Abstract

Plants display remarkable abilities to adjust growth and development to environmental conditions, such as the amount of available water. This developmental plasticity is apparent not only in root and shoot growth rates, but also in tissue patterning and cell morphology.1,2 We have previously shown that in response to limited water availability, Arabidopsis thaliana root displays changes in xylem morphology, mediated by the non-cell-autonomous action of abscisic acid, ABA.2 Here, we show, through analyses of ABA response reporters and tissue-specific suppression of ABA signaling, that xylem cells themselves act as primary signaling centers governing both xylem cell fate and xylem differentiation rate, revealing the cell-autonomous control of multiple aspects of xylem development by ABA. ABA rapidly activates the expression of genes encoding VASCULAR-RELATED NAC DOMAIN (VND) transcription factors. Molecular and genetic analyses revealed that the two ABA-mediated xylem developmental changes are regulated by distinct members of this transcription factor family, with VND2 and VND3 promoting differentiation rate of metaxylem cells, while VND7 promotes the conversion of metaxylem toward protoxylem morphology. This phenomenon shows how different aspects of developmental plasticity can be interlinked, yet genetically separable. Moreover, similarities in phenotypic and molecular responses to ABA in diverse species indicate evolutionary conservation of the ABA-xylem development regulatory network among eudicots. Hence, this study gives molecular insights into how environmental stress modifies plant vascular anatomy and has potential relevance for water use optimization and adaptation to drought conditions.

Highlights

  • ABA affects both xylem cell fate and differentiation rate Water-limiting conditions trigger the formation of multiple protoxylem-like cells with spiral secondary cell walls (SCWs) in place of metaxylem with pitted SCWs (Figures 1A–1C, 1E, and S1B).[2,3]. This effect is partly dependent on endodermal abscisic acid (ABA) signaling resulting in enhanced levels of microRNA165, which acts non-cell-autonomously to suppress target HOMEODOMAIN-LEUCINE ZIPPER class III (HD-ZIPIII) transcription factors within the stele, promoting protoxylem over metaxylem cell fate.[4,5]

  • To further assess ABA’s effect on xylem formation, we analyzed if it could affect xylem differentiation rate by measuring the distance from root tip to point of lignified SCWs detected in wild type (Col-0) after treatment with 1 mM ABA

  • While mocktreated J0571>>abi[1] occasionally displayed discontinuous metaxylem,[2] this was not detected in either of the stele-active lines (Figures S2B and S2C). These results suggest that ABA signaling in the stele is not critical for xylem formation per se, but that signaling within the xylem cells is essential to determine both xylem differentiation rate and xylem cell fate upon conditions causing elevated ABA levels

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Summary

Introduction

After 48 h 1 mM ABA treatment, 94% displayed differentiated imx at 7 mm from the root tip (Figure 1H), suggesting that ABA promotes metaxylem differentiation rate independent of its effect on xylem morphology. The dominant ABA-INSENSITIVE1 mutant (abi1-1), in which ABA signaling is suppressed even in the presence of ABA,[6,7] strongly reduced the effects of ABA treatment on early imx differentiation (20% in abi[1] versus 94% in wild type; Figures 1D, 1I, and S1C), and on xylem fate change in omx (Figure S1G),[2] showing that canonical ABA signaling is important for xylem differentiation.

Results
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