Laboratoire Reproduction et Développement des Plantes, Université de Lyon, ENS de Lyon, UCB Lyon 1, CNRS, INRAE, 69342 Lyon, France; Department of Molecular Genetics, Center for Research in Agricultural Genomics (CRAG), CSIC-IRTA-UAB-UB, Campus UAB, Bellaterra (Cerdanyola del Vallès), 08193 Barcelona, Spain.
Laboratoire Reproduction et Développement des Plantes, Université de Lyon, ENS de Lyon, UCB Lyon 1, CNRS, INRAE, 69342 Lyon, France.
Curr Biol. 2021 Jan 11;31(1):228-237.e10. doi: 10.1016/j.cub.2020.10.011. Epub 2020 Nov 5.
Plants are able to orient their growth according to gravity, which ultimately controls both shoot and root architecture. Gravitropism is a dynamic process whereby gravistimulation induces the asymmetric distribution of the plant hormone auxin, leading to asymmetric growth, organ bending, and subsequent reset of auxin distribution back to the original pre-gravistimulation situation. Differential auxin accumulation during the gravitropic response depends on the activity of polarly localized PIN-FORMED (PIN) auxin-efflux carriers. In particular, the timing of this dynamic response is regulated by PIN2, but the underlying molecular mechanisms are poorly understood. Here, we show that MEMBRANE ASSOCIATED KINASE REGULATOR2 (MAKR2) controls the pace of the root gravitropic response. We found that MAKR2 is required for the PIN2 asymmetry during gravitropism by acting as a negative regulator of the cell-surface signaling mediated by the receptor-like kinase TRANSMEMBRANE KINASE1 (TMK1). Furthermore, we show that the MAKR2 inhibitory effect on TMK1 signaling is antagonized by auxin itself, which triggers rapid MAKR2 membrane dissociation in a TMK1-dependent manner. Our findings suggest that the timing of the root gravitropic response is orchestrated by the reversible inhibition of the TMK1 signaling pathway at the cell surface.
植物能够根据重力来调整其生长方向,而重力最终控制着茎和根的结构。向重性是一个动态过程,其中重刺激诱导植物激素生长素的不对称分布,导致不对称生长、器官弯曲,以及随后生长素分布恢复到原始重刺激前的情况。在向重性反应过程中,生长素的差异积累取决于极性定位的 PIN 形成(PIN)生长素外排载体的活性。特别是,这种动态反应的时间由 PIN2 调节,但潜在的分子机制知之甚少。在这里,我们表明,膜相关激酶调节剂 2(MAKR2)通过作为受体样激酶 TRANSMEMBRANE KINASE1(TMK1)介导的细胞表面信号的负调节剂,控制根向重性反应的速度。我们发现 MAKR2 作为 TMK1 信号的负调节剂,在向重性过程中需要 PIN2 的不对称性。此外,我们表明,生长素本身拮抗 MAKR2 对 TMK1 信号的抑制作用,生长素以 TMK1 依赖的方式触发 MAKR2 膜的快速解离。我们的研究结果表明,根向重性反应的时间由细胞表面 TMK1 信号通路的可逆抑制来协调。