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The Mitochondrial Endonuclease M20 Participates in the Down-Regulation of Mitochondrial DNA in Pollen Cells

https://doi.org/10.1104/pp.18.00754

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What this work says

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

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Mitochondrial DNA molecules and virtual number of mitochondria per cell in mammalian cells

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Cloning and Chromosomal Mapping of the Human DNA Polymerase θ (POLQ), the Eighth Human DNA Polymerase

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Predicting Subcellular Localization of Proteins Based on their N-terminal Amino Acid Sequence

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Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method

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Organization of heterogeneous mitochondrial DNA molecules in mitochondrial nuclei of cultured tobacco cells

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Degradation of chloroplast DNA in second leaves of rice (Oryza sativa) before leaf yellowing

inferredcites →https://doi.org/10.1007/s004250050606openalex-snapshot

The selective increase or decrease of organellar DNA in generative cells just after pollen mitosis one controls cytoplasmic inheritance

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Nuclease detection in SDS-polyacrylamide gel electrophoresis

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Mouse L cell mitochondrial DNA molecules are selected randomly for replication throughout the cell cycle

inferredcites →https://doi.org/10.1016/j.bbagen.2005.03.001openalex-snapshot

Quantitative change in mitochondrial DNA content in various mouse tissues during aging

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Mimicking Cellular Sorting Improves Prediction of Subcellular Localization

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Rapid and random turnover of mitochondrial DNA in rat hepatocytes of primary culture

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Regulation of mitochondrial DNA content and cancer

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DNA degradation during programmed cell death in Phaseolus coccineus suspensor

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Replication of mitochondrial DNA occurs throughout the mitochondria of cultured human cells

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Apparent Turnover of Mitochondrial Deoxyribonucleic Acid and Mitochondrial Phospholipids in the Tissues of the Rat

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Mitochondrial diseases

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Nuclease activities associated with dark-induced and natural leaf senescence in parsley

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Number matters: control of mammalian mitochondrial DNA copy number

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Mutation of the mouse klotho gene leads to a syndrome resembling ageing.

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Efficient genome editing in plants using a CRISPR/Cas system

inferredcites →https://doi.org/10.1038/cr.2013.123openalex-snapshot

Targeted mutagenesis in rice using CRISPR-Cas system

inferredcites →https://doi.org/10.1038/ncb1345openalex-snapshot

GENERATIVE CELL SPECIFIC 1 is essential for angiosperm fertilization

inferredcites →https://doi.org/10.1038/ng.2570openalex-snapshot

A detrimental mitochondrial-nuclear interaction causes cytoplasmic male sterility in rice

inferredcites →https://doi.org/10.1046/j.1365-313x.1994.06030447.xopenalex-snapshot

Physical mapping of the mitochondrial genome of Arabidopsis thaliana by cosmid and YAC clones

inferredcites →https://doi.org/10.1046/j.1365-313x.1998.00343.xopenalex-snapshot

Floral dip: a simplified method for Agrobacterium ‐mediated transformation of Arabidopsis thaliana

inferredcites →https://doi.org/10.1073/pnas.0401077101openalex-snapshot

Frequent fusion and fission of plant mitochondria with unequal nucleoid distribution

inferredcites →https://doi.org/10.1073/pnas.0805399105openalex-snapshot

Human mitochondrial RNA polymerase primes lagging-strand DNA synthesis in vitro

inferredcites →https://doi.org/10.1073/pnas.1400822111openalex-snapshot

Multigeneration analysis reveals the inheritance, specificity, and patterns of CRISPR/Cas-induced gene modifications in Arabidopsis

inferredcites →https://doi.org/10.1073/pnas.69.7.1830openalex-snapshot

Physicochemical Characterization of Mitochondrial DNA from Pea Leaves

inferredcites →https://doi.org/10.1073/pnas.96.5.1817openalex-snapshot

Mitochondria and dystonia: The movement disorder connection?

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Mitochondrial DNA and disease

inferredcites →https://doi.org/10.1091/mbc.12.4.821openalex-snapshot

Mitochondrial Single-stranded DNA-binding Protein Is Required for Mitochondrial DNA Replication and Development inDrosophila melanogaster

inferredcites →https://doi.org/10.1093/gbe/evr123openalex-snapshot

Evolution of Linear Mitochondrial Genomes in Medusozoan Cnidarians

inferredcites →https://doi.org/10.1093/jxb/eru091openalex-snapshot

Nucleases in higher plants and their possible involvement in DNA degradation during leaf senescence

inferredcites →https://doi.org/10.1093/jxb/erx383openalex-snapshot

A novel tetratricopeptide repeat protein, WHITE TO GREEN1, is required for early chloroplast development and affects RNA editing in chloroplasts

inferredcites →https://doi.org/10.1093/nar/8.19.4321openalex-snapshot

Rapid isolation of high molecular weight plant DNA

inferredcites →https://doi.org/10.1093/nar/gkg251openalex-snapshot

Human mitochondrial DNA is packaged with TFAM

inferredcites →https://doi.org/10.1093/nar/gki783openalex-snapshot

Structural and functional characterizations of mung bean mitochondrial nucleoids

inferredcites →https://doi.org/10.1093/oxfordjournals.pcp.a077463openalex-snapshot

Studies on Plastid-Nuclei (Nucleoids) in Nicotiana tabacum L. I. Isolation of Proplastid-Nuclei from Cultured Cells and Identification of Proplastid-Nuclear Proteins

inferredcites →https://doi.org/10.1093/pcp/pcv140openalex-snapshot

Persistence and Protection of Mitochondrial DNA in the Generative Cell of Cucumber is Consistent with its Paternal Transmission

inferredcites →https://doi.org/10.1093/pcp/pcy084openalex-snapshot

Chloroplast DNA Dynamics: Copy Number, Quality Control and Degradation

inferredcites →https://doi.org/10.1101/pdb.prot4995openalex-snapshot

In Planta Visualization of Protein Interactions Using Bimolecular Fluorescence Complementation (BiFC)

inferredcites →https://doi.org/10.1104/pp.111.173849openalex-snapshot

Divergent Roles for the Two PolI-Like Organelle DNA Polymerases of Arabidopsis

inferredcites →https://doi.org/10.1104/pp.15.00437openalex-snapshot

Elevation of Pollen Mitochondrial DNA Copy Number by WHIRLY2: Altered Respiration and Pollen Tube Growth in Arabidopsis

inferredcites →https://doi.org/10.1104/pp.17.01025openalex-snapshot

Fission and Fusion of Plant Mitochondria, and Genome Maintenance

inferredcites →https://doi.org/10.1105/tpc.105.038240openalex-snapshot

Cytoplasmic Male Sterility of Rice with Boro II Cytoplasm Is Caused by a Cytotoxic Peptide and Is Restored by Two Related PPR Motif Genes via Distinct Modes of mRNA Silencing

inferredcites →https://doi.org/10.1105/tpc.109.071902openalex-snapshot

The Levels of Male Gametic Mitochondrial DNA Are Highly Regulated in Angiosperms with Regard to Mitochondrial Inheritance

inferredcites →https://doi.org/10.1105/tpc.111.084012openalex-snapshot

A Conserved, Mg2+-Dependent Exonuclease Degrades Organelle DNA duringArabidopsisPollen Development

inferredcites →https://doi.org/10.1105/tpc.16.00401openalex-snapshot

Arabidopsis JINGUBANG Is a Negative Regulator of Pollen Germination That Prevents Pollination in Moist Environments

inferredcites →https://doi.org/10.1105/tpc.7.11.1951openalex-snapshot

Identification, characterization, and purification of a tobacco endonuclease activity induced upon hypersensitive response cell death.

inferredcites →https://doi.org/10.1110/ps.03115604openalex-snapshot

HNH family subclassification leads to identification of commonality in the His‐Me endonuclease superfamily

inferredcites →https://doi.org/10.1111/j.1365-313x.2005.02561.xopenalex-snapshot

Mitochondria as a connected population: ensuring continuity of the mitochondrial genome during plant cell dedifferentiation through massive mitochondrial fusion

inferredcites →https://doi.org/10.1111/j.1365-313x.2007.03248.xopenalex-snapshot

TECHNICAL ADVANCE: Temperature as a determinant factor for increased and reproducible in vitro pollen germination in Arabidopsis thaliana

inferredcites →https://doi.org/10.1111/j.1365-313x.2010.04389.xopenalex-snapshot

Fewer genes than organelles: extremely low and variable gene copy numbers in mitochondria of somatic plant cells

inferredcites →https://doi.org/10.1111/j.1469-8137.2011.03825.xopenalex-snapshot

Characterization of an ethylene-inducible, calcium-dependent nuclease that is differentially expressed in cucumber flower development

inferredcites →https://doi.org/10.1111/j.1744-7909.2012.01134.xopenalex-snapshot

The Ca2+‐dependent DNases are Involved in Secondary Xylem Development in Eucommia ulmoides

inferredcites →https://doi.org/10.1146/annurev.cb.04.110188.001445openalex-snapshot

Biogenesis of Mitochondria

inferredcites →https://doi.org/10.1186/1471-2229-9-3openalex-snapshot

A multiple-method approach reveals a declining amount of chloroplast DNA during development in Arabidopsis

inferredcites →https://doi.org/10.1186/gb-2004-5-11-r85openalex-snapshot

Transcriptome analysis of haploid male gametophyte development in Arabidopsis

inferredcites →https://doi.org/10.1371/journal.ppat.1000589openalex-snapshot

TbPIF5 Is a Trypanosoma brucei Mitochondrial DNA Helicase Involved in Processing of Minicircle Okazaki Fragments

inferredcites →https://doi.org/10.1534/genetics.104.91769openalex-snapshot

Mitochondria as Chi

inferredcites →https://doi.org/10.3109/10520296909063335openalex-snapshot

Differential Staining of Aborted and Nonaborted Pollen

inferredcites →https://doi.org/10.4161/psb.6.9.16595openalex-snapshot

Tissue-specific organelle DNA degradation mediated by DPD1 exonuclease

inferredcites →https://doi.org/10.4238/2015.march.6.12openalex-snapshot

Quantitative changes in mitochondrial DNA copy number in various tissues of pigs during growth

What points at this work

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

inferred← citeshttps://doi.org/10.2139/ssrn.4863525openalex-extracted

The Dynamic Shift in Mitochondria from Mature Pollen Grains

inferred← citeshttps://doi.org/10.1007/s00299-025-03631-6openalex-snapshot

Biparental plastid inheritance and its implications in plastid genome engineering

inferred← citeshttps://doi.org/10.1007/s11103-024-01452-xopenalex-snapshot

Characterization of organelle DNA degradation mediated by DPD1 exonuclease in the rice genome-edited line

inferred← citeshttps://doi.org/10.1007/s12038-020-00087-6openalex-snapshot

An update and perspectives on the use of promoters in plant genetic engineering

inferred← citeshttps://doi.org/10.1016/j.cub.2024.12.037openalex-snapshot

The atypical proteome of mitochondria from mature pollen grains

inferred← citeshttps://doi.org/10.1038/s41467-025-59568-7openalex-snapshot

A nuclear-encoded endonuclease governs the paternal transmission of mitochondria in Cucumis plants

inferred← citeshttps://doi.org/10.1038/s41477-025-02216-1openalex-snapshot

ATG5–HSP90.2-mediated micromitophagy as a cytological basis for maternal inheritance of plant mitochondria

inferred← citeshttps://doi.org/10.1038/s41477-026-02242-7openalex-snapshot

High-frequency biparental inheritance of plant mitochondria upon chilling stress and loss of a genome-degrading nuclease

inferred← citeshttps://doi.org/10.1093/pcp/pcad104openalex-snapshot

Plastid Inheritance Revisited: Emerging Role of Organelle DNA Degradation in Angiosperms

inferred← citeshttps://doi.org/10.1093/plphys/kiaf168openalex-snapshot

Cytoplasmic inheritance: The transmission of plastid and mitochondrial genomes across cells and generations

inferred← citeshttps://doi.org/10.1104/pp.18.01197openalex-snapshot

Discovery of Mitochondrial Endonucleases

inferred← citeshttps://doi.org/10.3390/plants12183299openalex-snapshot

Beyond NPK: Mineral Nutrient-Mediated Modulation in Orchestrating Flowering Time

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