State Key Laboratory of Tree Genetics and Breeding, Chinese Academy of Forestry, Beijing 100091, China.
State Key Laboratory of Tree Genetics and Breeding, Northeast Forestry University, Harbin 150040, China.
Plant Cell. 2024 May 1;36(5):1806-1828. doi: 10.1093/plcell/koae040.
Wood formation involves consecutive developmental steps, including cell division of vascular cambium, xylem cell expansion, secondary cell wall (SCW) deposition, and programmed cell death. In this study, we identified PagMYB31 as a coordinator regulating these processes in Populus alba × Populus glandulosa and built a PagMYB31-mediated transcriptional regulatory network. PagMYB31 mutation caused fewer layers of cambial cells, larger fusiform initials, ray initials, vessels, fiber and ray cells, and enhanced xylem cell SCW thickening, showing that PagMYB31 positively regulates cambial cell proliferation and negatively regulates xylem cell expansion and SCW biosynthesis. PagMYB31 repressed xylem cell expansion and SCW thickening through directly inhibiting wall-modifying enzyme genes and the transcription factor genes that activate the whole SCW biosynthetic program, respectively. In cambium, PagMYB31 could promote cambial activity through TRACHEARY ELEMENT DIFFERENTIATION INHIBITORY FACTOR (TDIF)/PHLOEM INTERCALATED WITH XYLEM (PXY) signaling by directly regulating CLAVATA3/ESR-RELATED (CLE) genes, and it could also directly activate WUSCHEL HOMEOBOX RELATED4 (PagWOX4), forming a feedforward regulation. We also observed that PagMYB31 could either promote cell proliferation through the MYB31-MYB72-WOX4 module or inhibit cambial activity through the MYB31-MYB72-VASCULAR CAMBIUM-RELATED MADS2 (VCM2)/PIN-FORMED5 (PIN5) modules, suggesting its role in maintaining the homeostasis of vascular cambium. PagMYB31 could be a potential target to manipulate different developmental stages of wood formation.
木质部形成涉及连续的发育步骤,包括维管形成层的细胞分裂、木质部细胞的扩展、次生细胞壁(SCW)的沉积和程序性细胞死亡。在这项研究中,我们鉴定了 PagMYB31 作为一个协调因子,调节白杨 × 腺柳中的这些过程,并构建了 PagMYB31 介导的转录调控网络。PagMYB31 突变导致形成层细胞层数减少,纺锤形原始细胞、射线原始细胞、导管、纤维和射线细胞增大,木质部细胞 SCW 增厚增强,表明 PagMYB31 正向调节形成层细胞的增殖,负向调节木质部细胞的扩展和 SCW 的生物合成。PagMYB31 通过直接抑制细胞壁修饰酶基因和激活整个 SCW 生物合成程序的转录因子基因,分别抑制木质部细胞的扩展和 SCW 增厚。在形成层中,PagMYB31 可以通过直接调节 CLAVATA3/ESR-RELATED (CLE) 基因,通过 TRACHEARY ELEMENT DIFFERENTIATION INHIBITORY FACTOR (TDIF)/PHLOEM INTERCALATED WITH XYLEM (PXY) 信号促进形成层活性,还可以直接激活 WUSCHEL HOMEOBOX RELATED4 (PagWOX4),形成前馈调节。我们还观察到 PagMYB31 可以通过 MYB31-MYB72-WOX4 模块促进细胞增殖,也可以通过 MYB31-MYB72-VASCULAR CAMBIUM-RELATED MADS2 (VCM2)/PIN-FORMED5 (PIN5) 模块抑制形成层活性,表明其在维持维管形成层的稳态中发挥作用。PagMYB31 可能是操纵木质部形成不同发育阶段的潜在靶标。