Abstract

SummaryTissue-wide polarity fields, in which cell polarity is coordinated across the tissue, have been described for planar organs such as the Drosophila wing and are considered important for coordinating growth and differentiation [1]. In planar plant organs, such as leaves, polarity fields have been identified for subgroups of cells, such as stomatal lineages [2], trichomes [3, 4], serrations [5], or early developmental stages [6]. Here, we show that ectopic induction of the stomatal protein BASL (BREAKING OF ASYMMETRY IN THE STOMATAL LINEAGE) reveals a tissue-wide epidermal polarity field in leaves throughout development. Ectopic GFP-BASL is typically localized toward the proximal end of cells and to one lobe of mature pavement cells, revealing a polarity field that aligns with the proximodistal axis of the leaf (base to tip). The polarity field is largely parallel to the midline of the leaf but diverges in more lateral positions, particularly at later stages in development, suggesting it may be deformed during growth. The polarity field is observed in the speechless mutant, showing that it is independent of stomatal lineages, and is observed in isotropic cells, showing that cell shape anisotropy is not required for orienting polarity. Ectopic BASL forms convergence and divergence points at serrations, mirroring epidermal PIN polarity patterns, suggesting a common underlying polarity mechanism. Thus, we show that similar to the situation in animals, planar plant organs have a tissue-wide cell polarity field, and this may provide a general cellular mechanism for guiding growth and differentiation.

Highlights

  • Evidence for a tissuewide polarity field maintained during planar plant organ development has been lacking

  • Several proteins preferentially localized to one end of the cell have been described in plants, including PIN-FORMED (PIN) proteins, BASL (BREAKING OF ASYMMETRY IN THE STOMATAL LINEAGE), BRXL2 (BREVIS RADIX-LIKE 2), POLAR (POLAR LOCALIZATION DURING ASMMETRIC DIVISION AND REDISTRIBUTION), OCTOPUS, BORs (BORON TRANSPORTERS 1), and NIPs (NODULIN26LIKE INTRINSIC PROTEINS) [2, 10,11,12,13,14]

  • PIN1 is preferentially localized at the distal end of cells in leaf primordia, but this pattern disappears at later developmental stages [6, 15]

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Summary

Introduction

Several proteins preferentially localized to one end of the cell (i.e., exhibiting cell polarity) have been described in plants, including PIN-FORMED (PIN) proteins, BASL (BREAKING OF ASYMMETRY IN THE STOMATAL LINEAGE), BRXL2 (BREVIS RADIX-LIKE 2), POLAR (POLAR LOCALIZATION DURING ASMMETRIC DIVISION AND REDISTRIBUTION), OCTOPUS, BORs (BORON TRANSPORTERS 1), and NIPs (NODULIN26LIKE INTRINSIC PROTEINS) [2, 10,11,12,13,14]. BRXL2 shows preferential localization to the proximal end of cells in the stomatal lineage [2], compounded by a spiral pattern of polarity switching involved in stomatal spacing [16

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