ArticleFrontiers in plant science2014
A model for an early role of auxin in Arabidopsis gynoecium morphogenesis.
Article in Frontiers in plant science, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.
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27 citing papers in PubMed, 48 citations in OpenAlex.
- A two-step auxin-GA cross-talk regulates organ formation in tomato.Development (Cambridge, England) · 2026Article
- RNA-Seq Analysis Reveals Potential Genes Involved in Plant Growth Regulator-Induced Ovary Development in Male Kiwifruit (Plants (Basel, Switzerland) · 2025Article
- Gene Regulatory Network Controlling Flower Development in Spinach (International journal of molecular sciences · 2024Article
- Two orthogonal differentiation gradients locally coordinate fruit morphogenesis.Nature communications · 2024Article
- Comparative Transcriptome Analysis Points to the Biological Processes of Hybrid Incompatibility betweenPlants (Basel, Switzerland) · 2023Article
- A model worker: Multifaceted modulation of AUXIN RESPONSE FACTOR3 orchestrates plant reproductive phases.Frontiers in plant science · 2023Review
- Review
- The Relationship between AGAMOUS and Cytokinin Signaling in the Establishment of Carpeloid Features.Plants (Basel, Switzerland) · 2021Article
- Comprehensive Analysis and Expression Profiling of PIN, AUX/LAX, and ABCB Auxin Transporter Gene Families inBiology · 2021Article
- Auxin and Flower Development: A Blossoming Field.Cold Spring Harbor perspectives in biology · 2021Review
- Article
- A galling insect activates plant reproductive programs during gall development.Scientific reports · 2019Article
- Auxin regulation involved in gynoecium morphogenesis of papaya flowers.Horticulture research · 2019Article
- Evidence for the Regulation of Gynoecium Morphogenesis byPlant physiology · 2018Article
- Class XI Myosins Contribute to Auxin Response and Senescence-Induced Cell Death inFrontiers in plant science · 2018Article
- Cytokinin-Auxin Crosstalk in the Gynoecial Primordium Ensures Correct Domain Patterning.Plant physiology · 2017Article
- Fine-tuning of auxin homeostasis governs the transition from floral stem cell maintenance to gynoecium formation.Nature communications · 2017Article
- Genome-wide analysis of auxin transport genes identifies the hormone responsive patterns associated with leafy head formation in Chinese cabbage.Scientific reports · 2017Article
- MicroRNA 157-targeted SPL genes regulate floral organ size and ovule production in cotton.BMC plant biology · 2017Article
- Article
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Authors and funding
2 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
The female reproductive organ of angiosperms, the gynoecium, often consists of the fusion of multiple ovule-bearing carpels. It serves the important function of producing and protecting ovules as well as mediating pollination. The gynoecium has likely contributed to the tremendous success of angiosperms over their 160 million year history. In addition, being a highly complex plant organ, the gynoecium is well suited to serving as a model system for use in the investigation of plant morphogenesis and development. The longstanding model of gynoecium morphogenesis in Arabidopsis holds that apically localized auxin biosynthesis in the gynoecium results in an apical to basal gradient of auxin that serves to specify along its length the development of style, ovary, and gynophore in a concentration-dependent manner. This model is based primarily on the observed effects of the auxin transport blocker N-1-naphthylphthalamic acid (NPA) as well as analyses of mutants of Auxin Response Factor (ARF) 3/ETTIN (ETT). Both NPA treatment and ett mutation disrupt gynoecium morphological patterns along the apical-basal axis. More than a decade after the model's initial proposal, however, the auxin gradient on which the model critically depends remains elusive. Furthermore, multiple observations are inconsistent with such an auxin-gradient model. Chiefly, the timing of gynoecium emergence and patterning occurs at a very early stage when the organ has little-to-no apical-basal dimension. Based on these observations and current models of early leaf patterning, we propose an alternate model for gynoecial patterning. Under this model, the action of auxin is necessary for the early establishment of adaxial-abaxial patterning of the carpel primordium. In this case, the observed gynoecial phenotypes caused by NPA and ett are due to the disruption of this early adaxial-abaxial patterning of the carpel primordia. Here we present the case for this model based on recent literature and current models of leaf development.
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