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Arabidopsis pollen tube germination and growth depend on the mitochondrial calcium uniporter complex

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What this work says

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

inferredcites →https://doi.org/10.1007/s102650200020openalex-snapshot

The synergid cell: attractor and acceptor of the pollen tube for double fertilization

inferredcites →https://doi.org/10.1016/j.ab.2003.10.029openalex-snapshot

Ca2+ transport in mitochondria from yeast expressing recombinant aequorin

inferredcites →https://doi.org/10.1016/j.bbamcr.2012.10.009openalex-snapshot

Calcium - a central regulator of pollen germination and tube growth

inferredcites →https://doi.org/10.1016/j.celrep.2015.12.054openalex-snapshot

EMRE Is a Matrix Ca2+ Sensor that Governs Gatekeeping of the Mitochondrial Ca2+ Uniporter

inferredcites →https://doi.org/10.1016/j.cmet.2014.12.004openalex-snapshot

CCDC90A (MCUR1) Is a Cytochrome c Oxidase Assembly Factor and Not a Regulator of the Mitochondrial Calcium Uniporter

inferredcites →https://doi.org/10.1016/j.cub.2010.01.051openalex-snapshot

Arabidopsis Female Gametophyte Gene Expression Map Reveals Similarities between Plant and Animal Gametes

inferredcites →https://doi.org/10.1016/j.mito.2014.01.005openalex-snapshot

Role of mitochondria during female gametophyte development and fertilization in A. thaliana

inferredcites →https://doi.org/10.1016/j.molcel.2014.01.013openalex-snapshot

MICU1 and MICU2 Finely Tune the Mitochondrial Ca2+ Uniporter by Exerting Opposite Effects on MCU Activity

inferredcites →https://doi.org/10.1016/j.molp.2015.12.004openalex-snapshot

Ion Channels in Plant Bioenergetic Organelles, Chloroplasts and Mitochondria: From Molecular Identification to Function

inferredcites →https://doi.org/10.1016/j.pt.2011.10.007openalex-snapshot

Trypanosomes and the solution to a 50-year mitochondrial calcium mystery

inferredcites →https://doi.org/10.1016/j.semcdb.2016.07.024openalex-snapshot

Cell fusion and nuclear fusion in plants

inferredcites →https://doi.org/10.1016/j.tplants.2017.10.006openalex-snapshot

Capacitation in Plant and Animal Fertilization

inferredcites →https://doi.org/10.1038/emboj.2013.157openalex-snapshot

The mitochondrial calcium uniporter is a multimer that can include a dominant‐negative pore‐forming subunit

inferredcites →https://doi.org/10.1038/nature09358openalex-snapshot

MICU1 encodes a mitochondrial EF hand protein required for Ca2+ uptake

inferredcites →https://doi.org/10.1038/nature10230openalex-snapshot

A forty-kilodalton protein of the inner membrane is the mitochondrial calcium uniporter

inferredcites →https://doi.org/10.1038/nature10234openalex-snapshot

Integrative genomics identifies MCU as an essential component of the mitochondrial calcium uniporter

inferredcites →https://doi.org/10.1038/nature17656openalex-snapshot

Architecture of the mitochondrial calcium uniporter

inferredcites →https://doi.org/10.1038/ncb2622openalex-snapshot

MCUR1 is an essential component of mitochondrial Ca2+ uptake that regulates cellular metabolism

inferredcites →https://doi.org/10.1038/nrm4039openalex-snapshot

The molecular era of the mitochondrial calcium uniporter

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.1400514111openalex-snapshot

Reconstitution of the mitochondrial calcium uniporter in yeast

inferredcites →https://doi.org/10.1093/jxb/err394openalex-snapshot

Plant organellar calcium signalling: an emerging field

inferredcites →https://doi.org/10.1093/jxb/erw100openalex-snapshot

Regulation of mitochondrial calcium in plants versus animals

inferredcites →https://doi.org/10.1093/pcp/pcn084openalex-snapshot

Mitochondrial Dynamics in Plant Male Gametophyte Visualized by Fluorescent Live Imaging

inferredcites →https://doi.org/10.1104/pp.16.01359openalex-snapshot

Physiological Characterization of a Plant Mitochondrial Calcium Uniporter in Vitro and in Vivo

inferredcites →https://doi.org/10.1104/pp.16.01482openalex-snapshot

Gametophyte Development Needs Mitochondrial Coproporphyrinogen III Oxidase Function

inferredcites →https://doi.org/10.1104/pp.16.01561openalex-snapshot

Signaling with Ions: The Keystone for Apical Cell Growth and Morphogenesis in Pollen Tubes

inferredcites →https://doi.org/10.1105/tpc.15.00509openalex-snapshot

The EF-Hand Ca2+ Binding Protein MICU Choreographs Mitochondrial Ca2+ Dynamics in Arabidopsis

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/tpj.13448openalex-snapshot

The mitochondrial complexome of Arabidopsis thaliana

inferredcites →https://doi.org/10.1113/jphysiol.2013.268235openalex-snapshot

The mitochondrial calcium uniporter complex: molecular components, structure and physiopathological implications

inferredcites →https://doi.org/10.1126/science.1242993openalex-snapshot

EMRE Is an Essential Component of the Mitochondrial Calcium Uniporter Complex

inferredcites →https://doi.org/10.1128/mbio.00574-17openalex-snapshot

Different Roles of Mitochondrial Calcium Uniporter Complex Subunits in Growth and Infectivity of Trypanosoma cruzi

inferredcites →https://doi.org/10.1186/s13007-015-0099-xopenalex-snapshot

An improved method with a wider applicability to isolate plant mitochondria for mtDNA extraction

inferredcites →https://doi.org/10.1271/bbb.70216openalex-snapshot

Improved Gateway Binary Vectors: High-Performance Vectors for Creation of Fusion Constructs in Transgenic Analysis of Plants

inferredcites →https://doi.org/10.1371/journal.pone.0029685openalex-snapshot

A Powerful Method for Transcriptional Profiling of Specific Cell Types in Eukaryotes: Laser-Assisted Microdissection and RNA Sequencing

inferredcites →https://doi.org/10.1371/journal.pone.0055785openalex-snapshot

MICU2, a Paralog of MICU1, Resides within the Mitochondrial Uniporter Complex to Regulate Calcium Handling

inferredcites →https://doi.org/10.1515/biolog-2015-0077openalex-snapshot

Molecular characterization and phylogenetic analysis of ZmMCUs in maize

inferredcites →https://doi.org/10.3732/ajb.94.6.1046openalex-snapshot

Calcium function and distribution during fertilization in angiosperms

inferredcites →https://doi.org/10.7554/elife.15545openalex-snapshot

Dual functions of a small regulatory subunit in the mitochondrial calcium uniporter complex

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/s00709-018-1316-zopenalex-snapshot

In situ assessment of mitochondrial calcium transport in tobacco pollen tubes

inferred← citeshttps://doi.org/10.1007/s00709-026-02161-6openalex-snapshot

Cytological aspects of pollen germination in Mauritia flexuosa (Arecaceae)

inferred← citeshttps://doi.org/10.1007/s11816-025-00985-xopenalex-snapshot

Genome‑wide identification of the MCU gene family and expression analysis during Ralstonia solanacearum infection in Nicotiana tabacum L

inferred← citeshttps://doi.org/10.1007/s44154-026-00314-4openalex-snapshot

Perturbation of mitochondrial Ca2+ homeostasis activates cross-compartmental proteostatic response in Arabidopsis

inferred← citeshttps://doi.org/10.1016/b978-0-12-821792-4.00023-0openalex-snapshot

Calcium transport systems in chloroplasts and mitochondria of plant cells

inferred← citeshttps://doi.org/10.1016/j.bbabio.2020.148288openalex-snapshot

Mitochondrial calcium transport and permeability transition as rational targets for plant protection

inferred← citeshttps://doi.org/10.1016/j.bbabio.2022.148586openalex-snapshot

Morphology and permeability transitions in plant mitochondria: Different aspects of the same event?

inferred← citeshttps://doi.org/10.1016/j.cell.2026.08.027openalex-snapshot

A high-confidence plant mitochondrial proteome via protein correlation profiling

inferred← citeshttps://doi.org/10.1016/j.cj.2024.01.014openalex-snapshot

Suppressing a mitochondrial calcium uniporter activates the calcium signaling pathway and promotes cell elongation in cotton

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/10.1016/j.jplph.2022.153792openalex-snapshot

Regulation of pollen tube growth by cellular pH and ions

inferred← citeshttps://doi.org/10.1016/j.jprot.2023.104867openalex-snapshot

The triticale mature pollen and stigma proteomes – assembling the proteins for a productive encounter

inferred← citeshttps://doi.org/10.1016/j.mex.2019.07.023openalex-snapshot

A simple method for mitochondrial respiration and calcium uptake assessment in pollen tubes

inferred← citeshttps://doi.org/10.1016/j.mito.2020.05.007openalex-snapshot

Channels and transporters for inorganic ions in plant mitochondria: Prediction and facts

inferred← citeshttps://doi.org/10.1016/j.pharmthera.2018.07.001openalex-snapshot

Mitochondrial Ca2+ signaling

inferred← citeshttps://doi.org/10.1016/j.plantsci.2024.112227openalex-snapshot

Optimizing pollen germination and subcellular dynamics in pollen tube of Torreya grandis

inferred← citeshttps://doi.org/10.1016/j.plaphy.2025.110180openalex-snapshot

Exploration of mitochondrial calcium uniporters suggested their role in abiotic stress response in bread wheat

inferred← citeshttps://doi.org/10.1016/j.scienta.2021.110693openalex-snapshot

Characterization of self-incompatibility and expression profiles of CsMCU2 related to pollination in different varieties of tea plants

inferred← citeshttps://doi.org/10.1017/qpb.2020.4openalex-snapshot

Mitochondrial dynamics and segregation during the asymmetric division of Arabidopsis zygotes

inferred← citeshttps://doi.org/10.1017/qpb.2020.4.pr1openalex-snapshot

Author comment: Mitochondrial dynamics and segregation during the asymmetric division of Arabidopsis zygotes — R0/PR1

inferred← citeshttps://doi.org/10.1017/qpb.2020.4.pr10openalex-snapshot

Decision: Mitochondrial dynamics and segregation during the asymmetric division of Arabidopsis zygotes — R1/PR10

inferred← citeshttps://doi.org/10.1017/qpb.2020.4.pr2openalex-snapshot

Review: Mitochondrial dynamics and segregation during the asymmetric division of Arabidopsis zygotes — R0/PR2

inferred← citeshttps://doi.org/10.1017/qpb.2020.4.pr3openalex-snapshot

Review: Mitochondrial dynamics and segregation during the asymmetric division of Arabidopsis zygotes — R0/PR3

inferred← citeshttps://doi.org/10.1017/qpb.2020.4.pr4openalex-snapshot

Recommendation: Mitochondrial dynamics and segregation during the asymmetric division of Arabidopsis zygotes — R0/PR4

inferred← citeshttps://doi.org/10.1017/qpb.2020.4.pr5openalex-snapshot

Decision: Mitochondrial dynamics and segregation during the asymmetric division of Arabidopsis zygotes — R0/PR5

inferred← citeshttps://doi.org/10.1017/qpb.2020.4.pr6openalex-snapshot

Author comment: Mitochondrial dynamics and segregation during the asymmetric division of Arabidopsis zygotes — R1/PR6

inferred← citeshttps://doi.org/10.1017/qpb.2020.4.pr7openalex-snapshot

Review: Mitochondrial dynamics and segregation during the asymmetric division of Arabidopsis zygotes — R1/PR7

inferred← citeshttps://doi.org/10.1017/qpb.2020.4.pr8openalex-snapshot

Review: Mitochondrial dynamics and segregation during the asymmetric division of Arabidopsis zygotes — R1/PR8

inferred← citeshttps://doi.org/10.1017/qpb.2020.4.pr9openalex-snapshot

Recommendation: Mitochondrial dynamics and segregation during the asymmetric division of Arabidopsis zygotes — R1/PR9

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Genome-wide transcriptome analysis of the orphan crop tef (Eragrostis tef (Zucc.) Trotter) under long-term low calcium stress

inferred← citeshttps://doi.org/10.1080/00173134.2019.1637453openalex-snapshot

Calcium snapshots in the stigma and style of medlar (Lycium barbarum L.) during pollen germination and pollen tube growth suggest active calcium oscilations

inferred← citeshttps://doi.org/10.1080/15592324.2023.2271799openalex-snapshot

An Arabidopsis mutant line lacking the mitochondrial calcium transport regulator MICU shows an altered metabolite profile

inferred← citeshttps://doi.org/10.1089/bioe.2023.0002openalex-snapshot

Mitochondria–Chloroplast Cross Talk: A Possible Role for Calcium and Reactive Oxygen Species?

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The contribution of organelles to plant intracellular calcium signalling

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MCU proteins dominate in vivo mitochondrial Ca2+ uptake in Arabidopsis roots

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/kiab122openalex-snapshot

Transport, functions, and interaction of calcium and manganese in plant organellar compartments

inferred← citeshttps://doi.org/10.1093/plphys/kiab189openalex-snapshot

The signatures of organellar calcium

inferred← citeshttps://doi.org/10.1101/2022.10.02.510489openalex-snapshot

Perturbation of mitochondrial Ca 2+ homeostasis activates cross-compartmental proteostatic response in Arabidopsis

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Long‐term climate warming and nitrogen deposition increase leaf epiphytic and endophytic bacterial diversity

inferred← citeshttps://doi.org/10.1134/s1990747819030127openalex-snapshot

Taxonomic Features of Specific Ca2+ Transport Mechanisms in Mitochondria

inferred← citeshttps://doi.org/10.3389/fpls.2019.00389openalex-snapshot

Translocase of the Outer Mitochondrial Membrane 40 Is Required for Mitochondrial Biogenesis and Embryo Development in Arabidopsis

inferred← citeshttps://doi.org/10.3389/fpls.2020.00186openalex-snapshot

Chloroplast Calcium Signaling in the Spotlight

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The Role of Calcium/Calcium-Dependent Protein Kinases Signal Pathway in Pollen Tube Growth

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Comparative transcriptomic analysis of normal and abnormal in vitro flowers in Cymbidium nanulum Y. S. Wu et S. C. Chen identifies differentially expressed genes and candidate genes involved in flower formation

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Genome-Wide Identification of Wild Soybean Mitochondrial Calcium Uniporter Family Genes and Their Responses to Cold and Carbonate Alkaline Stresses

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Comparative analysis of wild-type and chloroplast MCU-deficient plants reveals multiple consequences of chloroplast calcium handling under drought stress

inferred← citeshttps://doi.org/10.3390/ijms19113370openalex-snapshot

Integration between ROS Regulatory Systems and Other Signals in the Regulation of Various Types of Heat Responses in Plants

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The Long Journey of Pollen Tube in the Pistil

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Genome-Wide Identification and Expression Profiling Analysis of the Mitochondrial Calcium Uniporter Gene Family Under Abiotic Stresses in Medicago sativa

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Signaling in Pollen Tube Growth: Beyond the Tip of the Polarity Iceberg

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