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Monomeric G‐actin is uniformly distributed in pollen tubes and is rapidly redistributed via cytoplasmic streaming during pollen tube growth

https://doi.org/10.1111/tpj.13668
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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/(sici)1097-0169(1997)36:4<323::aid-cm3>3.0.co;2-6openalex-snapshot
Characterization and localization of profilin in pollen grains and tubes ofLilium longiflorum
inferredcites →https://doi.org/10.1002/cm.10013openalex-snapshot
Use of fluorescently labelled deoxyribonuclease I to spatially measure G‐actin levels in migrating and non‐migrating cells
inferredcites →https://doi.org/10.1002/cm.21160openalex-snapshot
Visualization of the actin cytoskeleton: Different F‐actin‐binding probes tell different stories
inferredcites →https://doi.org/10.1007/s004250100543openalex-snapshot
Circular F-actin bundles and a G-actin gradient in pollen and pollen tubes of Lilium davidii
inferredcites →https://doi.org/10.1007/s00709-006-0231-xopenalex-snapshot
The function of actin-binding proteins in pollen tube growth
inferredcites →https://doi.org/10.1007/s11103-006-9063-5openalex-snapshot
The late pollen actins are essential for normal male and female development in Arabidopsis
inferredcites →https://doi.org/10.1016/j.cell.2009.03.021openalex-snapshot
Structural Memory in the Contractile Ring Makes the Duration of Cytokinesis Independent of Cell Size
inferredcites →https://doi.org/10.1016/j.cub.2013.04.057openalex-snapshot
Dynamic Localization of G-Actin during Membrane Protrusion in Neuronal Motility
inferredcites →https://doi.org/10.1016/j.jsb.2011.10.005openalex-snapshot
Formins filter modified actin subunits during processive elongation
inferredcites →https://doi.org/10.1016/j.molcel.2006.01.016openalex-snapshot
Model of Formin-Associated Actin Filament Elongation
inferredcites →https://doi.org/10.1016/j.molp.2015.09.013openalex-snapshot
Profilin Regulates Apical Actin Polymerization to Control Polarized Pollen Tube Growth
inferredcites →https://doi.org/10.1016/j.molp.2017.05.002openalex-snapshot
Organizational Innovation of Apical Actin Filaments Drives Rapid Pollen Tube Growth and Turning
inferredcites →https://doi.org/10.1016/j.pbi.2006.09.013openalex-snapshot
Actin dynamics: old friends with new stories
inferredcites →https://doi.org/10.1016/j.pbi.2015.10.004openalex-snapshot
The cytoskeleton in the pollen tube
inferredcites →https://doi.org/10.1016/s0021-9258(17)36545-6openalex-snapshot
Jasplakinolide, a cytotoxic natural product, induces actin polymerization and competitively inhibits the binding of phalloidin to F-actin.
inferredcites →https://doi.org/10.1016/s0021-9258(19)85885-4openalex-snapshot
Vitamin D-binding protein (Gc-globulin) binds actin.
inferredcites →https://doi.org/10.1038/347037a0openalex-snapshot
Atomic structure of the actin: DNase I complex
inferredcites →https://doi.org/10.1038/nature09372openalex-snapshot
Direct visualization of secondary structures of F-actin by electron cryomicroscopy
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.1110109108openalex-snapshot
Remodeling of actin filaments by ADF/cofilin proteins
inferredcites →https://doi.org/10.1073/pnas.93.9.3886openalex-snapshot
Movement of yeast cortical actin cytoskeleton visualized in vivo.
inferredcites →https://doi.org/10.1074/jbc.275.7.5163openalex-snapshot
Effects of Jasplakinolide on the Kinetics of Actin Polymerization
inferredcites →https://doi.org/10.1083/jcb.123.1.173openalex-snapshot
Localization and dynamics of nonfilamentous actin in cultured cells [published erratum appears in J Cell Biol 1993 Nov;123(3):following 767]
inferredcites →https://doi.org/10.1083/jcb.131.6.1483openalex-snapshot
Actin filaments in yeast are unstable in the absence of capping protein or fimbrin.
inferredcites →https://doi.org/10.1083/jcb.200604011openalex-snapshot
Actin depolymerization is sufficient to induce programmed cell death in self-incompatible pollen
inferredcites →https://doi.org/10.1091/mbc.12.8.2534openalex-snapshot
Actin Polymerization Is Essential for Pollen Tube Growth
inferredcites →https://doi.org/10.1093/aob/mcl084openalex-snapshot
Distribution of G-actin is Related to Root Hair Growth of Wheat
inferredcites →https://doi.org/10.1093/emboj/cdf349openalex-snapshot
Involvement of the mitogen‐activated protein kinase SIMK in regulation of root hair tip growth
inferredcites →https://doi.org/10.1093/jxb/erq012openalex-snapshot
Regulation of actin dynamics by actin-binding proteins in pollen
inferredcites →https://doi.org/10.1093/jxb/erw160openalex-snapshot
Arabidopsis FIM5 decorates apical actin filaments and regulates their organization in the pollen tube
inferredcites →https://doi.org/10.1105/tpc.002998openalex-snapshot
Signal-Mediated Depolymerization of Actin in Pollen during the Self-Incompatibility Response
inferredcites →https://doi.org/10.1105/tpc.11.12.2349openalex-snapshot
Latrunculin B Has Different Effects on Pollen Germination and Tube Growth
inferredcites →https://doi.org/10.1105/tpc.110.076257openalex-snapshot
ArabidopsisVILLIN5, an Actin Filament Bundling and Severing Protein, Is Necessary for Normal Pollen Tube Growth
inferredcites →https://doi.org/10.1105/tpc.110.080283openalex-snapshot
Arabidopsis FIMBRIN5, an Actin Bundling Factor, Is Required for Pollen Germination and Pollen Tube Growth
inferredcites →https://doi.org/10.1105/tpc.113.117820openalex-snapshot
Arabidopsis ACTIN-DEPOLYMERIZING FACTOR7 Severs Actin Filaments and Regulates Actin Cable Turnover to Promote Normal Pollen Tube Growth
inferredcites →https://doi.org/10.1111/j.1550-7408.2003.tb00261.xopenalex-snapshot
Expression of GFP‐Actin Leads to Failure of Nuclear Elongation and Cytokinesis in Tetrahymena thermophila
inferredcites →https://doi.org/10.1111/j.1744-7909.2009.00850.xopenalex-snapshot
Regulation of Actin Dynamics in Pollen Tubes: Control of Actin Polymer Level
inferredcites →https://doi.org/10.1111/tpj.12910openalex-snapshot
Arabidopsis ACT 11 modifies actin turnover to promote pollen germination and maintain the normal rate of tube growth
inferredcites →https://doi.org/10.1126/science.1113230openalex-snapshot
Counting Cytokinesis Proteins Globally and Locally in Fission Yeast
inferredcites →https://doi.org/10.1146/annurev.arplant.59.032607.092921openalex-snapshot
Structural and Signaling Networks for the Polar Cell Growth Machinery in Pollen Tubes
inferredcites →https://doi.org/10.3389/fpls.2014.00786openalex-snapshot
Organization and regulation of the actin cytoskeleton in the pollen tube

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.4837604openalex-extracted
Dynamic Changes and Transcriptome Analyses Reveal the Microfilament Skeleton Response to Water Stress in Thalli of Neopyropia Yezoensis Inhabiting the Intertidal Zone
inferred← citeshttps://doi.org/10.1007/s11427-024-3067-yopenalex-snapshot
Cytoskeletal control of development and environmental adaptation in plants
inferred← citeshttps://doi.org/10.1016/j.stress.2025.100762openalex-snapshot
Dynamic changes and transcriptome analyses reveal the microfilament skeleton response to water stress in thalli of Neopyropia yezoensis inhabiting the intertidal zone
inferred← citeshttps://doi.org/10.1073/pnas.1821639116openalex-snapshot
Mechanism of CAP1-mediated apical actin polymerization in pollen tubes
inferred← citeshttps://doi.org/10.1091/mbc.e25-04-0171openalex-snapshot
Functional fluorescence labeling of actins in live-cell system using engineered split-GFP technology
inferred← citeshttps://doi.org/10.1093/pcp/pcz024openalex-snapshot
A Comparison of sun, ovate, fs8.1 and Auxin Application on Tomato Fruit Shape and Gene Expression
inferred← citeshttps://doi.org/10.1093/plphys/kiad203openalex-snapshot
Actin cytoskeleton in the control of vesicle transport, cytoplasmic organization, and pollen tube tip growth
inferred← citeshttps://doi.org/10.1093/plphys/kiae018openalex-snapshot
PLEIOTROPIC REGULATORY LOCUS1 maintains actin microfilament integrity to regulate pavement cell morphogenesis
inferred← citeshttps://doi.org/10.1101/2023.02.28.530536openalex-snapshot
PRL1 negatively regulates Rho GTPase-independent and - dependent signaling pathways maintaining actin microfilament dynamic for pavement cell morphogenesis
inferred← citeshttps://doi.org/10.1111/tpj.15723openalex-snapshot
Functional non‐equivalence of pollen ADF isovariants in Arabidopsis
inferred← citeshttps://doi.org/10.1360/ssv-2022-0183openalex-snapshot
Advances in the study of cytoskeleton system regulating pollen tube development
inferred← citeshttps://doi.org/10.1371/journal.pgen.1007789openalex-snapshot
Arabidopsis class I formins control membrane-originated actin polymerization at pollen tube tips
inferred← citeshttps://doi.org/10.3389/fcell.2020.614821openalex-snapshot
Control of the Actin Cytoskeleton Within Apical and Subapical Regions of Pollen Tubes
inferred← citeshttps://doi.org/10.3389/fpls.2021.599961openalex-snapshot
The Arabidopsis thaliana Class II Formin FH13 Modulates Pollen Tube Growth
inferred← citeshttps://doi.org/10.3390/plants12010008openalex-snapshot
Sterols and Sphingolipids as New Players in Cell Wall Building and Apical Growth of Nicotiana tabacum L. Pollen Tubes
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