BIN2-mediated phosphorylation of KAN1 integrates brassinosteroid and auxin signaling during poplar secondary growth

Wenrong Tan, Xiaolan Yue, Yangzhou Pan, Jin Hu, Rong Huang, Haili Tan, Feiyan Lan, Fei Yang, Hongbin Wei, Lucas Gutiérrez Rodríguez, Víctor Resco de Dios, Keming Luo, Yinan Yao
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Abstract

The spatial arrangement of phloem, cambium and xylem is crucial for secondary growth in tree species. During secondary growth, cambium cells produce secondary xylem inwards and secondary phloem outwards. While phytohormone regulators and differentiation mediators coordinate vascular development, their signaling crosstalk remains poorly understood. Here, we reveal that in poplar (Populus tomentosa), the GSK3 kinase BRASSINOSTEROID INSENSITIVE 2.1 (PtoBIN2.1), integrates brassinosteroid (BR) and auxin signaling during secondary growth by phosphorylating the transcription factor KANADI1 (KAN1), which functions as abaxial determinant. In the phloem/abaxial side, BIN2-mediated phosphorylation stabilizes KAN1, enhancing its suppression of auxin biosynthesis/signaling and HD-ZIP III adaxial determinants, thereby promoting phloem development while inhibiting cambial activity and xylem differentiation. Conversely, BR and auxin synergistically promote xylem formation, with auxin signaling being required for BR-mediated secondary growth. BRs or lower BIN2.1 levels decrease KAN1 stability through diminished phosphorylation, attenuating KAN1-driven inhibition of auxin signaling and consequently enhancing cambial proliferation and xylem development. Our findings establish a BIN2–KAN1 regulatory module that orchestrates phloem–xylem patterning and demonstrate how poplar integrates BR and auxin signaling to control secondary growth.
在杨树次生生长过程中,bin2介导的KAN1磷酸化整合了油菜素内酯和生长素信号
韧皮部、形成层和木质部的空间排列对树木次生生长至关重要。在次生生长过程中,形成层细胞向内产生次生木质部,向外产生次生韧皮部。虽然植物激素调节因子和分化介质协调维管发育,但它们之间的信号串扰仍然知之甚少。在这里,我们发现在杨树(Populus tomentosa)中,GSK3激酶brassinosteroids INSENSITIVE 2.1 (PtoBIN2.1)在次生生长过程中通过磷酸化转录因子KANADI1 (KAN1)整合brassinosteroids (BR)和生长素信号。在韧皮部/背面,bin2介导的磷酸化稳定了KAN1,增强了其对生长素生物合成/信号传导和HD-ZIP III正面决定因素的抑制,从而促进韧皮部发育,抑制形成层活性和木质部分化。相反,BR和生长素协同促进木质部形成,生长素信号是BR介导的次生生长所必需的。BRs或较低的BIN2.1水平通过磷酸化减少,减弱KAN1驱动的生长素信号抑制,从而增强形成层增殖和木质部发育,从而降低KAN1的稳定性。我们的研究结果建立了一个协调韧皮部-木质部模式的BIN2-KAN1调控模块,并展示了杨树如何整合BR和生长素信号来控制次生生长。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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