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  • Xerobranching manuscript_12-07

    Rights statement: This is the author’s version of a work that was accepted for publication in Current Biology. Changes resulting from the publishing process, such as peer review, editing, corrections, structural formatting, and other quality control mechanisms may not be reflected in this document. Changes may have been made to this work since it was submitted for publication. A definitive version was subsequently published in Current Biology, 28,19, 2018 DOI: 10.1016/j.cub.2018.07.074

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    Available under license: CC BY-NC-ND: Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License

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The xerobranching response represses lateral root formation when roots are not in contact with water

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  • Beata Orman-Ligeza
  • Emily C. Morris
  • Boris Parizot
  • Tristan Livigne
  • Aurelie Babe
  • Aleksander Ligeza
  • Stephanie Klein
  • Craig D. Sturrock
  • Wei Xuan
  • Ondřey Novák
  • Karin Ljung
  • Maria Fernandez
  • Pedro L. Rodriguez
  • Ive De Smit
  • Francois Chaumont
  • Henri Batoko
  • Claire Périlleux
  • Jonathan P. Lynch
  • Malcolm J. Bennett
  • Tom Beeckman
  • Xavier Draye
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<mark>Journal publication date</mark>10/2018
<mark>Journal</mark>Current Biology
Issue number19
Volume28
Number of pages9
Pages (from-to)3165-3173
Publication StatusPublished
<mark>Original language</mark>English

Abstract

Efficient soil exploration by roots represents an important target for crop improvement and food security [1, 2]. Lateral root (LR) formation is a key trait for optimising soil foraging for crucial resources such as water and nutrients. Here, we report an adaptive response termed xerobranching, exhibited by cereal roots, that represses branching when root tips are not in contact with wet soil. Non-invasive X-ray microCT imaging revealed that cereal roots rapidly
repress LR formation as they enter an air space within a soil profile and are no longer in contact with water. Transcript profiling of cereal root tips revealed that transient water deficit triggers the abscisic acid (ABA) response pathway. In agreement with this, exogenous ABA treatment can mimic repression of LR formation under transient water deficit. Genetic analysis in Arabidopsis revealed that ABA repression of LR formation requires the PYR/PYL/RCARdependent signalling pathway. Our findings suggest that ABA acts as the key signal regulating xerobranching. We conclude that this new ABA-dependent adaptive mechanism allows roots to rapidly respond to changes in water
availability in their local micro-environment and to use internal resources efficiently.

Bibliographic note

This is the author’s version of a work that was accepted for publication in Current Biology. Changes resulting from the publishing process, such as peer review, editing, corrections, structural formatting, and other quality control mechanisms may not be reflected in this document. Changes may have been made to this work since it was submitted for publication. A definitive version was subsequently published in Current Biology, 28,19, 2018 DOI: 10.1016/j.cub.2018.07.074