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Defensin-like polypeptide LUREs are pollen tube attractants secreted from synergid cells
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/7089_053openalex-snapshot
Comparative Analysis of Biological Models used in the Study of Pollen Tube Growth
inferredcites →https://doi.org/10.1007/s00253-006-0434-2openalex-snapshot
Promising nucleic acid analogs and mimics: characteristic features and applications of PNA, LNA, and morpholino
inferredcites →https://doi.org/10.1007/s00425-006-0283-3openalex-snapshot
EST generation and analyses towards identifying female gametophyte-specific genes in Zea mays L.
inferredcites →https://doi.org/10.1007/s004250000289openalex-snapshot
Symplastic communication between the central cell and the egg apparatus cells in the embryo sac of Torenia fournieri Lind. before and during fertilization
inferredcites →https://doi.org/10.1007/s00497-007-0059-3openalex-snapshot
Development and function of the synergid cell
inferredcites →https://doi.org/10.1007/s00497-007-0062-8openalex-snapshot
A comparison of early molecular fertilization mechanisms in animals and flowering plants
inferredcites →https://doi.org/10.1007/s00497-007-0064-6openalex-snapshot
Gametophytic pollen tube guidance
inferredcites →https://doi.org/10.1007/s004970050186openalex-snapshot
Isolation and osmotic relations of developing megagametophytes of Torenia fournieri
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.cub.2007.05.019openalex-snapshot
Distinct Dynamics of HISTONE3 Variants between the Two Fertilization Products in Plants
inferredcites →https://doi.org/10.1016/j.tplants.2008.05.011openalex-snapshot
Double fertilization – caught in the act
inferredcites →https://doi.org/10.1016/s0092-8674(03)00479-3openalex-snapshot
Pollen Tube Growth and Guidance Is Regulated by POP2, an Arabidopsis Gene that Controls GABA Levels
inferredcites →https://doi.org/10.1016/s0969-2126(01)00177-0openalex-snapshot
Refined three-dimensional solution structure of insect defensin A
inferredcites →https://doi.org/10.1038/33929openalex-snapshot
Lipids are required for directional pollen-tube growth
inferredcites →https://doi.org/10.1038/35097104openalex-snapshot
Direct ligand–receptor complex interaction controls Brassica self-incompatibility
inferredcites →https://doi.org/10.1046/j.0960-7412.2000.00944.xopenalex-snapshot
ZmES genes encode peptides with structural homology to defensins and are specifically expressed in the female gametophyte of maize
inferredcites →https://doi.org/10.1073/pnas.0401567101openalex-snapshot
Multidimensional signatures in antimicrobial peptides
inferredcites →https://doi.org/10.1073/pnas.2533800100openalex-snapshot
Chemocyanin, a small basic protein from the lily stigma, induces pollen tube chemotropism
inferredcites →https://doi.org/10.1104/pp.105.060079openalex-snapshot
Genome Organization of More Than 300 Defensin-Like Genes in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.106.083832openalex-snapshot
Species Preferentiality of the Pollen Tube Attractant Derived from the Synergid Cell ofTorenia fournieri
inferredcites →https://doi.org/10.1105/tpc.10.12.2019openalex-snapshot
Guidance in Vitro of the Pollen Tube to the Naked Embryo Sac of Torenia fournieri
inferredcites →https://doi.org/10.1105/tpc.10.8.1333openalex-snapshot
PCP-A1, a Defensin-like Brassica Pollen Coat Protein That Binds the S Locus Glycoprotein, Is the Product of Gametophytic Gene Expression
inferredcites →https://doi.org/10.1105/tpc.105.034603openalex-snapshot
MYB98Is Required for Pollen Tube Guidance and Synergid Cell Differentiation inArabidopsis
inferredcites →https://doi.org/10.1105/tpc.107.052076openalex-snapshot
MYB98 Positively Regulates a Battery of Synergid-Expressed Genes Encoding Filiform Apparatus–Localized Proteins
inferredcites →https://doi.org/10.1105/tpc.12.1.151openalex-snapshot
A Lipid Transfer–like Protein Is Necessary for Lily Pollen Tube Adhesion to an in Vitro Stylar Matrix
inferredcites →https://doi.org/10.1111/j.1365-313x.2005.02332.xopenalex-snapshot
The transcript composition of egg cells changes significantly following fertilization in wheat (Triticum aestivum L.)
inferredcites →https://doi.org/10.1111/j.1365-313x.2007.03136.xopenalex-snapshot
Small cysteine‐rich peptides resembling antimicrobial peptides have been under‐predicted in plants
inferredcites →https://doi.org/10.1126/science.1062429openalex-snapshot
Pollen Tube Attraction by the Synergid Cell
inferredcites →https://doi.org/10.1126/science.1065051openalex-snapshot
Pollen Tube Guidance--Right on Target
inferredcites →https://doi.org/10.1126/science.1104954openalex-snapshot
Micropylar Pollen Tube Guidance by Egg Apparatus 1 of Maize
inferredcites →https://doi.org/10.1126/science.1143562openalex-snapshot
The FERONIA Receptor-like Kinase Mediates Male-Female Interactions During Pollen Tube Reception
inferredcites →https://doi.org/10.1371/journal.pgen.0030171openalex-snapshot
Genome-Wide Expression Profiling of the Arabidopsis Female Gametophyte Identifies Families of Small, Secreted Proteins
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Mobile Signaling Peptides: Secret Molecular Messengers with a Mighty Role in Plant Life
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Overexpression of Arabidopsis miR157b induces bushy architecture and delayed phase transition in Torenia fournieri
inferred← citeshttps://doi.org/10.1007/s00425-020-03526-8openalex-snapshot
Glycosylphosphatidylinositol-anchored proteins mediate the interactions between pollen/pollen tube and pistil tissues
inferred← citeshttps://doi.org/10.1007/s00425-025-04648-7openalex-snapshot
Beyond the surface: the plant secretome as a bridge between the cell and its environment
inferred← citeshttps://doi.org/10.1007/s00438-015-1028-4openalex-snapshot
Rapid turnover of antimicrobial-type cysteine-rich protein genes in closely related Oryza genomes
inferred← citeshttps://doi.org/10.1007/s00468-014-1013-2openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00497-011-0161-4openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00497-011-0170-3openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00497-015-0272-4openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00497-016-0280-zopenalex-snapshot
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The SEEL motif and members of the MYB-related REVEILLE transcription factor family are important for the expression of LORELEI in the synergid cells of the Arabidopsis female gametophyte
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inferred← citeshttps://doi.org/10.1016/b978-0-12-801922-1.00004-xopenalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-12-821452-7.00004-0openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-443-15652-6.00001-1openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/bs.ctdb.2016.11.007openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/bs.ctdb.2018.11.013openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/bs.ctdb.2018.11.016openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/bs.ctdb.2024.10.009openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.aac.2023.01.003openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.bbamem.2015.10.011openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.bbapap.2013.03.024openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.bbrc.2019.11.028openalex-snapshot
Establishment of a novel method for the identification of fertilization defective mutants in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1016/j.cell.2023.06.024openalex-snapshot
Central-cell-produced attractants control fertilization recovery
inferred← citeshttps://doi.org/10.1016/j.celrep.2025.115390openalex-snapshot
Sexual reproduction in plants under high temperature and drought stress
inferred← citeshttps://doi.org/10.1016/j.celrep.2025.115815openalex-snapshot
Brassinosteroids promote pollen tube guidance by coordinating gene expression in male and female reproductive tissues
inferred← citeshttps://doi.org/10.1016/j.crvi.2010.01.009openalex-snapshot
Specificities of plant development
inferred← citeshttps://doi.org/10.1016/j.cub.2009.06.018openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.cub.2009.06.049openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.cub.2010.01.051openalex-snapshot
Arabidopsis Female Gametophyte Gene Expression Map Reveals Similarities between Plant and Animal Gametes
inferred← citeshttps://doi.org/10.1016/j.cub.2010.06.038openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.cub.2010.09.040openalex-snapshot
Signaling and Transcriptional Control of Reproductive Development in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.cub.2011.02.013openalex-snapshot
Live-Cell Imaging Reveals the Dynamics of Two Sperm Cells during Double Fertilization in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1016/j.cub.2012.03.069openalex-snapshot
Fertilization Recovery after Defective Sperm Cell Release in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.cub.2012.04.041openalex-snapshot
Gamete Fusion Is Required to Block Multiple Pollen Tubes from Entering an Arabidopsis Ovule
inferred← citeshttps://doi.org/10.1016/j.cub.2012.04.048openalex-snapshot
Plant Fertilization: Maximizing Reproductive Success
inferred← citeshttps://doi.org/10.1016/j.cub.2012.04.061openalex-snapshot
Overcoming Hybridization Barriers by the Secretion of the Maize Pollen Tube Attractant ZmEA1 from Arabidopsis Ovules
inferred← citeshttps://doi.org/10.1016/j.cub.2012.06.003openalex-snapshot
Plant Reproduction: Teaching a New Language of Love
inferred← citeshttps://doi.org/10.1016/j.cub.2013.04.043openalex-snapshot
Membrane-Bound RLCKs LIP1 and LIP2 Are Essential Male Factors Controlling Male-Female Attraction in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.cub.2013.05.021openalex-snapshot
Three MYB Transcription Factors Control Pollen Tube Differentiation Required for Sperm Release
inferred← citeshttps://doi.org/10.1016/j.cub.2013.10.019openalex-snapshot
Vision and the light environment
inferred← citeshttps://doi.org/10.1016/j.cub.2013.11.030openalex-snapshot
Gamete Attachment Requires GEX2 for Successful Fertilization in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.cub.2015.12.032openalex-snapshot
Fertilization Mechanisms in Flowering Plants
inferred← citeshttps://doi.org/10.1016/j.cub.2016.02.040openalex-snapshot
The AMOR Arabinogalactan Sugar Chain Induces Pollen-Tube Competency to Respond to Ovular Guidance
inferred← citeshttps://doi.org/10.1016/j.cub.2016.06.053openalex-snapshot
Maternal ENODLs Are Required for Pollen Tube Reception in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.cub.2020.09.006openalex-snapshot
Three STIGMA AND STYLE STYLISTs Pattern the Fine Architectures of Apical Gynoecium and Are Critical for Male Gametophyte-Pistil Interaction
inferred← citeshttps://doi.org/10.1016/j.cub.2022.11.044openalex-snapshot
Non-cell-autonomous small RNA silencing in Arabidopsis female gametes
inferred← citeshttps://doi.org/10.1016/j.cub.2024.10.025openalex-snapshot
Enhanced pollen tube performance at high temperature contributes to thermotolerant fruit and seed production in tomato
inferred← citeshttps://doi.org/10.1016/j.cub.2025.09.060openalex-snapshot
Arabidopsis LOHN1 peptide modulates lateral root spacing under the control of systemic nitrogen-satiety signaling
inferred← citeshttps://doi.org/10.1016/j.dci.2019.103556openalex-snapshot
Defensins: Transcriptional regulation and function beyond antimicrobial activity
inferred← citeshttps://doi.org/10.1016/j.devcel.2012.09.011openalex-snapshot
Mitochondrial GCD1 Dysfunction Reveals Reciprocal Cell-to-Cell Signaling during the Maturation of Arabidopsis Female Gametes
inferred← citeshttps://doi.org/10.1016/j.devcel.2015.07.007openalex-snapshot
Embryos, Camera, Laser, Action!
inferred← citeshttps://doi.org/10.1016/j.devcel.2021.09.026openalex-snapshot
Polarized NORTIA accumulation in response to pollen tube arrival at synergids promotes fertilization
inferred← citeshttps://doi.org/10.1016/j.devcel.2026.08.001openalex-snapshot
Functional versatility of synergid cells in plant reproduction
inferred← citeshttps://doi.org/10.1016/j.ejcb.2009.11.005openalex-snapshot
Analyzing female gametophyte development and function: There is more than one way to crack an egg
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2009.09.004openalex-snapshot
Cold stress effects on reproductive development in grain crops: An overview
inferred← citeshttps://doi.org/10.1016/j.fbr.2012.07.002openalex-snapshot
Antifungal proteins: More than antimicrobials?
inferred← citeshttps://doi.org/10.1016/j.fbr.2012.08.004openalex-snapshot
Plant defensins: Common fold, multiple functions
inferred← citeshttps://doi.org/10.1016/j.fbr.2012.10.002openalex-snapshot
Modes of antifungal action and in planta functions of plant defensins and defensin-like peptides
inferred← citeshttps://doi.org/10.1016/j.gene.2023.147328openalex-snapshot
Peptide signaling in anther development and pollen-stigma interactions
inferred← citeshttps://doi.org/10.1016/j.jbiosc.2015.03.021openalex-snapshot
Quantification of pollen tube attraction in response to guidance by female gametophyte tissue using artificial microscale pathway
inferred← citeshttps://doi.org/10.1016/j.jbiotec.2018.08.012openalex-snapshot
Localized expression of antimicrobial proteins mitigates huanglongbing symptoms in Mexican lime
inferred← citeshttps://doi.org/10.1016/j.jgg.2025.01.007openalex-snapshot
S-sulfenylation-mediated inhibition of the GSNOR1 activity regulates ovule development in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.mee.2014.01.017openalex-snapshot
Growth assay of individual pollen tubes arrayed by microchannel device
inferred← citeshttps://doi.org/10.1016/j.mib.2010.12.010openalex-snapshot
Peptide signalling in the rhizobium–legume symbiosis
inferred← citeshttps://doi.org/10.1016/j.molp.2016.01.002openalex-snapshot
“Love Is Strong, and You're so Sweet”: JAGGER Is Essential for Persistent Synergid Degeneration and Polytubey Block in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1016/j.molp.2018.02.010openalex-snapshot
Time Bomb for Pollen Tubes: Peptide RALF-Mediated Signaling
inferred← citeshttps://doi.org/10.1016/j.molp.2021.11.015openalex-snapshot
Dual and opposing roles of EIN3 reveal a generation conflict during seed growth
inferred← citeshttps://doi.org/10.1016/j.molp.2026.08.010openalex-snapshot
Stigmatic papilla cells secrete jasmonic acid to promote pollen germination through calcium signaling
inferred← citeshttps://doi.org/10.1016/j.pbi.2009.09.015openalex-snapshot
Micropylar pollen tube guidance and burst: adapted from defense mechanisms?
inferred← citeshttps://doi.org/10.1016/j.pbi.2010.06.002openalex-snapshot
Complex signals for simple cells: the expanding ranks of signals and receptors guiding stomatal development
inferred← citeshttps://doi.org/10.1016/j.pbi.2010.09.001openalex-snapshot
Ovule development in Arabidopsis: progress and challenge
inferred← citeshttps://doi.org/10.1016/j.pbi.2011.07.010openalex-snapshot
Attraction of tip-growing pollen tubes by the female gametophyte
inferred← citeshttps://doi.org/10.1016/j.pbi.2011.07.012openalex-snapshot
She's the boss: signaling in pollen tube reception
inferred← citeshttps://doi.org/10.1016/j.pbi.2012.07.003openalex-snapshot
CrRLK1L receptor-like kinases: not just another brick in the wall
inferred← citeshttps://doi.org/10.1016/j.pbi.2012.12.001openalex-snapshot
Cell-specific expression profiling of rare cell types as exemplified by its impact on our understanding of female gametophyte development
inferred← citeshttps://doi.org/10.1016/j.pbi.2013.08.005openalex-snapshot
Speed dating, rejection, and finding the perfect mate: advice from flowering plants
inferred← citeshttps://doi.org/10.1016/j.pbi.2013.12.005openalex-snapshot
Fertile approaches to dissecting mechanisms of premating and postmating prezygotic reproductive isolation
inferred← citeshttps://doi.org/10.1016/j.pbi.2014.07.011openalex-snapshot
Endogenous peptide ligand–receptor systems for diverse signaling networks in plants
inferred← citeshttps://doi.org/10.1016/j.pbi.2015.10.006openalex-snapshot
Peptide signaling in pollen tube guidance
inferred← citeshttps://doi.org/10.1016/j.pbi.2016.10.011openalex-snapshot
The end of temptation: the elimination of persistent synergid cell identity
inferred← citeshttps://doi.org/10.1016/j.pbi.2016.11.012openalex-snapshot
Polyspermy barriers: a plant perspective
inferred← citeshttps://doi.org/10.1016/j.pbi.2016.11.015openalex-snapshot
Cell polarity in plants: the Yin and Yang of cellular functions
inferred← citeshttps://doi.org/10.1016/j.pbi.2019.03.004openalex-snapshot
Peptide/receptor-like kinase-mediated signaling involved in male–female interactions
inferred← citeshttps://doi.org/10.1016/j.pbi.2019.05.011openalex-snapshot
Hormone-like peptides and small coding genes in plant stress signaling and development
inferred← citeshttps://doi.org/10.1016/j.pbi.2019.07.001openalex-snapshot
Structural biology of cell surface receptor–ligand interactions
inferred← citeshttps://doi.org/10.1016/j.pbi.2022.102271openalex-snapshot
Killing me softly - Programmed cell death in plant reproduction from sporogenesis to fertilization
inferred← citeshttps://doi.org/10.1016/j.peptides.2012.05.009openalex-snapshot
Discovery of novel antimicrobial peptides with unusual cysteine motifs in dandelion Taraxacum officinale Wigg. flowers
inferred← citeshttps://doi.org/10.1016/j.peptides.2021.170572openalex-snapshot
The role of diverse LURE-type cysteine-rich peptides as signaling molecules in plant reproduction
inferred← citeshttps://doi.org/10.1016/j.peptides.2021.170614openalex-snapshot
Molecular mechanisms of plant peptide binding to receptors
inferred← citeshttps://doi.org/10.1016/j.plantsci.2014.05.012openalex-snapshot
Multitasking antimicrobial peptides in plant development and host defense against biotic/abiotic stress
inferred← citeshttps://doi.org/10.1016/j.plantsci.2016.01.009openalex-snapshot
Molecular and cellular characterization of GA-Stimulated Transcripts GASA4 and GASA6 in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1016/j.plantsci.2018.09.002openalex-snapshot
A novel cysteine-rich peptide regulates cell expansion in the tobacco pistil and influences its final size
inferred← citeshttps://doi.org/10.1016/j.plantsci.2025.112436openalex-snapshot
Advances in research on the control of pollen tube growth by calcium in higher plants
inferred← citeshttps://doi.org/10.1016/j.plaphy.2020.11.052openalex-snapshot
The regulatory framework of developmentally programmed cell death in floral organs: A review
inferred← citeshttps://doi.org/10.1016/j.plaphy.2026.111187openalex-snapshot
Genome-wide identification and functional characterization of OsLAT52 genes associated with pollen tube growth in rice (Oryza sativa)
inferred← citeshttps://doi.org/10.1016/j.pmpp.2025.102814openalex-snapshot
Marine macroalgae (Ulva fasciata) and endophytic fungi enhance biotic stress-tolerance in Helianthus annuus L. by up-regulating the expression of stressor proteins
inferred← citeshttps://doi.org/10.1016/j.resmic.2011.02.005openalex-snapshot
Natural roles of antimicrobial peptides in microbes, plants and animals
inferred← citeshttps://doi.org/10.1016/j.scib.2018.02.010openalex-snapshot
The secret of fertilization in flowering plants unveiled
inferred← citeshttps://doi.org/10.1016/j.semcdb.2011.06.004openalex-snapshot
Rapid tip growth: Insights from pollen tubes
inferred← citeshttps://doi.org/10.1016/j.tcb.2009.12.007openalex-snapshot
Is HAP2-GCS1 an ancestral gamete fusogen?
inferred← citeshttps://doi.org/10.1016/j.tplants.2010.04.005openalex-snapshot
Under pressure, cell walls set the pace
inferred← citeshttps://doi.org/10.1016/j.tplants.2015.12.004openalex-snapshot
Understanding CrRLK1L Function: Cell Walls and Growth Control
inferred← citeshttps://doi.org/10.1016/j.tplants.2021.02.008openalex-snapshot
Peptide Signaling during Plant Reproduction
inferred← citeshttps://doi.org/10.1016/j.tplants.2025.08.021openalex-snapshot
Sustained cereal bowl amidst global warming
inferred← citeshttps://doi.org/10.1016/j.xplc.2023.100629openalex-snapshot
From the floret to the canopy: High temperature tolerance during flowering
inferred← citeshttps://doi.org/10.1016/j.xplc.2024.100934openalex-snapshot
Pollen-expressed RLCKs control pollen tube burst
inferred← citeshttps://doi.org/10.1016/j.xplc.2026.101915openalex-snapshot
Two transcription factors, MYB64 and MYB119, and their target cis-regulatory element control egg cell-specific gene expression in Arabidopsis
inferred← citeshttps://doi.org/10.1016/s0065-2296(09)51011-7openalex-snapshot
Chapter 11 Unexpected Turns and Twists in Structure/Function of PR-Proteins that Connect Energy Metabolism and Immunity
inferred← citeshttps://doi.org/10.1016/s0065-2296(10)54001-1openalex-snapshot
Pollen Germination and Tube Growth
inferred← citeshttps://doi.org/10.1016/s0070-2153(10)91013-2openalex-snapshot
Development of Flowering Plant Gametophytes
inferred← citeshttps://doi.org/10.1021/acs.jproteome.5b00618openalex-snapshot
The Plant Ovule Secretome: A Different View toward Pollen–Pistil Interactions
inferred← citeshttps://doi.org/10.1021/bk-2012-1095.ch013openalex-snapshot
Antimicrobial Peptides as a Promising Alternative for Plant Disease Protection
inferred← citeshttps://doi.org/10.1038/nature14561openalex-snapshot
Competitive binding of antagonistic peptides fine-tunes stomatal patterning
inferred← citeshttps://doi.org/10.1038/nature16975openalex-snapshot
A receptor heteromer mediates the male perception of female attractants in plants
inferred← citeshttps://doi.org/10.1038/nature17413openalex-snapshot
Tip-localized receptors control pollen tube growth and LURE sensing in Arabidopsis
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