Department of Biology and Zurich-Basel Plant Science Center, Swiss Federal Institute of Technology, ETH Centre, CH-8092 Zurich, Switzerland.
Plant Cell. 2011 Mar;23(3):1047-60. doi: 10.1105/tpc.111.083352. Epub 2011 Mar 25.
The chromatin modifying Polycomb group (PcG) and trithorax group (trxG) proteins are central regulators of cell identity that maintain a tightly controlled balance between cell proliferation and cell differentiation. The opposing activities of PcG and trxG proteins ensure the correct expression of specific transcriptional programs at defined developmental stages. Here, we report that the chromatin remodeling factor PICKLE (PKL) and the PcG protein CURLY LEAF (CLF) antagonistically determine root meristem activity. Whereas loss of PKL function caused a decrease in meristematic activity, loss of CLF function increased meristematic activity. Alterations of meristematic activity in pkl and clf mutants were not connected with changes in auxin concentration but correlated with decreased or increased expression of root stem cell and meristem marker genes, respectively. Root stem cell and meristem marker genes are modified by the PcG-mediated trimethylation of histone H3 on lysine 27 (H3K27me3). Decreased expression levels of root stem cell and meristem marker genes in pkl correlated with increased levels of H3K27me3, indicating that root meristem activity is largely controlled by the antagonistic activity of PcG proteins and PKL.
染色质修饰的多梳组 (PcG) 和三翼旋转木马组 (trxG) 蛋白是细胞身份的核心调节剂,它们在细胞增殖和细胞分化之间保持着严格的平衡。PcG 和 trxG 蛋白的拮抗活性确保了特定转录程序在特定发育阶段的正确表达。在这里,我们报告说染色质重塑因子 PICKLE (PKL) 和 PcG 蛋白 CURLY LEAF (CLF) 拮抗地决定根分生组织的活性。虽然 PKL 功能丧失导致分生组织活性降低,但 CLF 功能丧失增加了分生组织的活性。pkl 和 clf 突变体中分生组织活性的改变与生长素浓度的变化无关,而是分别与根干细胞和分生组织标记基因的表达减少或增加相关。根干细胞和分生组织标记基因被 PcG 介导的组蛋白 H3 赖氨酸 27 三甲基化 (H3K27me3) 修饰。pkl 中根干细胞和分生组织标记基因表达水平的降低与 H3K27me3 水平的升高相关,表明根分生组织的活性主要受 PcG 蛋白和 PKL 的拮抗活性控制。