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Tissue specific auxin biosynthesis regulates leaf vein patterning

https://doi.org/10.1101/184275
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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/wdev.195openalex-snapshot
The wing and the eye: a parsimonious theory for scaling and growth control?
inferredcites →https://doi.org/10.1007/bf00387102openalex-snapshot
1-N-naphthylphthalamic acid and 2,3,5-triiodobenzoic acid
inferredcites →https://doi.org/10.1007/bf00551271openalex-snapshot
Structure and mechanics of the iris leaf
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.2008.01.049openalex-snapshot
Rapid Synthesis of Auxin via a New Tryptophan-Dependent Pathway Is Required for Shade Avoidance in Plants
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.2014.03.014openalex-snapshot
Physical Forces Regulate Plant Development and Morphogenesis
inferredcites →https://doi.org/10.1016/j.jbiomech.2004.09.027openalex-snapshot
Biomechanics of cellular solids
inferredcites →https://doi.org/10.1016/j.jtbi.2014.03.005openalex-snapshot
Canalization-based vein formation in a growing leaf
inferredcites →https://doi.org/10.1038/nature13663openalex-snapshot
PLETHORA gradient formation mechanism separates auxin responses
inferredcites →https://doi.org/10.1038/ncomms6833openalex-snapshot
Arabidopsis ERF109 mediates cross-talk between jasmonic acid and auxin biosynthesis during lateral root formation
inferredcites →https://doi.org/10.1038/nrm3169openalex-snapshot
Understanding morphogenetic growth control — lessons from flies
inferredcites →https://doi.org/10.1073/pnas.0807814105openalex-snapshot
Mechanical induction of lateral root initiation in Arabidopsis thaliana
inferredcites →https://doi.org/10.1073/pnas.1108434108openalex-snapshot
The main auxin biosynthesis pathway in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.1108436108openalex-snapshot
Conversion of tryptophan to indole-3-acetic acid by TRYPTOPHAN AMINOTRANSFERASES OF ARABIDOPSIS and YUCCAs in Arabidopsis
inferredcites →https://doi.org/10.1093/jxb/eru433openalex-snapshot
Complementation of the embryo-lethal T-DNA insertion mutant of AUXIN-BINDING-PROTEIN 1 (ABP1) with abp1 point mutated versions reveals crosstalk of ABP1 and phytochromes
inferredcites →https://doi.org/10.1093/jxb/erv024openalex-snapshot
A novel method of measuring leaf epidermis and mesophyll stiffness shows the ubiquitous nature of the sandwich structure of leaf laminas in broad-leaved angiosperm species
inferredcites →https://doi.org/10.1093/mp/ssr104openalex-snapshot
Auxin Biosynthesis: A Simple Two-Step Pathway Converts Tryptophan to Indole-3-Acetic Acid in Plants
inferredcites →https://doi.org/10.1098/rspb.1980.0109openalex-snapshot
The dynamics of auxin transport
inferredcites →https://doi.org/10.1098/rstb.1981.0154openalex-snapshot
The polar transport of auxin and vein patterns in plants
inferredcites →https://doi.org/10.1101/cshperspect.a001446openalex-snapshot
Cellular Responses to Auxin: Division versus Expansion
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.1415106openalex-snapshot
Auxin biosynthesis by the YUCCA flavin monooxygenases controls the formation of floral organs and vascular tissues in Arabidopsis
inferredcites →https://doi.org/10.1101/gad.1426606openalex-snapshot
Polar auxin transport and patterning: grow with the flow
inferredcites →https://doi.org/10.1101/gad.497009openalex-snapshot
Integration of transport-based models for phyllotaxis and midvein formation
inferredcites →https://doi.org/10.1104/pp.003228openalex-snapshot
Indole Acetic Acid Distribution Coincides with Vascular Differentiation Pattern during Arabidopsis Leaf Ontogeny
inferredcites →https://doi.org/10.1104/pp.013623openalex-snapshot
Auxin Signaling in Arabidopsis Leaf Vascular Development
inferredcites →https://doi.org/10.1104/pp.103.032300openalex-snapshot
Long-Term Inhibition by Auxin of Leaf Blade Expansion in Bean and Arabidopsis
inferredcites →https://doi.org/10.1104/pp.110.167619openalex-snapshot
VirtualLeaf: An Open-Source Framework for Cell-Based Modeling of Plant Tissue Growth and Development
inferredcites →https://doi.org/10.1104/pp.111.185066openalex-snapshot
Key Proliferative Activity in the Junction between the Leaf Blade and Leaf Petiole of Arabidopsis
inferredcites →https://doi.org/10.1104/pp.121.4.1179openalex-snapshot
Auxin Is Required for Leaf Vein Pattern in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.15.01540openalex-snapshot
Novel Vein Patterns in Arabidopsis Induced by Small Molecules
inferredcites →https://doi.org/10.1105/tpc.004960openalex-snapshot
Auxin-Mediated Cell Cycle Activation during Early Lateral Root Initiation
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.109.068841openalex-snapshot
NO VEIN Mediates Auxin-Dependent Specification and Patterning in theArabidopsisEmbryo, Shoot, and Root
inferredcites →https://doi.org/10.1105/tpc.111.088047openalex-snapshot
The Arabidopsis YUCCA1 Flavin Monooxygenase Functions in the Indole-3-Pyruvic Acid Branch of Auxin Biosynthesis
inferredcites →https://doi.org/10.1105/tpc.15.01057openalex-snapshot
The Effects of High Steady State Auxin Levels on Root Cell Elongation in Brachypodium
inferredcites →https://doi.org/10.1105/tpc.3.7.677openalex-snapshot
Requirement of the Auxin Polar Transport System in Early Stages of Arabidopsis Floral Bud Formation.
inferredcites →https://doi.org/10.1111/j.1365-313x.2005.02581.xopenalex-snapshot
Reviewing models of auxin canalization in the context of leaf vein pattern formation in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1461-0248.2010.01554.xopenalex-snapshot
Venation networks and the origin of the leaf economics spectrum
inferredcites →https://doi.org/10.1111/j.1469-8137.1984.tb03572.xopenalex-snapshot
REPLACEMENT OF LEAF PRIMORDIA WITH IAA IN THE INDUCTION OF VASCULAR DIFFERENTIATION IN THE STEM OF COLUCUS
inferredcites →https://doi.org/10.1111/tpj.12399openalex-snapshot
Yucasin is a potent inhibitor of YUCCA , a key enzyme in auxin biosynthesis
inferredcites →https://doi.org/10.1126/science.1123542openalex-snapshot
PIN Proteins Perform a Rate-Limiting Function in Cellular Auxin Efflux
inferredcites →https://doi.org/10.1126/science.1165594openalex-snapshot
Developmental Patterning by Mechanical Signals in Arabidopsis
inferredcites →https://doi.org/10.1126/science.1255215openalex-snapshot
Integration of growth and patterning during vascular tissue formation in Arabidopsis
inferredcites →https://doi.org/10.1126/science.282.5397.2226openalex-snapshot
Regulation of Polar Auxin Transport by AtPIN1 in Arabidopsis Vascular Tissue
inferredcites →https://doi.org/10.1242/dev.01182openalex-snapshot
Stage-specific markers define early steps of procambium development inArabidopsisleaves and correlate termination of vein formation with mesophyll differentiation
inferredcites →https://doi.org/10.1242/dev.126.13.2979openalex-snapshot
Responses of plant vascular systems to auxin transport inhibition
inferredcites →https://doi.org/10.1371/journal.pgen.1003294openalex-snapshot
Patterning of Leaf Vein Networks by Convergent Auxin Transport Pathways
inferredcites →https://doi.org/10.1371/journal.pgen.1003759openalex-snapshot
The Arabidopsis IDD14, IDD15, and IDD16 Cooperatively Regulate Lateral Organ Morphogenesis and Gravitropism by Promoting Auxin Biosynthesis and Transport
inferredcites →https://doi.org/10.1371/journal.pone.0118238openalex-snapshot
Self-Organization of Plant Vascular Systems: Claims and Counter-Claims about the Flux-Based Auxin Transport Model
inferredcites →https://doi.org/10.7554/elife.18165openalex-snapshot
Formation of polarity convergences underlying shoot outgrowths
inferredcites →https://doi.org/10.7554/elife.19048openalex-snapshot
TIR1/AFB-Aux/IAA auxin perception mediates rapid cell wall acidification and growth of Arabidopsis hypocotyls

What points at this work

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

inferred← citeshttps://doi.org/10.1007/s00299-018-2319-0openalex-snapshot
Auxin-mediated regulation of vascular patterning in Arabidopsis thaliana leaves
inferred← citeshttps://doi.org/10.1007/s13205-023-03709-6openalex-snapshot
Recent advances in auxin biosynthesis and homeostasis
inferred← citeshttps://doi.org/10.1016/j.molp.2018.12.012openalex-snapshot
Auxin EvoDevo: Conservation and Diversification of Genes Regulating Auxin Biosynthesis, Transport, and Signaling
inferred← citeshttps://doi.org/10.1101/783480openalex-snapshot
A dynamic pattern of local auxin sources is required for root regeneration
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