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Photoperiodic Control of the Floral Transition through a Distinct Polycomb Repressive 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/bf00203657openalex-snapshot
The promoter of the Arabidopsis thaliana SUC2 sucrose-H+ symporter gene directs expression of ?-glucuronidase to the phloem: Evidence for phloem loading and unloading by SUC2
inferredcites →https://doi.org/10.1007/s00425-009-0958-7openalex-snapshot
Over-expression of CONSTANS-LIKE 5 can induce flowering in short-day grown Arabidopsis
inferredcites →https://doi.org/10.1016/j.cell.2006.02.041openalex-snapshot
A Bivalent Chromatin Structure Marks Key Developmental Genes in Embryonic Stem Cells
inferredcites →https://doi.org/10.1016/j.cub.2008.11.019openalex-snapshot
Polycomb Silencing of KNOX Genes Confines Shoot Stem Cell Niches in Arabidopsis
inferredcites →https://doi.org/10.1016/j.cub.2010.09.046openalex-snapshot
Keeping Cell Identity in Arabidopsis Requires PRC1 RING-Finger Homologs that Catalyze H2A Monoubiquitination
inferredcites →https://doi.org/10.1016/j.molcel.2012.01.002openalex-snapshot
PCGF Homologs, CBX Proteins, and RYBP Define Functionally Distinct PRC1 Family Complexes
inferredcites →https://doi.org/10.1038/cr.2010.151openalex-snapshot
The Arabidopsis PRC1-like ring-finger proteins are necessary for repression of embryonic traits during vegetative growth
inferredcites →https://doi.org/10.1038/cr.2010.27openalex-snapshot
JMJ14 is an H3K4 demethylase regulating flowering time in Arabidopsis
inferredcites →https://doi.org/10.1038/emboj.2013.145openalex-snapshot
Arabidopsis MSI1 connects LHP1 to PRC2 complexes
inferredcites →https://doi.org/10.1038/ncomms2947openalex-snapshot
Arabidopsis FLC clade members form flowering-repressor complexes coordinating responses to endogenous and environmental cues
inferredcites →https://doi.org/10.1038/nrm2763openalex-snapshot
Mechanisms of Polycomb gene silencing: knowns and unknowns
inferredcites →https://doi.org/10.1038/nsmb1283openalex-snapshot
The Arabidopsis LHP1 protein colocalizes with histone H3 Lys27 trimethylation
inferredcites →https://doi.org/10.1046/j.1365-313x.1994.6060903.xopenalex-snapshot
The late‐flowering phenotype of FRIGIDA and mutations in LUMINIDEPENDENS is suppressed in the Landsberg erecta strain of Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.1118678109openalex-snapshot
A core subunit of Polycomb repressive complex 1 is broadly conserved in function but not primary sequence
inferredcites →https://doi.org/10.1101/gad.373506openalex-snapshot
The transcription factor FLC confers a flowering response to vernalization by repressing meristem competence and systemic signaling in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.016345openalex-snapshot
TERMINAL FLOWER2, an Arabidopsis Homolog of HETEROCHROMATIN PROTEIN1, Counteracts the Activation of FLOWERING LOCUS T by CONSTANS in the Vascular Tissues of Leaves to Regulate Flowering Time
inferredcites →https://doi.org/10.1105/tpc.106.049957openalex-snapshot
EMBRYONIC FLOWER1 Participates in Polycomb Group–MediatedAGGene Silencing inArabidopsis
inferredcites →https://doi.org/10.1111/j.1365-313x.2006.02686.xopenalex-snapshot
The Arabidopsis FLC protein interacts directly in vivo with SOC1 and FT chromatin and is part of a high‐molecular‐weight protein complex
inferredcites →https://doi.org/10.1111/j.1469-8137.2010.03251.xopenalex-snapshot
The flowering time regulator CONSTANS is recruited to the FLOWERING LOCUS T promoter via a unique cis ‐element
inferredcites →https://doi.org/10.1126/science.1091761openalex-snapshot
Photoreceptor Regulation of CONSTANS Protein in Photoperiodic Flowering
inferredcites →https://doi.org/10.1146/annurev.arplant.59.032607.092755openalex-snapshot
Regulation and Identity of Florigen: FLOWERING LOCUS T Moves Center Stage
inferredcites →https://doi.org/10.1146/annurev.cellbio.042308.113411openalex-snapshot
Vernalization: Winter and the Timing of Flowering in Plants
inferredcites →https://doi.org/10.1186/1471-2148-8-294openalex-snapshot
Evolutionary history of histone demethylase families: distinct evolutionary patterns suggest functional divergence
inferredcites →https://doi.org/10.1186/gb-2009-10-6-r62openalex-snapshot
Genome-wide analysis of mono-, di- and trimethylation of histone H3 lysine 4 in Arabidopsis thaliana
inferredcites →https://doi.org/10.1371/journal.pgen.0030086openalex-snapshot
Arabidopsis TFL2/LHP1 Specifically Associates with Genes Marked by Trimethylation of Histone H3 Lysine 27
inferredcites →https://doi.org/10.1371/journal.pgen.1002512openalex-snapshot
EMF1 and PRC2 Cooperate to Repress Key Regulators of Arabidopsis Development
inferredcites →https://doi.org/10.1371/journal.pgen.1002664openalex-snapshot
A Companion Cell–Dominant and Developmentally Regulated H3K4 Demethylase Controls Flowering Time in Arabidopsis via the Repression of FLC Expression
inferredcites →https://doi.org/10.1371/journal.pone.0008033openalex-snapshot
Repression of FLOWERING LOCUS T Chromatin by Functionally Redundant Histone H3 Lysine 4 Demethylases in Arabidopsis
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.4788948openalex-extracted
Gmhsp40.1, a Nuclear-Localized Soybean Dnaj Domain-Containing Protein, Participates in Regulation of Flowering Time Through Interacting with Emf1 and Jmj14
inferred← citeshttps://doi.org/10.1002/9780470015902.a0023751openalex-snapshot
Plant Polycomb‐Group Proteins: Epigenetic Regulators of Development
inferred← citeshttps://doi.org/10.1002/advs.202204885openalex-snapshot
RNA 5‐Methylcytosine Modification Regulates Vegetative Development Associated with H3K27 Trimethylation in Arabidopsis
inferred← citeshttps://doi.org/10.1002/advs.202522307openalex-snapshot
Auto‐Downregulation of the Florigen FT Production Prevents Precocious Flowering in Plants
inferred← citeshttps://doi.org/10.1002/sstr.202000125openalex-snapshot
Regulation by FLOWERING LOCUS T and TERMINAL FLOWER 1 in Flowering Time and Plant Architecture
inferred← citeshttps://doi.org/10.1002/tpg2.20320openalex-snapshot
Epigenetic regulation of photoperiodic flowering in plants
inferred← citeshttps://doi.org/10.1007/978-1-4939-7318-7_13openalex-snapshot
Unraveling the Complex Epigenetic Mechanisms that Regulate Gene Activity
inferred← citeshttps://doi.org/10.1007/978-3-030-14760-0_8openalex-snapshot
Epigenetics of Light Signaling During Plant Development
inferred← citeshttps://doi.org/10.1007/978-3-319-20517-5_8openalex-snapshot
Photoperiodism: The Calendar of Plants
inferred← citeshttps://doi.org/10.1007/978-3-319-22521-0_6openalex-snapshot
Applying Epigenetics in Plant Breeding: Balancing Genome Stability and Phenotypic Plasticity
inferred← citeshttps://doi.org/10.1007/978-3-319-55520-1_20openalex-snapshot
Epigenetic Reprogramming During Plant Reproduction
inferred← citeshttps://doi.org/10.1007/978-981-10-8372-3_16openalex-snapshot
Theoretical and Applied Epigenetics in Plants
inferred← citeshttps://doi.org/10.1007/s00299-026-03747-3openalex-snapshot
Epigenetic regulation of floral transition: pathways and players
inferred← citeshttps://doi.org/10.1007/s00425-015-2451-9openalex-snapshot
The evolutionary landscape of PRC1 core components in green lineage
inferred← citeshttps://doi.org/10.1007/s00425-024-04479-yopenalex-snapshot
High expression of ethylene response factor BcERF98 delays the flowering time of non-heading Chinese cabbage
inferred← citeshttps://doi.org/10.1007/s11427-024-2784-3openalex-snapshot
Epigenetics in the modern era of crop improvements
inferred← citeshttps://doi.org/10.1007/s12374-024-09435-7openalex-snapshot
The Function of Like Heterochromatin Protein 1 (LHP1) as an Epigenetic Regulator of Plant Development
inferred← citeshttps://doi.org/10.1007/s42994-021-00065-yopenalex-snapshot
PRMT6 physically associates with nuclear factor Y to regulate photoperiodic flowering in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.celrep.2023.112738openalex-snapshot
TONSOKU is required for the maintenance of repressive chromatin modifications in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.devcel.2025.05.006openalex-snapshot
Calcium-responsive phosphorylation of SlLHP1b epigenetically suppresses auxin synthesis to control drought-induced flower drop in tomato
inferred← citeshttps://doi.org/10.1016/j.indcrop.2025.122424openalex-snapshot
Photoperiodic flowering in field crops: Mechanisms and the link to abiotic stresses
inferred← citeshttps://doi.org/10.1016/j.jcs.2019.05.008openalex-snapshot
QTL mapping for micronutrients concentration and yield component traits in a hexaploid wheat mapping population
inferred← citeshttps://doi.org/10.1016/j.jgg.2019.09.005openalex-snapshot
Histone modifications and their regulatory roles in plant development and environmental memory
inferred← citeshttps://doi.org/10.1016/j.molcel.2023.02.014openalex-snapshot
A pair of readers of bivalent chromatin mediate formation of Polycomb-based “memory of cold” in plants
inferred← citeshttps://doi.org/10.1016/j.molp.2015.08.005openalex-snapshot
The Arabidopsis RING Domain Protein BOI Inhibits Flowering via CO-dependent and CO-independent Mechanisms
inferred← citeshttps://doi.org/10.1016/j.molp.2018.01.010openalex-snapshot
Trithorax Group Proteins Act Together with a Polycomb Group Protein to Maintain Chromatin Integrity for Epigenetic Silencing during Seed Germination in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.molp.2018.06.007openalex-snapshot
Brassinosteroid Signaling Recruits Histone 3 Lysine-27 Demethylation Activity to FLOWERING LOCUS C Chromatin to Inhibit the Floral Transition in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.molp.2021.03.001openalex-snapshot
JASMONATE-ZIM DOMAIN proteins engage Polycomb chromatin modifiers to modulate Jasmonate signaling in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.molp.2021.04.010openalex-snapshot
Many ways to repress! JAZ’s agony of choices
inferred← citeshttps://doi.org/10.1016/j.pbi.2014.10.003openalex-snapshot
Polycomb repression in the regulation of growth and development in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.pbi.2015.11.010openalex-snapshot
The age of multiplexity: recruitment and interactions of Polycomb complexes in plants
inferred← citeshttps://doi.org/10.1016/j.pbi.2018.05.006openalex-snapshot
The seekers: how epigenetic modifying enzymes find their hidden genomic targets in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.pbi.2025.102783openalex-snapshot
Interplay between Polycomb-group associated histone modifiers and accessory proteins in plant evolution
inferred← citeshttps://doi.org/10.1016/j.plantsci.2023.111926openalex-snapshot
Epigenetic insight into floral transition and seed development in plants
inferred← citeshttps://doi.org/10.1016/j.plantsci.2024.112342openalex-snapshot
GmHSP40.1, a nuclear-localized soybean J domain protein, participates in regulation of flowering time through interacting with EMF1 and JMJ14
inferred← citeshttps://doi.org/10.1016/j.plantsci.2025.112740openalex-snapshot
Role of Like Heterochromatin Protein1 (LHP1) in the root apical meristem and stem cell niche maintenance in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.repbre.2022.11.003openalex-snapshot
Adaptation and integration of environmental cues to internal flowering network in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1016/j.scienta.2026.114818openalex-snapshot
Far-red-enriched ultra-long-day conditions induce constitutive FT expression and rapid flowering in radish rootstocks, promoting graft-mediated floral induction in Brassicaceae crops
inferred← citeshttps://doi.org/10.1016/j.semcdb.2020.05.007openalex-snapshot
Evolution and functional diversification of FLOWERING LOCUS T/TERMINAL FLOWER 1 family genes in plants
inferred← citeshttps://doi.org/10.1016/j.tig.2015.03.004openalex-snapshot
PcG and trxG in plants – friends or foes
inferred← citeshttps://doi.org/10.1016/j.tplants.2021.06.006openalex-snapshot
PRC2 activity, recruitment, and silencing: a comparative perspective
inferred← citeshttps://doi.org/10.1016/j.xplc.2019.100008openalex-snapshot
Genetic and Epigenetic Understanding of the Seasonal Timing of Flowering
inferred← citeshttps://doi.org/10.1016/j.xplc.2021.100267openalex-snapshot
Roles of Polycomb complexes in regulating gene expression and chromatin structure in plants
inferred← citeshttps://doi.org/10.1016/j.xplc.2025.101587openalex-snapshot
A histone deacetylase complex regulates anthocyanin biosynthesis during normal plant growth and development and in response to jasmonate
inferred← citeshttps://doi.org/10.1016/j.xplc.2026.101917openalex-snapshot
Antagonistic chromatin regulation of LHY homologs by GmASH2R and GmNF-YC4 fine-tunes soybean flowering time for latitudinal adaptation
inferred← citeshttps://doi.org/10.1021/bi500922qopenalex-snapshot
Circadian Clock and Photoperiodic Response in Arabidopsis : From Seasonal Flowering to Redox Homeostasis
inferred← citeshttps://doi.org/10.1038/celldisc.2015.3openalex-snapshot
C-terminal domains of histone demethylase JMJ14 interact with a pair of NAC transcription factors to mediate specific chromatin association
inferred← citeshttps://doi.org/10.1038/nature24300openalex-snapshot
Embryonic epigenetic reprogramming by a pioneer transcription factor in plants
inferred← citeshttps://doi.org/10.1038/ncomms15120openalex-snapshot
Temporal dynamics of gene expression and histone marks at the Arabidopsis shoot meristem during flowering
inferred← citeshttps://doi.org/10.1038/ng.3712openalex-snapshot
A cis cold memory element and a trans epigenome reader mediate Polycomb silencing of FLC by vernalization in Arabidopsis
inferred← citeshttps://doi.org/10.1038/nplants.2016.126openalex-snapshot
H2A deubiquitinases UBP12/13 are part of the Arabidopsis polycomb group protein system
inferred← citeshttps://doi.org/10.1038/nplants.2016.15openalex-snapshot
Coupling of histone methylation and RNA processing by the nuclear mRNA cap-binding complex
inferred← citeshttps://doi.org/10.1038/s41467-025-61328-6openalex-snapshot
Natural variation in histone demethylase GmLDL2 confers flowering time divergence for geographical expansion in soybean
inferred← citeshttps://doi.org/10.1038/s41467-025-64419-6openalex-snapshot
A pair of readers of histone H3K4 methylation recruit Polycomb repressive complex 2 to regulate photoperiodic flowering
inferred← citeshttps://doi.org/10.1038/s41477-018-0250-6openalex-snapshot
FRIGIDA establishes a local chromosomal environment for FLOWERING LOCUS C mRNA production
inferred← citeshttps://doi.org/10.1038/s41477-019-0402-3openalex-snapshot
Embryonic resetting of the parental vernalized state by two B3 domain transcription factors in Arabidopsis
inferred← citeshttps://doi.org/10.1038/s41477-020-00774-0openalex-snapshot
Maternal transmission of the epigenetic ‘memory of winter cold’ in Arabidopsis
inferred← citeshttps://doi.org/10.1038/s41477-023-01596-6openalex-snapshot
A molecular mechanism for embryonic resetting of winter memory and restoration of winter annual growth habit in wheat
inferred← citeshttps://doi.org/10.1038/s41477-025-02054-1openalex-snapshot
CK2 kinase–PRC2 signalling regulates genome-wide H3K27 trimethylation and transduces prolonged cold exposure into epigenetic cold memory in plants
inferred← citeshttps://doi.org/10.1038/s41477-026-02325-5openalex-snapshot
Resetting of epigenetic cold memory through somatic embryogenesis in plant regeneration
inferred← citeshttps://doi.org/10.1038/s41588-018-0190-0openalex-snapshot
Polycomb-mediated gene silencing by the BAH–EMF1 complex in plants
inferred← citeshttps://doi.org/10.1038/s42003-021-01907-7openalex-snapshot
GmBTB/POZ promotes the ubiquitination and degradation of LHP1 to regulate the response of soybean to Phytophthora sojae
inferred← citeshttps://doi.org/10.1042/bst20170576openalex-snapshot
Chromatin modulation and gene regulation in plants: insight about PRC1 function
inferred← citeshttps://doi.org/10.1042/bst20200192openalex-snapshot
Current understanding of plant Polycomb group proteins and the repressive histone H3 Lysine 27 trimethylation
inferred← citeshttps://doi.org/10.1073/pnas.2518761123openalex-snapshot
BpFLC coordinates seasonal and age-related flowering in Betula platyphylla through environmental cues and epigenetic regulation
inferred← citeshttps://doi.org/10.1073/pnas.2607481123openalex-snapshot
Dynamic Polycomb–CBC crosstalk orchestrates mRNA production at transcriptionally active loci in plants
inferred← citeshttps://doi.org/10.1080/19491034.2015.1038000openalex-snapshot
Enabling photoperiodic control of flowering by timely chromatin silencing of the florigen gene
inferred← citeshttps://doi.org/10.1093/aob/mcx082openalex-snapshot
Cell cycle arrest in plants: what distinguishes quiescence, dormancy and differentiated G1?
inferred← citeshttps://doi.org/10.1093/jxb/eraa216openalex-snapshot
Gene regulatory networks controlled by FLOWERING LOCUS C that confer variation in seasonal flowering and life history
inferred← citeshttps://doi.org/10.1093/jxb/erab248openalex-snapshot
Epigenetic regulation of temperature responses: past successes and future challenges
inferred← citeshttps://doi.org/10.1093/jxb/erae054openalex-snapshot
Epigenetics and plant hormone dynamics: a functional and methodological perspective
inferred← citeshttps://doi.org/10.1093/jxb/erag399openalex-snapshot
Oxygen sensing in plants: from dynamic hypoxia signalling to the expanding roles of the cysteine N-degron pathway
inferred← citeshttps://doi.org/10.1093/jxb/eru441openalex-snapshot
Time to flower: interplay between photoperiod and the circadian clock
inferred← citeshttps://doi.org/10.1093/pcp/pcae150openalex-snapshot
SHORT AND CROOKED AWN, encoding the epigenetic regulator EMF1, promotes barley awn development
inferred← citeshttps://doi.org/10.1093/pcp/pcw209openalex-snapshot
Governing the Silencing State of Chromatin: The Roles of Polycomb Repressive Complex 1 in Arabidopsis
inferred← citeshttps://doi.org/10.1093/plcell/koab139openalex-snapshot
EAR domain-containing transcription factors trigger PRC2-mediated chromatin marking in Arabidopsis
inferred← citeshttps://doi.org/10.1093/plcell/koac077openalex-snapshot
Embryonic reactivation of FLOWERING LOCUS C by ABSCISIC ACID-INSENSITIVE 3 establishes the vernalization requirement in each Arabidopsis generation
inferred← citeshttps://doi.org/10.1093/plcell/koad112openalex-snapshot
Binding by the Polycomb complex component BMI1 and H2A monoubiquitination shape local and long-range interactions in the Arabidopsis genome
inferred← citeshttps://doi.org/10.1093/plcell/koae287openalex-snapshot
EMBRYONIC FLOWER 1 regulates male reproduction by repressing the jasmonate pathway downstream transcription factor MYB26
inferred← citeshttps://doi.org/10.1093/plcell/koag101openalex-snapshot
LIKE HETEROCHROMATIN PROTEIN 1: a Polycomb-beyond composite regulator of chromatin in development, stress, and defense
inferred← citeshttps://doi.org/10.1093/plphys/kiab235openalex-snapshot
A microProtein repressor complex in the shoot meristem controls the transition to flowering
inferred← citeshttps://doi.org/10.1093/plphys/kiad292openalex-snapshot
PmAGAMOUS recruits polycomb protein PmLHP1 to regulate single-pistil morphogenesis in Japanese apricot
inferred← citeshttps://doi.org/10.1093/plphys/kiaf470openalex-snapshot
Targeted editing of H3K27me3 reveals its significance in the photoperiodic control of FLOWERING LOCUS T
inferred← citeshttps://doi.org/10.1101/2020.08.28.271999openalex-snapshot
Dissection of PRC1 and PRC2 recruitment in Arabidopsis connects EAR repressome to PRC2 anchoring
inferred← citeshttps://doi.org/10.1101/2023.08.07.552284openalex-snapshot
The two plant-specific DREAM components FLIC and FLAC repress floral transition in Arabidopsis
inferred← citeshttps://doi.org/10.1101/258228openalex-snapshot
Dissection of the microProtein miP1 floral repressor complex in Arabidopsis
inferred← citeshttps://doi.org/10.1101/gad.305227.117openalex-snapshot
Disruption of an RNA-binding hinge region abolishes LHP1-mediated epigenetic repression
inferred← citeshttps://doi.org/10.1104/pp.15.00073openalex-snapshot
Deciphering the Role of POLYCOMB REPRESSIVE COMPLEX1 Variants in Regulating the Acquisition of Flowering Competence in Arabidopsis
inferred← citeshttps://doi.org/10.1104/pp.15.00496openalex-snapshot
Flowering Locus C’s Lessons: Conserved Chromatin Switches Underpinning Developmental Timing and Adaptation
inferred← citeshttps://doi.org/10.1104/pp.15.00535openalex-snapshot
Florigen-Encoding Genes of Day-Neutral and Photoperiod-Sensitive Maize Are Regulated by Different Chromatin Modifications at the Floral Transition
inferred← citeshttps://doi.org/10.1104/pp.16.00193openalex-snapshot
ZRF1 Chromatin Regulators Have Polycomb Silencing and Independent Roles in Development
inferred← citeshttps://doi.org/10.1104/pp.16.01259openalex-snapshot
The Arabidopsis Polycomb Repressive Complex 1 (PRC1) Components AtBMI1A, B, and C Impact Gene Networks throughout All Stages of Plant Development
inferred← citeshttps://doi.org/10.1104/pp.18.00296openalex-snapshot
Temporal-Specific Interaction of NF-YC and CURLY LEAF during the Floral Transition Regulates Flowering
inferred← citeshttps://doi.org/10.1104/pp.19.00596openalex-snapshot
The Chromatin-Remodeling Factor PICKLE Antagonizes Polycomb Repression of FT to Promote Flowering
inferred← citeshttps://doi.org/10.1104/pp.19.00642openalex-snapshot
The B3-Domain Transcription Factor VAL1 Regulates the Floral Transition by Repressing FLOWERING LOCUS T
inferred← citeshttps://doi.org/10.1104/pp.19.00793openalex-snapshot
HISTONE DEACETYLASE 9 Functions with Polycomb Silencing to Repress FLOWERING LOCUS C Expression
inferred← citeshttps://doi.org/10.1104/pp.20.00056openalex-snapshot
AGAMOUS-LIKE67 Cooperates with the Histone Mark Reader EBS to Modulate Seed Germination under High Temperature
inferred← citeshttps://doi.org/10.1105/tpc.17.00714openalex-snapshot
Phloem Companion Cell-Specific Transcriptomic and Epigenomic Analyses Identify MRF1, a Regulator of Flowering
inferred← citeshttps://doi.org/10.1111/nph.13486openalex-snapshot
The impact of Polycomb group (PcG) and Trithorax group (TrxG) epigenetic factors in plant plasticity
inferred← citeshttps://doi.org/10.1111/nph.16602openalex-snapshot
Transcriptional regulatory network of the light signaling pathways
inferred← citeshttps://doi.org/10.1111/nph.16616openalex-snapshot
MRG1/2 histone methylation readers and HD2C histone deacetylase associate in repression of the florigen gene FT to set a proper flowering time in response to day‐length changes
inferred← citeshttps://doi.org/10.1111/pbi.70097openalex-snapshot
CmFDa ‐mediated epigenetic regulation of flowering in chrysanthemum
inferred← citeshttps://doi.org/10.1111/pbr.13148openalex-snapshot
Epigenetic‐based control of flowering and seed development in plants: A review
inferred← citeshttps://doi.org/10.1111/pce.13557openalex-snapshot
The chromatin‐remodelling factor PICKLE interacts with CONSTANS to promote flowering in Arabidopsis
inferred← citeshttps://doi.org/10.1111/pce.15469openalex-snapshot
A J‐Domain Protein J3 Antagonizes ABI5‐BINDING PROTEIN2 to Regulate CONSTANS Stability and Flowering Time
inferred← citeshttps://doi.org/10.1111/pce.70749openalex-snapshot
The FT/TFL1 Regulatory Module: A Synthesis of Gene Duplication, Functional Divergence, and Environmental Modulation Across Plant Lineages
inferred← citeshttps://doi.org/10.1111/ppl.13163openalex-snapshot
The molecular mechanism of vernalization in Arabidopsis and cereals: role of Flowering Locus C and its homologs
inferred← citeshttps://doi.org/10.1111/tpj.12818openalex-snapshot
PRC 1 is taking the lead in P c G repression
inferred← citeshttps://doi.org/10.1111/tpj.12828openalex-snapshot
Keeping the gate closed: functions of the polycomb repressive complex PRC 2 in development
inferred← citeshttps://doi.org/10.1111/tpj.13926openalex-snapshot
The NUCLEAR FACTOR ‐ CONSTANS complex antagonizes Polycomb repression to de‐repress FLOWERING LOCUS T expression in response to inductive long days in Arabidopsis
inferred← citeshttps://doi.org/10.1111/tpj.14182openalex-snapshot
Functional characterization of LIKE HETEROCHROMATIN PROTEIN 1 in the moss Physcomitrella patens: its conserved protein interactions in land plants
inferred← citeshttps://doi.org/10.1111/tpj.14430openalex-snapshot
SIN3 LIKE genes mediate long‐day induction of flowering but inhibit the floral transition in short days through histone deacetylation in Arabidopsis
inferred← citeshttps://doi.org/10.1111/tpj.14796openalex-snapshot
Nuclear import of LIKE HETEROCHROMATIN PROTEIN1 is redundantly mediated by importins α‐1, α‐2 and α‐3
inferred← citeshttps://doi.org/10.1111/tpj.70815openalex-snapshot
Ethylene signaling promotes seed‐derived somatic embryogenesis by directly activating LEAFY COTYLEDON 1 in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1126/science.adf8822openalex-snapshot
Control of histone demethylation by nuclear-localized α-ketoglutarate dehydrogenase
inferred← citeshttps://doi.org/10.1134/s102279542011006xopenalex-snapshot
The Evolutionary Aspects of Flowering Control: Florigens and Anti-Florigens
inferred← citeshttps://doi.org/10.1146/annurev-arplant-043014-115627openalex-snapshot
The Polycomb Group Protein Regulatory Network
inferred← citeshttps://doi.org/10.1146/annurev-cellbio-100616-060546openalex-snapshot
The FLC Locus: A Platform for Discoveries in Epigenetics and Adaptation
inferred← citeshttps://doi.org/10.1186/s12864-019-5905-9openalex-snapshot
Evolution and conservation of polycomb repressive complex 1 core components and putative associated factors in the green lineage
inferred← citeshttps://doi.org/10.1186/s12870-024-04866-3openalex-snapshot
Identification of epigenetically regulated genes involved in plant-virus interaction and their role in virus-triggered induced resistance
inferred← citeshttps://doi.org/10.1186/s13059-015-0770-6openalex-snapshot
Molecular memories in the regulation of seasonal flowering: from competence to cessation
inferred← citeshttps://doi.org/10.1186/s13059-017-1197-zopenalex-snapshot
H2A monoubiquitination in Arabidopsis thaliana is generally independent of LHP1 and PRC2 activity
inferred← citeshttps://doi.org/10.1186/s13059-026-04217-5openalex-snapshot
ZmEMF1a is required for the maintenance of H2Aub and H3K27me3 modifications in maize kernel development
inferred← citeshttps://doi.org/10.12688/f1000research.21180.1openalex-snapshot
LEAFY COTYLEDONs: old genes with new roles beyond seed development
inferred← citeshttps://doi.org/10.1371/journal.pgen.1004975openalex-snapshot
The Arabidopsis DNA Polymerase δ Has a Role in the Deposition of Transcriptionally Active Epigenetic Marks, Development and Flowering
inferred← citeshttps://doi.org/10.1371/journal.pgen.1005660openalex-snapshot
Kicking against the PRCs – A Domesticated Transposase Antagonises Silencing Mediated by Polycomb Group Proteins and Is an Accessory Component of Polycomb Repressive Complex 2
inferred← citeshttps://doi.org/10.1371/journal.pgen.1005771openalex-snapshot
Arabidopsis Flower and Embryo Developmental Genes are Repressed in Seedlings by Different Combinations of Polycomb Group Proteins in Association with Distinct Sets of Cis-regulatory Elements
inferred← citeshttps://doi.org/10.1371/journal.pgen.1008065openalex-snapshot
Floral regulators FLC and SOC1 directly regulate expression of the B3-type transcription factor TARGET OF FLC AND SVP 1 at the Arabidopsis shoot apex via antagonistic chromatin modifications
inferred← citeshttps://doi.org/10.1371/journal.pgen.1008377openalex-snapshot
BZU2/ZmMUTE controls symmetrical division of guard mother cell and specifies neighbor cell fate in maize
inferred← citeshttps://doi.org/10.1371/journal.pgen.1008681openalex-snapshot
The domesticated transposase ALP2 mediates formation of a novel Polycomb protein complex by direct interaction with MSI1, a core subunit of Polycomb Repressive Complex 2 (PRC2)
inferred← citeshttps://doi.org/10.1371/journal.pone.0158936openalex-snapshot
LHP1 Regulates H3K27me3 Spreading and Shapes the Three-Dimensional Conformation of the Arabidopsis Genome
inferred← citeshttps://doi.org/10.21203/rs.3.rs-3138103/v1openalex-snapshot
Identification of epigenetically regulated genes involved in plant-virus interaction and their role in virus-triggered induced resistance
inferred← citeshttps://doi.org/10.3389/fpls.2017.00867openalex-snapshot
Polycomb Group Proteins RING1A and RING1B Regulate the Vegetative Phase Transition in Arabidopsis
inferred← citeshttps://doi.org/10.3389/fpls.2017.02041openalex-snapshot
LHP1 Could Act as an Activator and a Repressor of Transcription in Plants
inferred← citeshttps://doi.org/10.3389/fpls.2021.637244openalex-snapshot
The Epigenetic Faces of ULTRAPETALA1
inferred← citeshttps://doi.org/10.3389/fpls.2022.967607openalex-snapshot
Methylation hallmarks on the histone tail as a linker of osmotic stress and gene transcription
inferred← citeshttps://doi.org/10.3389/fpls.2026.1829334openalex-snapshot
QTL mapping of vernalization-insensitive and photoperiod-independent early flowering in yellow lupin (Lupinus luteus L.)
inferred← citeshttps://doi.org/10.3390/books978-3-0365-5023-7openalex-snapshot
Advances in the Molecular Mechanisms of Abscisic Acid and Gibberellins Functions in Plants 2.0
inferred← citeshttps://doi.org/10.3390/horticulturae9020199openalex-snapshot
The Potential Use of the Epigenetic Remodeler LIKE HETEROCHROMATIN PROTEIN 1 (LHP1) as a Tool for Crop Improvement
inferred← citeshttps://doi.org/10.3390/ijms21030872openalex-snapshot
Roles of Brassinosteroids in Plant Reproduction
inferred← citeshttps://doi.org/10.3390/ijms21165871openalex-snapshot
Knowing When to Silence: Roles of Polycomb-Group Proteins in SAM Maintenance, Root Development, and Developmental Phase Transition
inferred← citeshttps://doi.org/10.3390/ijms21249700openalex-snapshot
Abscisic Acid and Flowering Regulation: Many Targets, Different Places
inferred← citeshttps://doi.org/10.3390/ijms22147559openalex-snapshot
QTL Mapping and Diurnal Transcriptome Analysis Identify Candidate Genes Regulating Brassica napus Flowering Time
inferred← citeshttps://doi.org/10.3390/ijms23010466openalex-snapshot
Molecular Genetic Understanding of Photoperiodic Regulation of Flowering Time in Arabidopsis and Soybean
inferred← citeshttps://doi.org/10.3390/ijms242417248openalex-snapshot
Arabidopsis SEC13B Interacts with Suppressor of Frigida 4 to Repress Flowering
inferred← citeshttps://doi.org/10.3390/plants11192635openalex-snapshot
Mapping of Two Major QTLs Controlling Flowering Time in Brassica napus Using a High-Density Genetic Map
inferred← citeshttps://doi.org/10.3390/plants12183299openalex-snapshot
Beyond NPK: Mineral Nutrient-Mediated Modulation in Orchestrating Flowering Time
inferred← citeshttps://doi.org/10.3410/f.726955986.793568953openalex-snapshot
Faculty Opinions recommendation of The Arabidopsis Polycomb Repressive Complex 1 (PRC1) Components AtBMI1A, B, and C Impact Gene Networks throughout All Stages of Plant Development.
inferred← citeshttps://doi.org/10.3410/f.740134649.793586332openalex-snapshot
Faculty Opinions recommendation of EAR domain-containing transcription factors trigger PRC2-mediated chromatin marking in Arabidopsis.
inferred← citeshttps://doi.org/10.48130/seedbio-0026-0007openalex-snapshot
Beyond flowering: the pleiotropic functions of key flowering-time genes
inferred← citeshttps://doi.org/10.6084/m9.figshare.25347176openalex-snapshot
Additional file 1 of Identification of epigenetically regulated genes involved in plant-virus interaction and their role in virus-triggered induced resistance
inferred← citeshttps://doi.org/10.6084/m9.figshare.25347205openalex-snapshot
Additional file 2 of Identification of epigenetically regulated genes involved in plant-virus interaction and their role in virus-triggered induced resistance
inferred← citeshttps://doi.org/10.6084/m9.figshare.26688971openalex-snapshot
Additional file 3 of Identification of epigenetically regulated genes involved in plant-virus interaction and their role in virus-triggered induced resistance
inferred← citeshttps://doi.org/10.6084/m9.figshare.26688974openalex-snapshot
Additional file 4 of Identification of epigenetically regulated genes involved in plant-virus interaction and their role in virus-triggered induced resistance
inferred← citeshttps://doi.org/10.6084/m9.figshare.26688977openalex-snapshot
Additional file 5 of Identification of epigenetically regulated genes involved in plant-virus interaction and their role in virus-triggered induced resistance
inferred← citeshttps://doi.org/10.6084/m9.figshare.26688980openalex-snapshot
Additional file 6 of Identification of epigenetically regulated genes involved in plant-virus interaction and their role in virus-triggered induced resistance
inferred← citeshttps://doi.org/10.6084/m9.figshare.26688983openalex-snapshot
Additional file 7 of Identification of epigenetically regulated genes involved in plant-virus interaction and their role in virus-triggered induced resistance
inferred← citeshttps://doi.org/10.6084/m9.figshare.26688986openalex-snapshot
Additional file 8 of Identification of epigenetically regulated genes involved in plant-virus interaction and their role in virus-triggered induced resistance
inferred← citeshttps://doi.org/10.6084/m9.figshare.26688989openalex-snapshot
Additional file 9 of Identification of epigenetically regulated genes involved in plant-virus interaction and their role in virus-triggered induced resistance
inferred← citeshttps://doi.org/10.6084/m9.figshare.26688992openalex-snapshot
Additional file 10 of Identification of epigenetically regulated genes involved in plant-virus interaction and their role in virus-triggered induced resistance
inferred← citeshttps://doi.org/10.6084/m9.figshare.26688995openalex-snapshot
Additional file 11 of Identification of epigenetically regulated genes involved in plant-virus interaction and their role in virus-triggered induced resistance
inferred← citeshttps://doi.org/10.6084/m9.figshare.26688998openalex-snapshot
Additional file 12 of Identification of epigenetically regulated genes involved in plant-virus interaction and their role in virus-triggered induced resistance
inferred← citeshttps://doi.org/10.70675/c4d7f7a2z4e27z4e37z958ez5814de53d94fopenalex-snapshot
Depicting some chromatin-based mechanisms behind Arabidopsis thaliana stress responses
inferred← citeshttps://doi.org/10.70675/e4d5eceaz8544z4d02zb4d4zd09e40e13936openalex-snapshot
Role of chromatin regulators AtRING1 and AtZRF1 in Arabidopsis growth and development
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