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A dynamic pattern of local auxin sources is required for root regeneration

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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/bf00393230openalex-snapshot

The de novo origin of the quiescent center regenerating root apices of Zea mays

inferredcites →https://doi.org/10.1016/j.cell.2008.01.047openalex-snapshot

TAA1-Mediated Auxin Biosynthesis Is Essential for Hormone Crosstalk and Plant Development

inferredcites →https://doi.org/10.1016/j.cell.2016.04.046openalex-snapshot

Root Regeneration Triggers an Embryo-like Sequence Guided by Hormonal Interactions

inferredcites →https://doi.org/10.1016/j.cell.2019.03.006openalex-snapshot

A Jasmonate Signaling Network Activates Root Stem Cells and Promotes Regeneration

inferredcites →https://doi.org/10.1016/j.cub.2005.09.052openalex-snapshot

Patterns of Auxin Transport and Gene Expression during Primordium Development Revealed by Live Imaging of the Arabidopsis Inflorescence Meristem

inferredcites →https://doi.org/10.1016/j.cub.2013.09.039openalex-snapshot

Local Auxin Sources Orient the Apical-Basal Axis in Arabidopsis Embryos

inferredcites →https://doi.org/10.1016/j.cub.2014.10.064openalex-snapshot

Detecting Regular Sound Changes in Linguistics as Events of Concerted Evolution

inferredcites →https://doi.org/10.1016/j.cub.2015.02.022openalex-snapshot

PLETHORA Genes Control Regeneration by a Two-Step Mechanism

inferredcites →https://doi.org/10.1016/j.devcel.2018.09.022openalex-snapshot

Local Auxin Biosynthesis Is a Key Regulator of Plant Development

inferredcites →https://doi.org/10.1016/s0092-8674(00)81535-4openalex-snapshot

An Auxin-Dependent Distal Organizer of Pattern and Polarity in the Arabidopsis Root

inferredcites →https://doi.org/10.1023/a:1016586401506openalex-snapshot

Indole-3-acetic acid biosynthesis in isolated axes from germinating bean seeds: The effect of wounding on the biosynthetic pathway

inferredcites →https://doi.org/10.1038/nature03184openalex-snapshot

The PIN auxin efflux facilitator network controls growth and patterning in Arabidopsis roots

inferredcites →https://doi.org/10.1038/nature06215openalex-snapshot

Auxin transport is sufficient to generate a maximum and gradient guiding root growth

inferredcites →https://doi.org/10.1038/nature07597openalex-snapshot

Organ regeneration does not require a functional stem cell niche in plants

inferredcites →https://doi.org/10.1038/nplants.2016.165openalex-snapshot

The heterodimeric transcription factor complex ERF115–PAT1 grants regeneration competence

inferredcites →https://doi.org/10.1038/nrm3790openalex-snapshot

Plant and animal stem cells: similar yet different

inferredcites →https://doi.org/10.1038/s41598-017-14332-wopenalex-snapshot

Yucasin DF, a potent and persistent inhibitor of auxin biosynthesis in plants

inferredcites →https://doi.org/10.1038/s41598-018-23276-8openalex-snapshot

Three-dimensional Epigenome Statistical Model: Genome-wide Chromatin Looping Prediction

inferredcites →https://doi.org/10.1038/s41598-018-24452-6openalex-snapshot

Multifunctional activities of ERF109 as affected by salt stress in Arabidopsis

inferredcites →https://doi.org/10.1073/pnas.0708506104openalex-snapshot

NPY1, a BTB-NPH3-like protein, plays a critical role in auxin-regulated organogenesis in Arabidopsis

inferredcites →https://doi.org/10.1093/jxb/erv256openalex-snapshot

The importance of localized auxin production for morphogenesis of reproductive organs and embryos inArabidopsis

inferredcites →https://doi.org/10.1093/jxb/erw213openalex-snapshot

YUCCA -mediated auxin biogenesis is required for cell fate transition occurring during de novo root organogenesis in Arabidopsis

inferredcites →https://doi.org/10.1093/pcp/pcu039openalex-snapshot

Auxin Overproduction in Shoots Cannot Rescue Auxin Deficiencies in Arabidopsis Roots

inferredcites →https://doi.org/10.1093/pcp/pcx107openalex-snapshot

YUCCA9-Mediated Auxin Biosynthesis and Polar Auxin Transport Synergistically Regulate Regeneration of Root Systems Following Root Cutting

inferredcites →https://doi.org/10.1093/pcp/pcx172openalex-snapshot

A Conceptual Framework for Cell Identity Transitions in Plants

inferredcites →https://doi.org/10.1093/pcp/pcz156openalex-snapshot

A Positive Feedback Loop Comprising LHW–TMO5 and Local Auxin Biosynthesis Regulates Initial Vascular Development in Arabidopsis Roots

inferredcites →https://doi.org/10.1101/184275openalex-snapshot

Tissue specific auxin biosynthesis regulates leaf vein patterning

inferredcites →https://doi.org/10.1101/gad.1402406openalex-snapshot

Control of leaf vascular patterning by polar auxin transport

inferredcites →https://doi.org/10.1101/gad.905201openalex-snapshot

BIG: a calossin-like protein required for polar auxin transport in Arabidopsis

inferredcites →https://doi.org/10.1104/pp.012740openalex-snapshot

Do Phytotropins Inhibit Auxin Efflux by Impairing Vesicle Traffic?

inferredcites →https://doi.org/10.1104/pp.17.00980openalex-snapshot

Regulation of Hormonal Control, Cell Reprogramming, and Patterning during De Novo Root Organogenesis

inferredcites →https://doi.org/10.1105/tpc.109.066480openalex-snapshot

An Auxin Gradient and Maximum in the Arabidopsis Root Apex Shown by High-Resolution Cell-Specific Analysis of IAA Distribution and Synthesis

inferredcites →https://doi.org/10.1105/tpc.111.089029openalex-snapshot

A Small-Molecule Screen Identifies l -Kynurenine as a Competitive Inhibitor of TAA1/TAR Activity in Ethylene-Directed Auxin Biosynthesis and Root Growth in Arabidopsis

inferredcites →https://doi.org/10.1105/tpc.114.133595openalex-snapshot

The Yin-Yang of Hormones: Cytokinin and Auxin Interactions in Plant Development

inferredcites →https://doi.org/10.1105/tpc.114.134874openalex-snapshot

PIN-Dependent Auxin Transport: Action, Regulation, and Evolution

inferredcites →https://doi.org/10.1105/tpc.16.00656openalex-snapshot

The PLETHORA Gene Regulatory Network Guides Growth and Cell Differentiation in Arabidopsis Roots

inferredcites →https://doi.org/10.1105/tpc.7.10.1611openalex-snapshot

Composite Structure of Auxin Response Elements

inferredcites →https://doi.org/10.1126/science.1121790openalex-snapshot

A Molecular Framework for Plant Regeneration

inferredcites →https://doi.org/10.1126/science.1146265openalex-snapshot

A High-Resolution Root Spatiotemporal Map Reveals Dominant Expression Patterns

inferredcites →https://doi.org/10.1126/science.1240667openalex-snapshot

ERF115 Controls Root Quiescent Center Cell Division and Stem Cell Replenishment

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-042817-040226openalex-snapshot

Essential Roles of Local Auxin Biosynthesis in Plant Development and in Adaptation to Environmental Changes

inferredcites →https://doi.org/10.1146/annurev-arplant-043015-112122openalex-snapshot

Transcriptional Responses to the Auxin Hormone

inferredcites →https://doi.org/10.1242/dev.00596openalex-snapshot

Microsurgical and laser ablation analysis of interactions between the zones and layers of the tomato shoot apical meristem

inferredcites →https://doi.org/10.1242/dev.127.3.595openalex-snapshot

Molecular analysis of SCARECROW function reveals a radial patterning mechanism common to root and shoot

inferredcites →https://doi.org/10.1371/journal.pgen.1005944openalex-snapshot

Glucocerebrosidase Deficiency in Drosophila Results in α-Synuclein-Independent Protein Aggregation and Neurodegeneration

inferredcites →https://doi.org/10.1371/journal.pone.0005553openalex-snapshot

Golden Gate Shuffling: A One-Pot DNA Shuffling Method Based on Type IIs Restriction Enzymes

inferredcites →https://doi.org/10.3389/fpls.2014.00208openalex-snapshot

A simple method suitable to study de novo root organogenesis

inferredcites →https://doi.org/10.3389/fpls.2014.00692openalex-snapshot

Strategies for transferring resistance into wheat: from wide crosses to GM cassettes

inferredcites →https://doi.org/10.3389/fpls.2016.00381openalex-snapshot

Plant Hormone Homeostasis, Signaling, and Function during Adventitious Root Formation in Cuttings

inferredcites →https://doi.org/10.3389/fpls.2016.01509openalex-snapshot

GOLDEN 2-LIKE Transcription Factors of Plants

inferredcites →https://doi.org/10.7554/elife.51061openalex-snapshot

Coordination of tissue cell polarity by auxin transport and signaling

What points at this work

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

inferred← citeshttps://doi.org/10.1007/s00239-021-10005-5openalex-snapshot

Molecular Evolution and Local Root Heterogeneous Expression of the Chenopodium quinoa ARF Genes Provide Insights into the Adaptive Domestication of Crops in Complex Environments

inferred← citeshttps://doi.org/10.1016/j.pbi.2019.12.007openalex-snapshot

Regrowing the damaged or lost body parts

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