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Chloroplast competition is controlled by lipid biosynthesis in evening primroses

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

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Why are most organelle genomes transmitted maternally?
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RAPID SCREENING METHOD TO DETECT POTENTIAL BIPARENTAL INHERITANCE OF PLASTID DNA AND RESULTS FOR OVER 200 ANGIOSPERM SPECIES
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Regulation of Spinach Chloroplast Acetyl-CoA Carboxylase
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Role of Lipids in Chloroplast Biogenesis
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Plastome Mutants of Higher Plants
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Plastid Genomes of Seed Plants
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The Oenothera plastome mutator : effect of UV irradiation and nitroso-methyl urea on mutation frequencies
inferredcites →https://doi.org/10.1007/bf00280368openalex-snapshot
Oenothera chloroplast DNA polymorphisms associated with plastome mutator activity
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Electron microscopic localization of replication origins in Oenothera chloroplast DNA
inferredcites →https://doi.org/10.1007/bf00351493openalex-snapshot
Similarity between putative ATP-binding sites in land plant plastid ORF2280 proteins and the FtsH/CDC48 family of ATPases
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Plastid inheritance in Oenothera: organelle genome modifies the extent of biparental plastid transmission
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The rôle of the plastome in evolution of the genusOenothera
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Über Plastidenkonkurrenz bei Oenothera
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Oenothera—An ideal system for studying the interactions of genome and plastome
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Genetical experiments withSilene Otites and related species
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Genetic analysis of nuclear-cytoplasmic incompatibility in pea associated with cytoplasm of an accession of wild subspecies Pisum sativum subsp. elatius (Bieb.) Schmahl.
inferredcites →https://doi.org/10.1007/s002940050165openalex-snapshot
Characterization of primary lesions caused by the plastome mutator of Oenothera
inferredcites →https://doi.org/10.1007/s00438-007-0222-4openalex-snapshot
High diversity of plastidial promoters in Arabidopsis thaliana
inferredcites →https://doi.org/10.1007/s10265-009-0291-zopenalex-snapshot
Why does biparental plastid inheritance revive in angiosperms?
inferredcites →https://doi.org/10.1007/s10577-013-9349-9openalex-snapshot
DNA abandonment and the mechanisms of uniparental inheritance of mitochondria and chloroplasts
inferredcites →https://doi.org/10.1007/s11103-011-9762-4openalex-snapshot
The evolution of the plastid chromosome in land plants: gene content, gene order, gene function
inferredcites →https://doi.org/10.1016/0022-5193(81)90181-8openalex-snapshot
Cytoplasmic inheritance and intragenomic conflict
inferredcites →https://doi.org/10.1016/j.bbalip.2016.04.004openalex-snapshot
Regulation and structure of the heteromeric acetyl-CoA carboxylase
inferredcites →https://doi.org/10.1016/j.bbamcr.2011.08.015openalex-snapshot
Structure and function of the bacterial AAA protease FtsH
inferredcites →https://doi.org/10.1016/j.molp.2016.04.014openalex-snapshot
Once upon a Time – Chloroplast Protein Import Research from Infancy to Future Challenges
inferredcites →https://doi.org/10.1016/j.molp.2016.10.012openalex-snapshot
Ycf1/Tic214 Is Not Essential for the Accumulation of Plastid Proteins
inferredcites →https://doi.org/10.1016/j.plipres.2016.11.001openalex-snapshot
Importance of phosphatidylcholine on the chloroplast surface
inferredcites →https://doi.org/10.1016/j.tree.2004.10.003openalex-snapshot
Cytonuclear coevolution: the genomics of cooperation
inferredcites →https://doi.org/10.1016/s0003-9861(02)00025-5openalex-snapshot
The multisubunit acetyl-CoA carboxylase is strongly associated with the chloroplast envelope through non-ionic interactions to the carboxyltransferase subunits
inferredcites →https://doi.org/10.1017/cbo9780511975943.005openalex-snapshot
Nucleo-cytoplasmic conflict and the evolution of gamete dimorphism
inferredcites →https://doi.org/10.1038/hdy.1994.19openalex-snapshot
Organelle inheritance in plants
inferredcites →https://doi.org/10.1038/hdy.1997.207openalex-snapshot
Nonrandom partition of mitochondria in heteroplasmic Drosophila
inferredcites →https://doi.org/10.1038/ng.3587openalex-snapshot
Selfish drive can trump function when animal mitochondrial genomes compete
inferredcites →https://doi.org/10.1073/pnas.0709121104openalex-snapshot
Analysis of 81 genes from 64 plastid genomes resolves relationships in angiosperms and identifies genome-scale evolutionary patterns
inferredcites →https://doi.org/10.1073/pnas.92.25.11331openalex-snapshot
Uniparental inheritance of mitochondrial and chloroplast genes: mechanisms and evolution.
inferredcites →https://doi.org/10.1074/jbc.m103525200openalex-snapshot
Thiol-Disulfide Exchange between Nuclear-encoded and Chloroplast-encoded Subunits of Pea Acetyl-CoA Carboxylase
inferredcites →https://doi.org/10.1086/411855openalex-snapshot
Evolutionary Consequences of Intracellular Organelle Competition
inferredcites →https://doi.org/10.1093/bioinformatics/btq033openalex-snapshot
BEDTools: a flexible suite of utilities for comparing genomic features
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Geneious Basic: An integrated and extendable desktop software platform for the organization and analysis of sequence data
inferredcites →https://doi.org/10.1093/emboj/16.13.4041openalex-snapshot
The two RNA polymerases encoded by the nuclear and the plastid compartments transcribe distinct groups of genes in tobacco plastids
inferredcites →https://doi.org/10.1093/genetics/149.1.347openalex-snapshot
Plastome Mutator–Induced Alterations Arise in Oenothera Chloroplast DNA Through Template Slippage
inferredcites →https://doi.org/10.1093/genetics/75.3.465openalex-snapshot
NUCLEAR GENE-INDUCED PLASTOME MUTATIONS IN OENOTHERA HOOKERI. I. GENETIC ANALYSIS
inferredcites →https://doi.org/10.1093/nar/22.22.4673openalex-snapshot
CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice
inferredcites →https://doi.org/10.1093/nar/gkn081openalex-snapshot
The complete nucleotide sequences of the five genetically distinct plastid genomes of Oenothera , subsection Oenothera : I. Sequence evaluation and plastome evolution †
inferredcites →https://doi.org/10.1093/nar/gkt289openalex-snapshot
OrganellarGenomeDRAW—a suite of tools for generating physical maps of plastid and mitochondrial genomes and visualizing expression data sets
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a025645openalex-snapshot
Proliferation of direct repeats near the Oenothera chloroplast DNA origin of replication
inferredcites →https://doi.org/10.1093/pcp/pch021openalex-snapshot
Possible Involvement of the 5′-Flanking Region and the 5′UTR of Plastid accD Gene in NEP-Dependent Transcription
inferredcites →https://doi.org/10.1093/pcp/pcn069openalex-snapshot
Occurrence of Plastids in the Sperm Cells of Caprifoliaceae: Biparental Plastid Inheritance in Angiosperms is Unilaterally Derived from Maternal Inheritance
inferredcites →https://doi.org/10.1101/gr.209402openalex-snapshot
Comparative Analysis of Chloroplast Genomes: Functional Annotation, Genome-Based Phylogeny, and Deduced Evolutionary Patterns
inferredcites →https://doi.org/10.1105/tpc.114.135541openalex-snapshot
YCF1: A Green TIC?
inferredcites →https://doi.org/10.1105/tpc.15.00879openalex-snapshot
Spontaneous Chloroplast Mutants Mostly Occur by Replication Slippage and Show a Biased Pattern in the Plastome of Oenothera
inferredcites →https://doi.org/10.1111/j.1365-294x.2010.04984.xopenalex-snapshot
The role of plastids in plant speciation
inferredcites →https://doi.org/10.1111/j.1469-8137.2005.01492.xopenalex-snapshot
Inheritance and recombination of mitochondrial genomes in plants, fungi and animals
inferredcites →https://doi.org/10.1111/j.2517-6161.1996.tb02080.xopenalex-snapshot
Regression Shrinkage and Selection Via the Lasso
inferredcites →https://doi.org/10.1111/nph.14222openalex-snapshot
Biparental chloroplast inheritance leads to rescue from cytonuclear incompatibility
inferredcites →https://doi.org/10.1126/science.1229262openalex-snapshot
Uncovering the Protein Translocon at the Chloroplast Inner Envelope Membrane
inferredcites →https://doi.org/10.1146/annurev-arplant-050213-035748openalex-snapshot
Division and Dynamic Morphology of Plastids
inferredcites →https://doi.org/10.1146/annurev.genet.35.102401.090231openalex-snapshot
The Inheritance of Genes in Mitochondria and Chloroplasts: Laws, Mechanisms, and Models
inferredcites →https://doi.org/10.1186/s12862-014-0268-yopenalex-snapshot
Correlation between sequence divergence and polymorphism reveals similar evolutionary mechanisms acting across multiple timescales in a rapidly evolving plastid genome
inferredcites →https://doi.org/10.1371/journal.pone.0119835openalex-snapshot
Nuclear-Cytoplasmic Conflict in Pea (Pisum sativum L.) Is Associated with Nuclear and Plastidic Candidate Genes Encoding Acetyl-CoA Carboxylase Subunits
inferredcites →https://doi.org/10.1534/genetics.110.118265openalex-snapshot
Differential Replication of Two Chloroplast Genome Forms in Heteroplasmic Chlamydomonas reinhardtii Gametes Contributes to Alternative Inheritance Patterns
inferredcites →https://doi.org/10.1534/genetics.116.188268openalex-snapshot
Positive Selection in Rapidly Evolving Plastid–Nuclear Enzyme Complexes
inferredcites →https://doi.org/10.2307/25027870openalex-snapshot
Systematics of Oenothera Section Oenothera Subsection Oenothera (Onagraceae)
inferredcites →https://doi.org/10.3389/fpls.2014.00038openalex-snapshot
Growing evening primroses (Oenothera)
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