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PIN2-like proteins may contribute to the regulation of morphogenetic processes during spermatogenesis in Chara vulgaris

https://doi.org/10.1007/s00299-016-1979-x
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What this work says

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

inferredcites →https://doi.org/10.1007/978-3-642-40288-3openalex-snapshot
The Physiology of Characean Cells
inferredcites →https://doi.org/10.1007/978-3-642-60035-7_12openalex-snapshot
Plasmodesmal Cou lin p g and Cell Differentiation in Aigae
inferredcites →https://doi.org/10.1007/bf00392816openalex-snapshot
Reorganization of the endoplasmic reticulum in epidermal cells of onion bulb scales after cold stress: Involvement of cytoskeletal elements
inferredcites →https://doi.org/10.1007/bf00397384openalex-snapshot
Changes in ultrastructure of plasmodesmata during spermatogenesis in Chara vulgaris L.
inferredcites →https://doi.org/10.1007/bf00937825openalex-snapshot
Endopolyploidization patterns in non-generative antheridial cells in mono- and dioeciousChara spp. (Characeae) with different DNA C-values
inferredcites →https://doi.org/10.1007/bf00942143openalex-snapshot
Cell cycle duration in antheridial filaments ofChara spp. (Characeae) with different genome size and heterochromatin content
inferredcites →https://doi.org/10.1007/bf01276998openalex-snapshot
Changes in the occurrence and ultrastructure of plasmodesmata in antheridia ofChara vulgaris L. during different stages of spermatogenesis
inferredcites →https://doi.org/10.1007/bf01290870openalex-snapshot
Symplasmic isolation ofChara vulgaris antheridium and mechanisms regulating the process of spermatogenesis
inferredcites →https://doi.org/10.1007/bf01322627openalex-snapshot
Biological role of endoreplication in the process of spermatogenesis inChara vulgaris L.
inferredcites →https://doi.org/10.1007/bf01624003openalex-snapshot
Plasmodesmata between synchronously and asynchronously developing cells of the antheridial filaments ofChara vulgaris L.
inferredcites →https://doi.org/10.1007/s00709-003-0001-yopenalex-snapshot
Plasmodesmal changes are related to different developmental stages of antheridia of Chara species
inferredcites →https://doi.org/10.1016/j.cell.2007.07.033openalex-snapshot
Antagonistic Regulation of PIN Phosphorylation by PP2A and PINOID Directs Auxin Flux
inferredcites →https://doi.org/10.1016/j.cell.2009.03.001openalex-snapshot
Auxin: A Trigger for Change in Plant Development
inferredcites →https://doi.org/10.1016/j.cub.2014.09.054openalex-snapshot
Plasma Membrane-Targeted PIN Proteins Drive Shoot Development in a Moss
inferredcites →https://doi.org/10.1016/j.cub.2014.09.056openalex-snapshot
Directional Auxin Transport Mechanisms in Early Diverging Land Plants
inferredcites →https://doi.org/10.1016/j.devcel.2013.12.008openalex-snapshot
Auxin-Callose-Mediated Plasmodesmal Gating Is Essential for Tropic Auxin Gradient Formation and Signaling
inferredcites →https://doi.org/10.1016/j.jplph.2014.09.013openalex-snapshot
The biphasic interphase-mitotic polarity of cell nuclei induced under DNA replication stress seems to be correlated with Pin2 localization in root meristems of Allium cepa
inferredcites →https://doi.org/10.1016/j.phytochem.2014.11.008openalex-snapshot
Interplays between the cell wall and phytohormones in interaction between plants and necrotrophic pathogens
inferredcites →https://doi.org/10.1016/j.tplants.2009.01.004openalex-snapshot
Auxin signaling in algal lineages: fact or myth?
inferredcites →https://doi.org/10.1016/j.tplants.2015.05.005openalex-snapshot
PIN proteins and the evolution of plant development
inferredcites →https://doi.org/10.1016/s0015-3796(80)80072-2openalex-snapshot
Auxin as a factor regulating initiation, of mitosis in antheridial filaments of Chara vulgaris L.
inferredcites →https://doi.org/10.1016/s0091-679x(08)60191-0openalex-snapshot
Chapter 8 Fluorescent Labeling of Endoplasmic Reticulum
inferredcites →https://doi.org/10.1023/a:1015242627321openalex-snapshot
Evolutionary patterns in auxin action
inferredcites →https://doi.org/10.1023/b:rudo.0000007890.08452.c4openalex-snapshot
Role of Auxin in Induction of Polarity in Fucus vesiculosus Zygotes
inferredcites →https://doi.org/10.1071/bi9670539openalex-snapshot
Ultrastructure and Differentiation in Chara Sp.I. Vegetative Cells
inferredcites →https://doi.org/10.1071/bi9680255openalex-snapshot
Ultrastructure and Differentiation In Chara Sp. III. Formation of the Antheridium
inferredcites →https://doi.org/10.1080/07352689.2011.615705openalex-snapshot
Phylogeny and Molecular Evolution of the Green Algae
inferredcites →https://doi.org/10.1093/aob/mcn266openalex-snapshot
Ectopic expression of LEAFY COTYLEDON1-LIKE gene and localized auxin accumulation mark embryogenic competence in epiphyllous plants of Helianthus annuus × H. tuberosus
inferredcites →https://doi.org/10.1093/aob/mcp193openalex-snapshot
The distribution of cell wall polymers during antheridium development and spermatogenesis in the Charophycean green alga, Chara corallina
inferredcites →https://doi.org/10.1093/emboj/17.23.6903openalex-snapshot
AtPIN2 defines a locus of Arabidopsis for root gravitropism control
inferredcites →https://doi.org/10.1093/jxb/ers106openalex-snapshot
Polar auxin transport: an early invention
inferredcites →https://doi.org/10.1093/jxb/ert322openalex-snapshot
Molecular and biochemical analysis of the first ARA6 homologue, a RAB5 GTPase, from green algae
inferredcites →https://doi.org/10.1093/pcp/pcj067openalex-snapshot
Cortical Microtubule Arrays Lose Uniform Alignment Between Cells and are Oryzalin Resistant in the Arabidopsis Mutant, radially swollen 6
inferredcites →https://doi.org/10.1101/cshperspect.a001537openalex-snapshot
Auxin Control of Root Development
inferredcites →https://doi.org/10.1101/cshperspect.a001552openalex-snapshot
Auxin Transporters--Why So Many?
inferredcites →https://doi.org/10.1104/pp.004747openalex-snapshot
Early Embryo Development in Fucus distichus Is Auxin Sensitive
inferredcites →https://doi.org/10.1104/pp.108.121756openalex-snapshot
PIN Polar Targeting
inferredcites →https://doi.org/10.1104/pp.109.149708openalex-snapshot
Auxin Metabolism and Function in the Multicellular Brown Alga Ectocarpus siliculosus
inferredcites →https://doi.org/10.1105/tpc.013169openalex-snapshot
The Mitochondrial Genome of Chara vulgaris: Insights into the Mitochondrial DNA Architecture of the Last Common Ancestor of Green Algae and Land Plants[W]
inferredcites →https://doi.org/10.1105/tpc.108.060418openalex-snapshot
The Evolving Complexity of the Auxin Pathway
inferredcites →https://doi.org/10.1105/tpc.110.075317openalex-snapshot
Gravitropism ofArabidopsis thalianaRoots Requires the Polarization of PIN2 toward the Root Tip in Meristematic Cortical Cells
inferredcites →https://doi.org/10.1105/tpc.113.114868openalex-snapshot
A Kinetic Analysis of the Auxin Transcriptome Reveals Cell Wall Remodeling Proteins That Modulate Lateral Root Development in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1365-313x.2006.02986.xopenalex-snapshot
A plasmodesmata‐associated β ‐1,3‐glucanase in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1438-8677.1996.tb00550.xopenalex-snapshot
Different Patterns of Intercellular Transport of Lucifer Yellow in Young and Mature Antheridia of Chara vulgaris L.
inferredcites →https://doi.org/10.1111/j.1469-8137.1993.tb03897.xopenalex-snapshot
Plasmodesmata and the supracellular nature of plants
inferredcites →https://doi.org/10.1111/j.1469-8137.2005.01466.xopenalex-snapshot
Evolution of leaf developmental mechanisms
inferredcites →https://doi.org/10.1111/j.1525-142x.2008.00225.xopenalex-snapshot
Convergent evolution of shoots in land plants: lack of auxin polar transport in moss shoots
inferredcites →https://doi.org/10.1126/science.1065156openalex-snapshot
The Closest Living Relatives of Land Plants
inferredcites →https://doi.org/10.1126/science.1100618openalex-snapshot
A PINOID-Dependent Binary Switch in Apical-Basal PIN Polar Targeting Directs Auxin Efflux
inferredcites →https://doi.org/10.1146/annurev-arplant-042809-112308openalex-snapshot
Auxin Biosynthesis and Its Role in Plant Development
inferredcites →https://doi.org/10.1146/annurev.arplant.58.032806.103805openalex-snapshot
Auxin: The Looping Star in Plant Development
inferredcites →https://doi.org/10.1186/gb-2009-10-12-249openalex-snapshot
The PIN-FORMED (PIN) protein family of auxin transporters
inferredcites →https://doi.org/10.1242/dev.052456openalex-snapshot
Plasma membrane-bound AGC3 kinases phosphorylate PIN auxin carriers at TPRXS(N/S) motifs to direct apical PIN recycling
inferredcites →https://doi.org/10.1371/journal.pbio.0060307openalex-snapshot
Root System Architecture from Coupling Cell Shape to Auxin Transport
inferredcites →https://doi.org/10.1371/journal.pone.0057813openalex-snapshot
Mechano-Chemical Aspects of Organ Formation in Arabidopsis thaliana: The Relationship between Auxin and Pectin
inferredcites →https://doi.org/10.3389/fpls.2012.00225openalex-snapshot
AUX/LAX family of auxin influx carriers—an overview
inferredcites →https://doi.org/10.3389/fpls.2014.00074openalex-snapshot
Plasmodesmata without callose and calreticulin in higher plants – open channels for fast symplastic transport?
inferredcites →https://doi.org/10.3724/sp.j.1002.2008.08035openalex-snapshot
Phylogeny and evolution of charophytic algae and land plants
inferredcites →https://doi.org/10.4161/psb.4.6.8359openalex-snapshot
Callose synthesis in higher plants
inferredcites →https://doi.org/10.5586/asbp.1929.014openalex-snapshot
Garnitures des chromosomes et synchronisme des divisions dans lesfilaments d'anthérozoïdes chez certaines espèces du genre Chara Vaill.
inferredcites →https://doi.org/10.5586/asbp.1988.003openalex-snapshot
Callose formation in injured cells of the vegetative and generative thallus of Chara vulgaris L. Absence of callose in the process of cytodifferentiation

What points at this work

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

inferred← citeshttps://doi.org/10.3897/oneeco.9.e117655zenodo-depositor-declared
What we really know about the dormancy, reproduction, germination and cultivation of charophytes (Characeae)
inferred← citeshttps://doi.org/10.1007/s00299-020-02545-9openalex-snapshot
5-Aminouracil and other inhibitors of DNA replication induce biphasic interphase–mitotic cells in apical root meristems of Allium cepa
inferred← citeshttps://doi.org/10.1007/s00709-023-01900-3openalex-snapshot
Rediscovering Chara as a model organism for molecular and evo-devo studies
inferred← citeshttps://doi.org/10.1007/s10265-023-01494-0openalex-snapshot
Plasmodesmata callose binding protein 2 contributes to the regulation of cambium/phloem formation and auxin response during the tissue reunion process in incised Arabidopsis stem
inferred← citeshttps://doi.org/10.1016/j.cell.2020.04.019openalex-snapshot
The Penium margaritaceum Genome: Hallmarks of the Origins of Land Plants
inferred← citeshttps://doi.org/10.1016/j.pbi.2018.02.004openalex-snapshot
What have we learnt from studying the evolution of the arbuscular mycorrhizal symbiosis?
inferred← citeshttps://doi.org/10.1016/j.semcdb.2022.03.004openalex-snapshot
Crossroads in the evolution of plant specialized metabolism
inferred← citeshttps://doi.org/10.1016/j.xplc.2026.101892openalex-snapshot
Evolutionary shifts in plant adaptation mediated by phytohormones
inferred← citeshttps://doi.org/10.1038/s41477-019-0542-5openalex-snapshot
PIN-driven auxin transport emerged early in streptophyte evolution
inferred← citeshttps://doi.org/10.1038/s41588-024-01737-3openalex-snapshot
Genomes of multicellular algal sisters to land plants illuminate signaling network evolution
inferred← citeshttps://doi.org/10.1073/pnas.2412493121openalex-snapshot
Origin and evolution of auxin-mediated acid growth
inferred← citeshttps://doi.org/10.1093/jxb/eraa007openalex-snapshot
Evo-physio: on stress responses and the earliest land plants
inferred← citeshttps://doi.org/10.1093/jxb/eraa169openalex-snapshot
The evolutionary origins of auxin transport: what we know and what we need to know
inferred← citeshttps://doi.org/10.1093/plphys/kiag439openalex-snapshot
Evolutionary and structural analysis reveals the gradual establishment and high conservation of auxin pathways from algae to land plants
inferred← citeshttps://doi.org/10.1101/2024.10.16.618682openalex-snapshot
The role of IAA and its transport in the complex streptophyte algae Chara braunii
inferred← citeshttps://doi.org/10.1104/pp.17.00274openalex-snapshot
Primitive Auxin Response without TIR1 and Aux/IAA in the Charophyte Alga Klebsormidium nitens
inferred← citeshttps://doi.org/10.1111/nph.18691openalex-snapshot
A Physcomitrella PIN protein acts in spermatogenesis and sporophyte retention
inferred← citeshttps://doi.org/10.1111/nph.70019openalex-snapshot
The role of indole‐3‐acetic acid and characterization of PIN transporters in complex streptophyte alga Chara braunii
inferred← citeshttps://doi.org/10.1126/sciadv.abc8895openalex-snapshot
Functional innovations of PIN auxin transporters mark crucial evolutionary transitions during rise of flowering plants
inferred← citeshttps://doi.org/10.1146/annurev-arplant-083123-060254openalex-snapshot
Systems Biology of Streptophyte Cell Evolution
inferred← citeshttps://doi.org/10.1186/s12870-021-03117-zopenalex-snapshot
Differential gene expression patterns during gametophyte development provide insights into sex differentiation in the dioicous kelp Saccharina japonica
inferred← citeshttps://doi.org/10.3389/fpls.2016.00866openalex-snapshot
Enzyme-Less Growth in Chara and Terrestrial Plants
inferred← citeshttps://doi.org/10.3390/cells9030606openalex-snapshot
The Winner Takes It All: Auxin—The Main Player during Plant Embryogenesis
inferred← citeshttps://doi.org/10.3390/plants9111527openalex-snapshot
ER-Localized PIN Carriers: Regulators of Intracellular Auxin Homeostasis
inferred← citeshttps://doi.org/10.6084/m9.figshare.14984810openalex-snapshot
Additional file 10 of Differential gene expression patterns during gametophyte development provide insights into sex differentiation in the dioicous kelp Saccharina japonica
inferred← citeshttps://doi.org/10.6084/m9.figshare.14984813openalex-snapshot
Additional file 11 of Differential gene expression patterns during gametophyte development provide insights into sex differentiation in the dioicous kelp Saccharina japonica
inferred← citeshttps://doi.org/10.6084/m9.figshare.14984816openalex-snapshot
Additional file 12 of Differential gene expression patterns during gametophyte development provide insights into sex differentiation in the dioicous kelp Saccharina japonica
inferred← citeshttps://doi.org/10.6084/m9.figshare.14984819openalex-snapshot
Additional file 13 of Differential gene expression patterns during gametophyte development provide insights into sex differentiation in the dioicous kelp Saccharina japonica
inferred← citeshttps://doi.org/10.6084/m9.figshare.14984822openalex-snapshot
Additional file 14 of Differential gene expression patterns during gametophyte development provide insights into sex differentiation in the dioicous kelp Saccharina japonica
inferred← citeshttps://doi.org/10.6084/m9.figshare.14984825openalex-snapshot
Additional file 15 of Differential gene expression patterns during gametophyte development provide insights into sex differentiation in the dioicous kelp Saccharina japonica
inferred← citeshttps://doi.org/10.6084/m9.figshare.14984828openalex-snapshot
Additional file 16 of Differential gene expression patterns during gametophyte development provide insights into sex differentiation in the dioicous kelp Saccharina japonica
inferred← citeshttps://doi.org/10.6084/m9.figshare.14984831openalex-snapshot
Additional file 17 of Differential gene expression patterns during gametophyte development provide insights into sex differentiation in the dioicous kelp Saccharina japonica
inferred← citeshttps://doi.org/10.6084/m9.figshare.14984834openalex-snapshot
Additional file 1 of Differential gene expression patterns during gametophyte development provide insights into sex differentiation in the dioicous kelp Saccharina japonica
inferred← citeshttps://doi.org/10.6084/m9.figshare.14984837openalex-snapshot
Additional file 2 of Differential gene expression patterns during gametophyte development provide insights into sex differentiation in the dioicous kelp Saccharina japonica
inferred← citeshttps://doi.org/10.6084/m9.figshare.14984840openalex-snapshot
Additional file 3 of Differential gene expression patterns during gametophyte development provide insights into sex differentiation in the dioicous kelp Saccharina japonica
inferred← citeshttps://doi.org/10.6084/m9.figshare.14984843openalex-snapshot
Additional file 4 of Differential gene expression patterns during gametophyte development provide insights into sex differentiation in the dioicous kelp Saccharina japonica
inferred← citeshttps://doi.org/10.6084/m9.figshare.14984846openalex-snapshot
Additional file 5 of Differential gene expression patterns during gametophyte development provide insights into sex differentiation in the dioicous kelp Saccharina japonica
inferred← citeshttps://doi.org/10.6084/m9.figshare.14984849openalex-snapshot
Additional file 6 of Differential gene expression patterns during gametophyte development provide insights into sex differentiation in the dioicous kelp Saccharina japonica
inferred← citeshttps://doi.org/10.6084/m9.figshare.14984852openalex-snapshot
Additional file 7 of Differential gene expression patterns during gametophyte development provide insights into sex differentiation in the dioicous kelp Saccharina japonica
inferred← citeshttps://doi.org/10.6084/m9.figshare.14984855openalex-snapshot
Additional file 8 of Differential gene expression patterns during gametophyte development provide insights into sex differentiation in the dioicous kelp Saccharina japonica
inferred← citeshttps://doi.org/10.6084/m9.figshare.14984858openalex-snapshot
Additional file 9 of Differential gene expression patterns during gametophyte development provide insights into sex differentiation in the dioicous kelp Saccharina japonica
inferred← citeshttps://doi.org/10.70675/dd88298cz5befz4ffbzad13za2b67ce345d7openalex-snapshot
Characterization of the evolution of the molecular mechanisms governing arbuscular mycorrhizal symbiosis in land plants
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