90034-6openalex-snapshot
Group I introns as mobile genetic elements: Facts and mechanistic speculations — a review
inferredcites →https://doi.org/10.1016/j.biocel.2009.01.011openalex-snapshot
Mitochondrial F1F0-ATP synthase and organellar internal architecture
inferredcites →https://doi.org/10.1016/j.mito.2015.07.001openalex-snapshot
MitoLoc: A method for the simultaneous quantification of mitochondrial network morphology and membrane potential in single cells
inferredcites →https://doi.org/10.1016/j.molcel.2013.06.012openalex-snapshot
Competition between Pre-mRNAs for the Splicing Machinery Drives Global Regulation of Splicing
inferredcites →https://doi.org/10.1016/s0091-679x(06)80026-9openalex-snapshot
Genetic Transformation of Saccharomyces cerevisiae and Chlamydomonas reinhardtii Mitochondria
inferredcites →https://doi.org/10.1038/35084545openalex-snapshot
The role of selfish genetic elements in eukaryotic evolution
inferredcites →https://doi.org/10.1038/nature09422openalex-snapshot
Single-molecule analysis of Mss116-mediated group II intron folding
inferredcites →https://doi.org/10.1038/nature20789openalex-snapshot
Splicing factor 1 modulates dietary restriction and TORC1 pathway longevity in C. elegans
inferredcites →https://doi.org/10.1038/nmeth.1322openalex-snapshot
Universal sample preparation method for proteome analysis
inferredcites →https://doi.org/10.1038/nprot.2007.13openalex-snapshot
High-efficiency yeast transformation using the LiAc/SS carrier DNA/PEG method
inferredcites →https://doi.org/10.1038/nrg2164openalex-snapshot
Splicing in disease: disruption of the splicing code and the decoding machinery
inferredcites →https://doi.org/10.1038/nrg2337openalex-snapshot
Transposable elements and the evolution of regulatory networks
inferredcites →https://doi.org/10.1073/pnas.0407896101openalex-snapshot
The splicing of yeast mitochondrial group I and group II introns requires a DEAD-box protein with RNA chaperone function
inferredcites →https://doi.org/10.1073/pnas.1102343108openalex-snapshot
Selfish genetic elements, genetic conflict, and evolutionary innovation
inferredcites →https://doi.org/10.1073/pnas.84.19.6810openalex-snapshot
Construction of a yeast strain devoid of mitochondrial introns and its use to screen nuclear genes involved in mitochondrial splicing.
inferredcites →https://doi.org/10.1073/pnas.96.24.13880openalex-snapshot
Recurrent invasion and extinction of a selfish gene
inferredcites →https://doi.org/10.1093/emboj/21.3.221openalex-snapshot
The ATP synthase is involved in generating mitochondrial cristae morphology
inferredcites →https://doi.org/10.1093/genetics/101.3-4.519openalex-snapshot
SELFISH DNA: A SEXUALLY-TRANSMITTED NUCLEAR PARASITE
inferredcites →https://doi.org/10.1128/mcb.00160-14openalex-snapshot
Yeast DEAD Box Protein Mss116p Is a Transcription Elongation Factor That Modulates the Activity of Mitochondrial RNA Polymerase
inferredcites →https://doi.org/10.1146/annurev.bi.62.070193.003103openalex-snapshot
INTRONS AS MOBILE GENETIC ELEMENTS
inferredcites →https://doi.org/10.1186/s12864-015-1480-xopenalex-snapshot
Identification and characterization of rye genes not expressed in allohexaploid triticale
inferredcites →https://doi.org/10.1186/s12864-015-1664-4openalex-snapshot
Population structure of mitochondrial genomes in Saccharomyces cerevisiae
inferredcites →https://doi.org/10.1371/journal.pone.0078105openalex-snapshot
The Mitochondrial RNA Landscape of Saccharomyces cerevisiae
inferredcites →https://doi.org/10.1534/genetics.116.199059openalex-snapshot
Mobile Introns Shape the Genetic Diversity of Their Host Genes
inferredcites →https://doi.org/10.2144/000113610openalex-snapshot
Mitochondrial Membrane Potential Probes and the Proton Gradient: A Practical Usage Guide
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.3897/imafungus.16.159349zenodo-depositor-declared
Characterization of the mitochondrial genomes for Ophiostoma ips and related taxa from various geographic origins and related species: large intron-rich genomes and complex intron arrangements
inferred← citeshttps://doi.org/10.1002/iub.2779openalex-snapshot
RNA processing and degradation mechanisms shaping the mitochondrial transcriptome of budding yeasts
inferred← citeshttps://doi.org/10.1002/yea.3893openalex-snapshot
Long‐read direct RNA sequencing of the mitochondrial transcriptome of Saccharomyces cerevisiae reveals condition‐dependent intron abundance
inferred← citeshttps://doi.org/10.1016/j.jbc.2022.102214openalex-snapshot
Overexpression of MRX9 impairs processing of RNAs encoding mitochondrial oxidative phosphorylation factors COB and COX1 in yeast
inferred← citeshttps://doi.org/10.1016/j.jmb.2024.168513openalex-snapshot
Highly Reactive Group I Introns Ubiquitous in Pathogenic Fungi
inferred← citeshttps://doi.org/10.1038/s41598-018-35926-yopenalex-snapshot
The mitochondrial genome of Endoconidiophora resinifera is intron rich
inferred← citeshttps://doi.org/10.1073/pnas.1806685115openalex-snapshot
Optimal molecular crowding accelerates group II intron folding and maximizes catalysis
inferred← citeshttps://doi.org/10.1093/genetics/iyad147openalex-snapshot
Mitochondrial superoxide dismutase Sod2 suppresses nuclear genome instability during oxidative stress
inferred← citeshttps://doi.org/10.1093/molbev/msaf076openalex-snapshot
An Alternative Self-Splicing Intron Lifecycle Revealed by Dynamic Intron Turnover in Epichloë Endophyte Mitochondrial Genomes
inferred← citeshttps://doi.org/10.1101/2023.01.19.524680openalex-snapshot
Long-read direct RNA sequencing of the mitochondrial transcriptome of Saccharomyces cerevisiae reveals condition-dependent intron turnover
inferred← citeshttps://doi.org/10.1139/cjm-2020-0589openalex-snapshot
The mitochondrial genome of Ophiostoma himal-ulmi and comparison with other fungi causing Dutch elm disease
inferred← citeshttps://doi.org/10.1139/cjm-2024-0179openalex-snapshot
Comparative mitogenomics of Leptographium procerum, Leptographium terebrantis, and Leptographium wingfieldii, an invasive fungal species in Canadian forests
inferred← citeshttps://doi.org/10.11606/d.42.2022.tde-02062022-155130openalex-snapshot
Identificação de proteínas do complexo MIOREX de função desconhecida que possam estar envolvidas com a tradução mitocondrial.
inferred← citeshttps://doi.org/10.1186/s12864-026-13178-9openalex-snapshot
Decoding the genome of the basidiomycetous yeast Vishniacozyma victoriae D19: a promising fungal model for biotechnology
inferred← citeshttps://doi.org/10.1590/1678-4685-gmb-2023-0228openalex-snapshot
Group I introns: Structure, splicing and their applications in medical mycology
inferred← citeshttps://doi.org/10.2174/0115734080358248250507062836openalex-snapshot
Advances in the Production of Recombinant Protease through Expression Systems: An Updated Review
inferred← citeshttps://doi.org/10.3389/fgene.2021.785218openalex-snapshot
Mutational Effects of Mobile Introns on the Mitochondrial Genomes of Metschnikowia Yeasts
inferred← citeshttps://doi.org/10.3389/fmicb.2020.628579openalex-snapshot
Editorial: The Significance of Mitogenomics in Mycology
inferred← citeshttps://doi.org/10.3389/fmicb.2021.618649openalex-snapshot
The Mitogenomes of Ophiostoma minus and Ophiostoma piliferum and Comparisons With Other Members of the Ophiostomatales
inferred← citeshttps://doi.org/10.3389/fmicb.2021.656609openalex-snapshot
Recent and Ongoing Horizontal Transfer of Mitochondrial Introns Between Two Fungal Tree Pathogens
inferred← citeshttps://doi.org/10.3389/fmicb.2022.897981openalex-snapshot
Editorial: Mitochondrial Genomes and Mitochondrion Related Gene Insights to Fungal Evolution
inferred← citeshttps://doi.org/10.3389/fmicb.2023.1240407openalex-snapshot
The mitogenomes of Leptographium aureum, Leptographium sp., and Grosmannia fruticeta: expansion by introns
inferred← citeshttps://doi.org/10.3389/fmicb.2023.1344877openalex-snapshot
Editorial: The significance of mitogenomics in mycology, volume II
inferred← citeshttps://doi.org/10.3390/antiox9020094openalex-snapshot
Cellular Aging Characteristics and Their Association with Age-Related Disorders
inferred← citeshttps://doi.org/10.3390/cells10082001openalex-snapshot
Organellar Introns in Fungi, Algae, and Plants
inferred← citeshttps://doi.org/10.3390/jof12010075openalex-snapshot
Comparative Mitogenomics Reveals Intron Dynamics and Mitochondrial Gene Expression Shifts in Domesticated and Wild Pleurotus ostreatus
inferred← citeshttps://doi.org/10.7554/elife.34268openalex-snapshot
Group II intron inhibits conjugative relaxase expression in bacteria by mRNA targeting
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