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1.
Development ; 147(13)2020 07 06.
Article in English | MEDLINE | ID: mdl-32493758

ABSTRACT

Unlike in animals, in plants, vein patterning does not rely on direct cell-cell interaction and cell migration; instead, it depends on the transport of the plant hormone auxin, which in turn depends on the activity of the PIN-FORMED1 (PIN1) auxin transporter. The current hypotheses of vein patterning by auxin transport propose that, in the epidermis of the developing leaf, PIN1-mediated auxin transport converges to peaks of auxin level. From those convergence points of epidermal PIN1 polarity, auxin would be transported in the inner tissues where it would give rise to major veins. Here, we have tested predictions of this hypothesis and have found them unsupported: epidermal PIN1 expression is neither required nor sufficient for auxin transport-dependent vein patterning, whereas inner-tissue PIN1 expression turns out to be both required and sufficient for auxin transport-dependent vein patterning. Our results refute all vein patterning hypotheses based on auxin transport from the epidermis and suggest alternatives for future tests.


Subject(s)
Indoleacetic Acids/metabolism , Arabidopsis/metabolism , Arabidopsis Proteins/genetics , Arabidopsis Proteins/metabolism , Biological Transport/physiology , Gene Expression Regulation, Plant/genetics , Gene Expression Regulation, Plant/physiology , Membrane Transport Proteins/metabolism , Plant Leaves/metabolism
2.
Dev Dyn ; 249(9): 1127-1146, 2020 09.
Article in English | MEDLINE | ID: mdl-32319191

ABSTRACT

BACKGROUND: Understanding developmental processes requires the unambiguous identification of cells and tissues, and the selective manipulation of the properties of those cells and tissues. Both requirements can most efficiently be satisfied through the use of GAL4/GFP enhancer-trap lines. No such lines, however, have been characterized for the study of early leaf development in the Columbia-0 reference genotype of Arabidopsis. RESULTS: Here we address this limitation by identifying and characterizing a set of GAL4/GFP enhancer-trap lines in the Columbia-0 background for the specific labeling of cells and tissues during early leaf development, and for the targeted expression of genes of interest in those cells and tissues. CONCLUSIONS: By using one line in our set to address outstanding questions in leaf vein patterning, we show that these lines can be used to address key questions in plant developmental biology.


Subject(s)
Arabidopsis , Enhancer Elements, Genetic , Gene Expression Regulation, Plant , Green Fluorescent Proteins , Plant Leaves , Plants, Genetically Modified , Arabidopsis/embryology , Arabidopsis/genetics , Green Fluorescent Proteins/biosynthesis , Green Fluorescent Proteins/genetics , Place Cells/metabolism , Plant Leaves/embryology , Plant Leaves/genetics , Plants, Genetically Modified/embryology , Plants, Genetically Modified/genetics
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