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Dynamic morphologies of pollen plastids visualised by vegetative-specific FtsZ1–GFP in Arabidopsis thaliana

https://doi.org/10.1007/s00709-010-0119-7
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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/cm.10168openalex-snapshot
A subclass of myosin XI is associated with mitochondria, plastids, and the molecular chaperone subunit TCP‐1α in maize
inferredcites →https://doi.org/10.1002/cm.20181openalex-snapshot
Differential organelle movement on the actin cytoskeleton in lily pollen tubes
inferredcites →https://doi.org/10.1007/978-1-4020-3166-3openalex-snapshot
Molecular Biology and Biotechnology of Plant Organelles
inferredcites →https://doi.org/10.1007/978-1-4020-3166-3_4openalex-snapshot
The Sexual Inheritance of Plant Organelles
inferredcites →https://doi.org/10.1007/bf00205228openalex-snapshot
Dynamic aspects of apical zonation in the angiosperm pollen tube
inferredcites →https://doi.org/10.1007/bf00230513openalex-snapshot
Anther starch variations in Lilium during pollen development
inferredcites →https://doi.org/10.1007/bf01273170openalex-snapshot
Dynamics of vegetative cytoplasm during generative cell formation and pollen maturation inArabidopsis thaliana
inferredcites →https://doi.org/10.1007/bf02441957openalex-snapshot
Types and meaning of pollen carbohydrate reserves
inferredcites →https://doi.org/10.1007/bf02524262openalex-snapshot
Isolation of theftsZ gene from plastid-deficient generative cells ofLilium longiflorum
inferredcites →https://doi.org/10.1007/s00239-003-2551-1openalex-snapshot
Two Types of FtsZ Proteins in Mitochondria and Red-Lineage Chloroplasts: The Duplication of FtsZ Is Implicated in Endosymbiosis
inferredcites →https://doi.org/10.1007/s00425-009-1086-0openalex-snapshot
The speed of mitochondrial movement is regulated by the cytoskeleton and myosin in Picea wilsonii pollen tubes
inferredcites →https://doi.org/10.1007/s004250050606openalex-snapshot
The selective increase or decrease of organellar DNA in generative cells just after pollen mitosis one controls cytoplasmic inheritance
inferredcites →https://doi.org/10.1007/s00709-004-0073-3openalex-snapshot
Plastid stromules: video microscopy of their outgrowth, retraction, tensioning, anchoring, branching, bridging, and tip-shedding
inferredcites →https://doi.org/10.1007/s11248-007-9126-7openalex-snapshot
Visualisation of plastids in endosperm, pollen and roots of transgenic wheat expressing modified GFP fused to transit peptides from wheat SSU RubisCO, rice FtsZ and maize ferredoxin III proteins
inferredcites →https://doi.org/10.1016/j.ceb.2003.11.009openalex-snapshot
Cytoplasmic streaming in plants
inferredcites →https://doi.org/10.1016/j.cub.2005.01.013openalex-snapshot
A Novel Class of MYB Factors Controls Sperm-Cell Formation in Plants
inferredcites →https://doi.org/10.1016/j.cub.2008.12.018openalex-snapshot
Plant-Specific Protein MCD1 Determines the Site of Chloroplast Division in Concert with Bacteria-Derived MinD
inferredcites →https://doi.org/10.1016/j.febslet.2007.02.062openalex-snapshot
Plastid division coordination across a double‐membraned structure
inferredcites →https://doi.org/10.1016/j.pbi.2007.12.002openalex-snapshot
Plant growth and development — the new wave
inferredcites →https://doi.org/10.1016/j.pbi.2008.10.001openalex-snapshot
Plastid division: across time and space
inferredcites →https://doi.org/10.1016/s0022-5320(69)90033-1openalex-snapshot
A low-viscosity epoxy resin embedding medium for electron microscopy
inferredcites →https://doi.org/10.1016/s0074-7696(08)60415-5openalex-snapshot
The Division Apparatus of Plastids and Mitochondria
inferredcites →https://doi.org/10.1016/s0074-7696(08)61014-1openalex-snapshot
Controls to Plastid Division
inferredcites →https://doi.org/10.1016/s0960-9822(00)00466-8openalex-snapshot
A homologue of the bacterial cell division site-determining factor MinD mediates placement of the chloroplast division apparatus
inferredcites →https://doi.org/10.1038/nrmicro1290openalex-snapshot
Spatial control of bacterial division-site placement
inferredcites →https://doi.org/10.1046/j.1365-313x.1999.00500.xopenalex-snapshot
The distinctive roles of five different ARC genes in the chloroplast division process in Arabidopsis
inferredcites →https://doi.org/10.1046/j.1365-313x.2003.01705.xopenalex-snapshot
Automated whole mount localisation techniques for plant seedlings
inferredcites →https://doi.org/10.1073/pnas.0530206100openalex-snapshot
ARC5, a cytosolic dynamin-like protein from plants, is part of the chloroplast division machinery
inferredcites →https://doi.org/10.1073/pnas.95.8.4368openalex-snapshot
Plant nuclear gene knockout reveals a role in plastid division for the homolog of the bacterial cell division protein FtsZ, an ancestral tubulin
inferredcites →https://doi.org/10.1083/jcb.153.1.111openalex-snapshot
Ftsz Ring Formation at the Chloroplast Division Site in Plants
inferredcites →https://doi.org/10.1093/jxb/erj144openalex-snapshot
The suffulta mutation in tomato reveals a novel method of plastid replication during fruit ripening
inferredcites →https://doi.org/10.1093/jxb/ern321openalex-snapshot
Organelle motility in the pollen tube: a tale of 20 years
inferredcites →https://doi.org/10.1093/pcp/pcd037openalex-snapshot
Chloroplast Targeting, Distribution and Transcriptional Fluctuation of AtMinD1, a Eubacteria-Type Factor Critical for Chloroplast Division
inferredcites →https://doi.org/10.1093/pcp/pch186openalex-snapshot
DNA Interference: a Simple and Efficient Gene-Silencing System for High-Throughput Functional Analysis in the Fern Adiantum
inferredcites →https://doi.org/10.1093/pcp/pcm049openalex-snapshot
Effects of Mutations in Arabidopsis FtsZ1 on Plastid Division, FtsZ Ring Formation and Positioning, and FtsZ Filament Morphology in Vivo
inferredcites →https://doi.org/10.1093/pcp/pcn012openalex-snapshot
The Assembly of the FtsZ Ring at the Mid-Chloroplast Division Site Depends on a Balance Between the Activities of AtMinE1 and ARC11/AtMinD1
inferredcites →https://doi.org/10.1093/pcp/pcn084openalex-snapshot
Mitochondrial Dynamics in Plant Male Gametophyte Visualized by Fluorescent Live Imaging
inferredcites →https://doi.org/10.1093/pcp/pcp042openalex-snapshot
Visualization of Plastids in Pollen Grains: Involvement of FtsZ1 in Pollen Plastid Division
inferredcites →https://doi.org/10.1093/pcp/pcp047openalex-snapshot
Plant Cells Without Detectable Plastids are Generated in the crumpled leaf Mutant of Arabidopsis thaliana
inferredcites →https://doi.org/10.1093/pcp/pcp063openalex-snapshot
Live Imaging of Chloroplast FtsZ1 Filaments, Rings, Spirals, and Motile Dot Structures in the AtMinE1 Mutant and Overexpressor of Arabidopsis thaliana
inferredcites →https://doi.org/10.1104/pp.010386openalex-snapshot
A Chloroplast Protein Homologous to the Eubacterial Topological Specificity Factor MinE Plays a Role in Chloroplast Division
inferredcites →https://doi.org/10.1104/pp.116.2.797openalex-snapshot
Plastid Ontogeny during Petal Development in Arabidopsis1
inferredcites →https://doi.org/10.1104/pp.124.4.1668openalex-snapshot
Chloroplast Division and Morphology Are Differentially Affected by Overexpression of FtsZ1 and FtsZ2 Genes in Arabidopsis,
inferredcites →https://doi.org/10.1105/tpc.000836openalex-snapshot
Rab2 GTPase Regulates Vesicle Trafficking between the Endoplasmic Reticulum and the Golgi Bodies and Is Important to Pollen Tube Growth[W]
inferredcites →https://doi.org/10.1105/tpc.009373openalex-snapshot
A Plant-Specific Dynamin-Related Protein Forms a Ring at the Chloroplast Division Site
inferredcites →https://doi.org/10.1105/tpc.10.12.1991openalex-snapshot
Chloroplast Division in Higher Plants Requires Members of Two Functionally Divergent Gene Families with Homology to Bacterial ftsZ
inferredcites →https://doi.org/10.1105/tpc.105.030700openalex-snapshot
Arabidopsis Tic110 Is Essential for the Assembly and Function of the Protein Import Machinery of Plastids
inferredcites →https://doi.org/10.1105/tpc.105.033183openalex-snapshot
Rab11 GTPase-Regulated Membrane Trafficking Is Crucial for Tip-Focused Pollen Tube Growth in Tobacco
inferredcites →https://doi.org/10.1105/tpc.107.055756openalex-snapshot
EMB2473/MIRO1, anArabidopsisMiro GTPase, Is Required for Embryogenesis and Influences Mitochondrial Morphology in Pollen
inferredcites →https://doi.org/10.1105/tpc.109.067785openalex-snapshot
The PLASTID DIVISION1 and 2 Components of the Chloroplast Division Machinery Determine the Rate of Chloroplast Division in Land Plant Cell Differentiation
inferredcites →https://doi.org/10.1105/tpc.2.8.755openalex-snapshot
Early Flower Development 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/j.1399-3054.1962.tb08052.xopenalex-snapshot
A Revised Medium for Rapid Growth and Bio Assays with Tobacco Tissue Cultures
inferredcites →https://doi.org/10.1111/j.1751-1097.2008.00437.xopenalex-snapshot
Effects of arc3, arc5 and arc6 Mutations on Plastid Morphology and Stromule Formation in Green and Nongreen Tissues of Arabidopsis thaliana†
inferredcites →https://doi.org/10.1126/science.1129689openalex-snapshot
Isolated Chloroplast Division Machinery Can Actively Constrict After Stretching
inferredcites →https://doi.org/10.1186/1471-2229-4-6openalex-snapshot
A systemic gene silencing method suitable for high throughput, reverse genetic analyses of gene function in fern gametophytes
inferredcites →https://doi.org/10.1242/jcs.01092openalex-snapshot
Chloroplast division site placement requires dimerization of the ARC11/AtMinD1 protein in Arabidopsis
inferredcites →https://doi.org/10.1242/jcs.108.9.2937openalex-snapshot
Arc6, an extreme chloroplast division mutant of Arabidopsis also alters proplastid proliferation and morphology in shoot and root apices
inferredcites →https://doi.org/10.1242/jcs.113.1.81openalex-snapshot
Plastid tubules of higher plants are tissue-specific and developmentally regulated
inferredcites →https://doi.org/10.1242/jcs.99.1.21openalex-snapshot
Microtubule-determined plastid distribution during microsporogenesis in Lilium longiflorum
inferredcites →https://doi.org/10.1271/bbb.90309openalex-snapshot
Further Evaluation of the Localization and Functionality of Hemagglutinin Epitope- and Fluorescent Protein-Tagged AtMinD1 inArabidopsis thaliana
inferredcites →https://doi.org/10.1271/bbb.90473openalex-snapshot
Involvement ofAtMinE1in Plastid Morphogenesis in Various Tissues ofArabidopsis thaliana
inferredcites →https://doi.org/10.1371/journal.pone.0000718openalex-snapshot
An “Electronic Fluorescent Pictograph” Browser for Exploring and Analyzing Large-Scale Biological Data Sets
inferredcites →https://doi.org/10.1387/ijdb.051997elopenalex-snapshot
Plastids unleashed: their development and their integration in plant development
inferredcites →https://doi.org/10.1508/cytologia.66.113openalex-snapshot
Visualization of FtsZ Rings in Plastids of the Microspore in Lilium longiflorum.

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.4108857openalex-extracted
Representation of the Hyrcanian Forest (Northern Iran) in Modern Pollen Rain Revealed by Palynological and Metabarcoding Data
inferred← citeshttps://doi.org/10.1007/s00709-010-0168-yopenalex-snapshot
A green version of Haeckel’s rule
inferred← citeshttps://doi.org/10.1007/s00709-015-0935-xopenalex-snapshot
Visualisation of plastid degradation in sperm cells of wheat pollen
inferred← citeshttps://doi.org/10.1007/s00709-020-01503-2openalex-snapshot
Behavior of filamentous temperature-sensitive Z2 (FtsZ2) in the male gametophyte during sexual reproduction processes of flowering plants
inferred← citeshttps://doi.org/10.1007/s00709-020-01526-9openalex-snapshot
Tracking footprints of plastid evolution
inferred← citeshttps://doi.org/10.1016/j.fsigen.2015.12.010openalex-snapshot
Review and future prospects for DNA barcoding methods in forensic palynology
inferred← citeshttps://doi.org/10.1042/bst20221093openalex-snapshot
Visualizing the dynamics of plant energy organelles
inferred← citeshttps://doi.org/10.1080/15592324.2017.1343776openalex-snapshot
TheArabidopsis minDmutation causes aberrant FtsZ1 ring placement and moderate heterogeneity of chloroplasts in the leaf epidermis
inferred← citeshttps://doi.org/10.1105/tpc.111.088112openalex-snapshot
Two Mechanosensitive Channel Homologs Influence Division Ring Placement in Arabidopsis Chloroplasts
inferred← citeshttps://doi.org/10.1105/tpc.15.00180openalex-snapshot
Role of Aminoalcoholphosphotransferases 1 and 2 in Phospholipid Homeostasis in Arabidopsis
inferred← citeshttps://doi.org/10.1111/ppl.12648openalex-snapshot
Isolation and analysis of a stromule‐overproducing Arabidopsis mutant suggest the role of PARC6 in plastid morphology maintenance in the leaf epidermis
inferred← citeshttps://doi.org/10.1139/gen-2015-0200openalex-snapshot
Pollen DNA barcoding: current applications and future prospects
inferred← citeshttps://doi.org/10.1186/s12284-018-0206-5openalex-snapshot
Heat stress induces spikelet sterility in rice at anthesis through inhibition of pollen tube elongation interfering with auxin homeostasis in pollinated pistils
inferred← citeshttps://doi.org/10.1271/kagakutoseibutsu.62.570openalex-snapshot
Stromules: Tubular Structures Extending from Plastids
inferred← citeshttps://doi.org/10.3389/fpls.2015.00823openalex-snapshot
The Arabidopsis minE mutation causes new plastid and FtsZ1 localization phenotypes in the leaf epidermis
inferred← citeshttps://doi.org/10.35535/acpa-2023-0007openalex-snapshot
Representation of the Hyrcanian forest (northern Iran) in modern pollen rain revealed by palynological and DNA-metabarcoding data
inferred← citeshttps://doi.org/10.4161/15592324.2014.977200openalex-snapshot
Pollen tube growth: where does the energy come from?
inferred← citeshttps://doi.org/10.4161/psb.7.1.18484openalex-snapshot
Visualization of plastid movement in the pollen tube ofArabidopsis thaliana
inferred← citeshttps://doi.org/10.53846/goediss-9622openalex-snapshot
Long-term vegetation dynamics along altitudinal and longitudinal gradients in the Hyrcanian forest region (northern Iran)
inferred← citeshttps://doi.org/10.5586/asbp/196668openalex-snapshot
Plasmodial tapetum, orbicules, and ultrastructure of Myosotis scorpioides L. (Boraginaceae) pollen grains
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