Antigravitropic PIN polarization maintains non-vertical growth in lateral roots

Nat Plants. 2023 Sep;9(9):1500-1513. doi: 10.1038/s41477-023-01478-x. Epub 2023 Sep 4.

Abstract

Lateral roots are typically maintained at non-vertical angles with respect to gravity. These gravitropic setpoint angles are intriguing because their maintenance requires that roots are able to effect growth response both with and against the gravity vector, a phenomenon previously attributed to gravitropism acting against an antigravitropic offset mechanism. Here we show how the components mediating gravitropism in the vertical primary root-PINs and phosphatases acting upon them-are reconfigured in their regulation such that lateral root growth at a range of angles can be maintained. We show that the ability of Arabidopsis lateral roots to bend both downward and upward requires the generation of auxin asymmetries and is driven by angle-dependent variation in downward gravitropic auxin flux acting against angle-independent upward, antigravitropic flux. Further, we demonstrate a symmetry in auxin distribution in lateral roots at gravitropic setpoint angle that can be traced back to a net, balanced polarization of PIN3 and PIN7 auxin transporters in the columella. These auxin fluxes are shifted by altering PIN protein phosphoregulation in the columella, either by introducing PIN3 phosphovariant versions or via manipulation of levels of the phosphatase subunit PP2A/RCN1. Finally, we show that auxin, in addition to driving lateral root directional growth, acts within the lateral root columella to induce more vertical growth by increasing RCN1 levels, causing a downward shift in PIN3 localization, thereby diminishing the magnitude of the upward, antigravitropic auxin flux.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Arabidopsis*
  • Gravitropism
  • Indoleacetic Acids
  • Membrane Transport Proteins
  • Phosphoric Monoester Hydrolases

Substances

  • Indoleacetic Acids
  • Membrane Transport Proteins
  • Phosphoric Monoester Hydrolases