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Mitochondrial CLPP2 Assists Coordination and Homeostasis of Respiratory Complexes

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

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Histochemical staining and quantification of dihydrolipoamide dehydrogenase diaphorase activity using blue native PAGE
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The general mitochondrial processing peptidase from potato is an integral part of cytochrome c reductase of the respiratory chain.
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An improved workflow for quantitative N‐terminal charge‐based fractional diagonal chromatography (ChaFRADIC) to study proteolytic events in Arabidopsis thaliana
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A Rapid and Sensitive Method for the Quantitation of Microgram Quantities of Protein Utilizing the Principle of Protein-Dye Binding
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Activity Assay for Plant Mitochondrial Enzymes
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In Vitro and In Vivo Protein Uptake Studies in Plant Mitochondria
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Activity Measurements of Mitochondrial Enzymes in Native Gels
inferredcites →https://doi.org/10.1007/978-1-61779-234-2_8openalex-snapshot
Studying Arabidopsis Chloroplast Structural Organisation Using Transmission Electron Microscopy
inferredcites →https://doi.org/10.1007/s00425-006-0292-2openalex-snapshot
A nuclear-encoded ClpP subunit of the chloroplast ATP-dependent Clp protease is essential for early development in Arabidopsis thaliana
inferredcites →https://doi.org/10.1016/0076-6879(94)44027-1openalex-snapshot
[25] ATP-dependent protease La (Lon) from Escherichia coli
inferredcites →https://doi.org/10.1016/j.bbabio.2010.12.003openalex-snapshot
The Clp protease system; a central component of the chloroplast protease network
inferredcites →https://doi.org/10.1016/j.bbabio.2018.09.162openalex-snapshot
Protein turnover within mitochondrial complexes
inferredcites →https://doi.org/10.1016/j.bbagrm.2011.11.008openalex-snapshot
Matrix proteases in mitochondrial DNA function
inferredcites →https://doi.org/10.1016/j.biochi.2013.12.012openalex-snapshot
Phenotypical consequences of expressing the dually targeted Presequence Protease, AtPreP, exclusively in mitochondria
inferredcites →https://doi.org/10.1016/j.ccell.2015.05.004openalex-snapshot
Inhibition of the Mitochondrial Protease ClpP as a Therapeutic Strategy for Human Acute Myeloid Leukemia
inferredcites →https://doi.org/10.1016/j.febslet.2007.04.076openalex-snapshot
ClpP: A distinctive family of cylindrical energy‐dependent serine proteases
inferredcites →https://doi.org/10.1016/j.freeradbiomed.2015.12.021openalex-snapshot
Down-regulation of the mitochondrial matrix peptidase ClpP in muscle cells causes mitochondrial dysfunction and decreases cell proliferation
inferredcites →https://doi.org/10.1016/j.tig.2008.08.007openalex-snapshot
MMEJ repair of double-strand breaks (director’s cut): deleted sequences and alternative endings
inferredcites →https://doi.org/10.1016/s1097-2765(03)00060-1openalex-snapshot
Proteomic Discovery of Cellular Substrates of the ClpXP Protease Reveals Five Classes of ClpX-Recognition Signals
inferredcites →https://doi.org/10.1021/acschembio.8b00124openalex-snapshot
The Role of ClpP Protease in Bacterial Pathogenesis and Human Diseases
inferredcites →https://doi.org/10.1021/pr300394ropenalex-snapshot
Trapping and Proteomic Identification of Cellular Substrates of the ClpP Protease in Staphylococcus aureus
inferredcites →https://doi.org/10.1021/pr400435dopenalex-snapshot
Novel Highly Sensitive, Specific, and Straightforward Strategy for Comprehensive N-Terminal Proteomics Reveals Unknown Substrates of the Mitochondrial Peptidase Icp55
inferredcites →https://doi.org/10.1038/nature18015openalex-snapshot
Synchronized mitochondrial and cytosolic translation programs
inferredcites →https://doi.org/10.1038/nbt.1511openalex-snapshot
MaxQuant enables high peptide identification rates, individualized p.p.b.-range mass accuracies and proteome-wide protein quantification
inferredcites →https://doi.org/10.1038/ncomms2397openalex-snapshot
Human CLPP reverts the longevity phenotype of a fungal ClpP deletion strain
inferredcites →https://doi.org/10.1038/nmeth.2812openalex-snapshot
E-CRISP: fast CRISPR target site identification
inferredcites →https://doi.org/10.1038/nmeth.4197openalex-snapshot
Salmon provides fast and bias-aware quantification of transcript expression
inferredcites →https://doi.org/10.1038/nprot.2017.147openalex-snapshot
Proteome-wide identification of ubiquitin interactions using UbIA-MS
inferredcites →https://doi.org/10.1038/s41467-020-15467-7openalex-snapshot
A salvage pathway maintains highly functional respiratory complex I
inferredcites →https://doi.org/10.1046/j.1365-2958.2003.03524.xopenalex-snapshot
Alternative roles of ClpX and ClpP in Staphylococcus aureus stress tolerance and virulence
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/10.1046/j.1365-313x.2001.01108.xopenalex-snapshot
Mutagenesis and computer modelling approach to study determinants for recognition of signal peptides by the mitochondrial processing peptidase
inferredcites →https://doi.org/10.1074/jbc.m112.432070openalex-snapshot
Subcomplexes of Ancestral Respiratory Complex I Subunits Rapidly Turn Over in Vivo as Productive Assembly Intermediates in Arabidopsis*
inferredcites →https://doi.org/10.1074/jbc.m309212200openalex-snapshot
Clp Protease Complexes from Photosynthetic and Non-photosynthetic Plastids and Mitochondria of Plants, Their Predicted Three-dimensional Structures, and Functional Implications
inferredcites →https://doi.org/10.1074/mcp.m400129-mcp200openalex-snapshot
Multiplexed Protein Quantitation in Saccharomyces cerevisiae Using Amine-reactive Isobaric Tagging Reagents
inferredcites →https://doi.org/10.1074/mcp.m700535-mcp200openalex-snapshot
Heterogeneity of the Mitochondrial Proteome for Photosynthetic and Non-photosynthetic Arabidopsis Metabolism
inferredcites →https://doi.org/10.1074/mcp.m900104-mcp200openalex-snapshot
Large Scale Comparative Proteomics of a Chloroplast Clp Protease Mutant Reveals Folding Stress, Altered Protein Homeostasis, and Feedback Regulation of Metabolism
inferredcites →https://doi.org/10.1093/bioinformatics/btu743openalex-snapshot
CRISPRdirect: software for designing CRISPR/Cas guide RNA with reduced off-target sites
inferredcites →https://doi.org/10.1093/embo-reports/kvd024openalex-snapshot
RNA degradation buffers asymmetries of transcription in Arabidopsis mitochondria
inferredcites →https://doi.org/10.1093/hmg/ddt338openalex-snapshot
Loss of mitochondrial peptidase Clpp leads to infertility, hearing loss plus growth retardation via accumulation of CLPX, mtDNA and inflammatory factors
inferredcites →https://doi.org/10.1093/jxb/erx066openalex-snapshot
Generation and characterization of a collection of knock-down lines for the chloroplast Clp protease complex in tobacco
inferredcites →https://doi.org/10.1093/nar/19.6.1349openalex-snapshot
A simple and rapid method for the preparation of plant genomic DNA for PCR analysis
inferredcites →https://doi.org/10.1093/nar/gks119openalex-snapshot
Subscriptions
inferredcites →https://doi.org/10.1093/nar/gks1193openalex-snapshot
NCBI GEO: archive for functional genomics data sets—update
inferredcites →https://doi.org/10.1093/nar/gkw1129openalex-snapshot
CDD/SPARCLE: functional classification of proteins via subfamily domain architectures
inferredcites →https://doi.org/10.1093/nar/gky1106openalex-snapshot
The PRIDE database and related tools and resources in 2019: improving support for quantification data
inferredcites →https://doi.org/10.1093/nar/gky995openalex-snapshot
The Pfam protein families database in 2019
inferredcites →https://doi.org/10.1093/pcp/pce031openalex-snapshot
The Chloroplast clpP Gene, Encoding a Proteolytic Subunit of ATP-Dependent Protease, is Indispensable for Chloroplast Development in Tobacco
inferredcites →https://doi.org/10.1093/pcp/pcm052openalex-snapshot
Multiple Intracellular Locations of Lon Protease in Arabidopsis: Evidence for the Localization of AtLon4 to Chloroplasts
inferredcites →https://doi.org/10.1099/00221287-148-7-2255openalex-snapshot
The clpP multigene family for the ATP-dependent Clp protease in the cyanobacterium Synechococcus c cThe GenBank accession numbers for the sequences of clpPII-clpX and clpR-clpPIII reported in this paper are U92039 and AJ132005, respectively.
inferredcites →https://doi.org/10.1104/pp.112.197525openalex-snapshot
Chloroplast RH3 DEAD Box RNA Helicases in Maize and Arabidopsis Function in Splicing of Specific Group II Introns and Affect Chloroplast Ribosome Biogenesis
inferredcites →https://doi.org/10.1104/pp.112.203711openalex-snapshot
Loss of Lon1 in Arabidopsis Changes the Mitochondrial Proteome Leading to Altered Metabolite Profiles and Growth Retardation without an Accumulation of Oxidative Damage
inferredcites →https://doi.org/10.1104/pp.113.215699openalex-snapshot
Modified Clp Protease Complex in the ClpP3 Null Mutant and Consequences for Chloroplast Development and Function in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.113.217604openalex-snapshot
A Rice Virescent-Yellow Leaf Mutant Reveals New Insights into the Role and Assembly of Plastid Caseinolytic Protease in Higher Plants
inferredcites →https://doi.org/10.1104/pp.114.243014openalex-snapshot
Proteins with High Turnover Rate in Barley Leaves Estimated by Proteome Analysis Combined with in Planta Isotope Labeling
inferredcites →https://doi.org/10.1104/pp.16.00166openalex-snapshot
The Roles of Mitochondrial Reactive Oxygen Species in Cellular Signaling and Stress Response in Plants
inferredcites →https://doi.org/10.1104/pp.16.00370openalex-snapshot
Lack of FTSH4 Protease Affects Protein Carbonylation, Mitochondrial Morphology, and Phospholipid Content in Mitochondria of Arabidopsis: New Insights into a Complex Interplay
inferredcites →https://doi.org/10.1104/pp.17.01635openalex-snapshot
Temporal Proteomics of Inducible RNAi Lines of Clp Protease Subunits Identifies Putative Protease Substrates
inferredcites →https://doi.org/10.1104/pp.19.00822openalex-snapshot
A Mitochondrial LYR Protein Is Required for Complex I Assembly
inferredcites →https://doi.org/10.1105/tpc.10.7.1217openalex-snapshot
A Cytoplasmic Male Sterility–Associated Mitochondrial Peptide in Common Bean Is Post-Translationally Regulated
inferredcites →https://doi.org/10.1105/tpc.104.030254openalex-snapshot
Coordination of Nuclear and Mitochondrial Genome Expression during Mitochondrial Biogenesis in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.106.042861openalex-snapshot
Downregulation of ClpR2 Leads to Reduced Accumulation of the ClpPRS Protease Complex and Defects in Chloroplast Biogenesis in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.106.044594openalex-snapshot
Structural and Functional Insights into the Chloroplast ATP-Dependent Clp Protease in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.108.063784openalex-snapshot
Subunits of the Plastid ClpPR Protease Complex Have Differential Contributions to Embryogenesis, Plastid Biogenesis, and Plant Development inArabidopsis
inferredcites →https://doi.org/10.1105/tpc.109.068536openalex-snapshot
Phage-Type RNA Polymerase RPOTmp Performs Gene-Specific Transcription in Mitochondria of Arabidopsis thaliana
inferredcites →https://doi.org/10.1111/j.1399-3054.2011.01531.xopenalex-snapshot
A novel mitochondrial and chloroplast peptidasome, PreP
inferredcites →https://doi.org/10.1111/j.1432-1033.1992.tb17245.xopenalex-snapshot
Affinity purification of cytochrome c reductase from potato mitochondria
inferredcites →https://doi.org/10.1111/j.1469-8137.2008.02701.xopenalex-snapshot
Role of Lon1 protease in post‐germinative growth and maintenance of mitochondrial function in Arabidopsis thaliana
inferredcites →https://doi.org/10.1111/tpj.13392openalex-snapshot
Changes in specific protein degradation rates in Arabidopsis thaliana reveal multiple roles of Lon1 in mitochondrial protein homeostasis
inferredcites →https://doi.org/10.1111/tpj.13448openalex-snapshot
The mitochondrial complexome of Arabidopsis thaliana
inferredcites →https://doi.org/10.1111/tpj.14133openalex-snapshot
The assembly pathway of complex I in Arabidopsis thaliana
inferredcites →https://doi.org/10.1111/tpj.14293openalex-snapshot
The macrocyclizing protease butelase 1 remains autocatalytic and reveals the structural basis for ligase activity
inferredcites →https://doi.org/10.1128/jb.01233-07openalex-snapshot
Clp-Dependent Proteolysis Down-Regulates Central Metabolic Pathways in Glucose-Starved Bacillus subtilis
inferredcites →https://doi.org/10.1146/annurev-arplant-042110-103857openalex-snapshot
Organization and Regulation of Mitochondrial Respiration in Plants
inferredcites →https://doi.org/10.1146/annurev-arplant-043014-115547openalex-snapshot
Protein Maturation and Proteolysis in Plant Plastids, Mitochondria, and Peroxisomes
inferredcites →https://doi.org/10.1146/annurev-arplant-050718-100412openalex-snapshot
Assembly of the Complexes of the Oxidative Phosphorylation System in Land Plant Mitochondria
inferredcites →https://doi.org/10.1146/annurev.ge.24.120190.000515openalex-snapshot
CONTROL OF MITOCHONDRIAL GENE EXPRESSION IN SACCHAROMYCES CEREVISIAE
inferredcites →https://doi.org/10.1186/1746-4811-1-11openalex-snapshot
Blue-native PAGE in plants: a tool in analysis of protein-protein interactions
inferredcites →https://doi.org/10.1186/s13059-014-0550-8openalex-snapshot
Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2
inferredcites →https://doi.org/10.1186/s13059-015-0715-0openalex-snapshot
Egg cell-specific promoter-controlled CRISPR/Cas9 efficiently generates homozygous mutants for multiple target genes in Arabidopsis in a single generation
inferredcites →https://doi.org/10.12688/f1000research.15872.1openalex-snapshot
The evolution and diversity of the nonsense-mediated mRNA decay pathway
inferredcites →https://doi.org/10.15252/embj.201694253openalex-snapshot
CLPP coordinates mitoribosomal assembly through the regulation of ERAL1 levels
inferredcites →https://doi.org/10.2174/1389202911314020003openalex-snapshot
Integrated Analysis of Transcriptomic and Proteomic Data

What points at this work

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

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The Dynamic Shift in Mitochondria from Mature Pollen Grains
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Plant Proteolysis in Development: Insights and Functions
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Role of Mitochondria in Mechanisms of Fungal Senescence and Longevity
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Molecular chaperones, proteases, and unfolded protein responses
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Seed mitochondria are equipped with cristae and a full proteome to kickstart germination
inferred← citeshttps://doi.org/10.1016/j.mito.2020.04.011openalex-snapshot
Protein turnover rates in plant mitochondria
inferred← citeshttps://doi.org/10.1038/s41477-022-01165-3openalex-snapshot
Metabolic evidence for distinct pyruvate pools inside plant mitochondria
inferred← citeshttps://doi.org/10.1042/bcj20250120openalex-snapshot
Proteolytic coordination of the OXPHOS Life Cycle
inferred← citeshttps://doi.org/10.1042/bst20220195openalex-snapshot
Proteolytic regulation of mitochondrial oxidative phosphorylation components in plants
inferred← citeshttps://doi.org/10.1080/15592324.2020.1831789openalex-snapshot
Loss of conserved mitochondrial CLPP and its functions lead to different phenotypes in plants and other organisms
inferred← citeshttps://doi.org/10.1089/ars.2023.0487openalex-snapshot
Impact of Mitochondrial Architecture, Function, Redox Homeostasis, and Quality Control on Organismic Aging: Lessons from a Fungal Model System
inferred← citeshttps://doi.org/10.1093/gbe/evag007openalex-snapshot
Correlated Evolutionary Rates Reveal Novel Components and Cross-Compartment Connectivity in Plant Proteostasis Systems
inferred← citeshttps://doi.org/10.1093/pcp/pcaf038openalex-snapshot
Mitochondrial proteases and their roles in mitophagy in plants, animals, and yeast
inferred← citeshttps://doi.org/10.1093/plcell/koab148openalex-snapshot
The mitochondrial pyruvate carrier (MPC) complex mediates one of three pyruvate-supplying pathways that sustain Arabidopsis respiratory metabolism
inferred← citeshttps://doi.org/10.1093/plcell/koad128openalex-snapshot
FTSH PROTEASE 3 facilitates Complex I degradation through a direct interaction with the Complex I subunit PSST
inferred← citeshttps://doi.org/10.1093/plcell/koae141openalex-snapshot
Protein degrons and degradation: Exploring substrate recognition and pathway selection in plants
inferred← citeshttps://doi.org/10.1093/plcell/koae193openalex-snapshot
The lowdown on breakdown: Open questions in plant proteolysis
inferred← citeshttps://doi.org/10.1093/plcell/koae242openalex-snapshot
EARLY NODULIN93 acts via cytochrome c oxidase to alter respiratory ATP production and root growth in plants
inferred← citeshttps://doi.org/10.1093/plphys/kiab074openalex-snapshot
The mitochondrial AAA protease FTSH3 regulates Complex I abundance by promoting its disassembly
inferred← citeshttps://doi.org/10.1093/plphys/kiab101openalex-snapshot
Mitochondrial redox systems as central hubs in plant metabolism and signaling
inferred← citeshttps://doi.org/10.1093/plphys/kiab578openalex-snapshot
Alternative oxidase (AOX) 1a and 1d limit proline-induced oxidative stress and aid salinity recovery in Arabidopsis
inferred← citeshttps://doi.org/10.1093/plphys/kiad108openalex-snapshot
The biogenesis and regulation of the plant oxidative phosphorylation system
inferred← citeshttps://doi.org/10.1093/plphys/kiad233openalex-snapshot
Alternative oxidase 1a and 1d enable metabolic flexibility during Ala catabolism in Arabidopsis
inferred← citeshttps://doi.org/10.1093/plphys/kiae008openalex-snapshot
Mitochondrial atp1 mRNA knockdown by a custom-designed pentatricopeptide repeat protein alters ATP synthase
inferred← citeshttps://doi.org/10.1101/2022.11.08.515711openalex-snapshot
Knockdown of mitochondrial atp1 mRNA by a custom-designed pentatricopeptide repeat protein alters F 1 F o ATP synthase
inferred← citeshttps://doi.org/10.1101/2023.02.23.529725openalex-snapshot
FTSH3 facilitates complex I degradation through a direct interaction with the complex I subunit PSST
inferred← citeshttps://doi.org/10.1101/2023.04.15.535782openalex-snapshot
ENOD93 interacts with cytochrome c oxidase altering respiratory ATP production and root growth in plants
inferred← citeshttps://doi.org/10.1111/febs.15964openalex-snapshot
Mitochondrial matrix proteases: quality control and beyond
inferred← citeshttps://doi.org/10.1111/jipb.13958openalex-snapshot
Mitochondrial complex I assembles via a distal‐pump module (PD)‐early and PD‐late pathway in maize
inferred← citeshttps://doi.org/10.1111/pce.70322openalex-snapshot
Metabolic Responses to Salinity Identify a Role for Mitochondrial 2‐Oxoglutarate Dehydrogenase in Wheat Tissue Tolerance
inferred← citeshttps://doi.org/10.21248/gups.65210openalex-snapshot
Untersuchungen zur Bedeutung des mitochondrialen CLPXP-Komplexes für den Energie-Metabolismus von Podospora anserina
inferred← citeshttps://doi.org/10.3389/fcell.2021.616520openalex-snapshot
Simultaneous Ablation of the Catalytic AMPK α-Subunit SNF1 and Mitochondrial Matrix Protease CLPP Results in Pronounced Lifespan Extension
inferred← citeshttps://doi.org/10.3390/biom14020241openalex-snapshot
CLPP-Null Eukaryotes with Excess Heme Biosynthesis Show Reduced L-arginine Levels, Probably via CLPX-Mediated OAT Activation
inferred← citeshttps://doi.org/10.3390/ijms241713233openalex-snapshot
Alteration of Mitochondrial Transcript Expression in Arabidopsis thaliana Using a Custom-Made Library of Pentatricopeptide Repeat Proteins
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Exploring Cirrhosis: Insights into Advances in Therapeutic Strategies
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