PRC2调控拟南芥细胞分裂素和HD-ZIP III通路,协调维管组织模式的形成。

Yufei Zhang,Runzhou Huang,Tingting Yang,An Li,Zihao Wang,Yuexin Wu,Yang Deng,Jing Zhang,Xin-Qiang He,Yue Zhou
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引用次数: 0

摘要

多梳抑制复合体2 (Polycomb suppressuppressicomplex 2, PRC2)调控植物发育,但系统性PRC2突变体具有多效性缺陷,这使其调控次生生长的研究复杂化。在这里,我们使用CRISPR-TSKO在拟南芥(Arabidopsis thaliana)中产生了维管组织特异性敲除PRC2成分受精独立胚乳(FIE),该成分由维管组织特异性基因WUSCHEL HOMEOBOX RELATED 14 (WOX14)的启动子驱动,称为WOX14pro:FIE- ko。WOX14pro: 5 - ko植物在韧皮部薄壁组织中表现出异位维管束和维管柱,木质部网状或凹陷维管束和纤维的分化受到抑制。RNA-seq和ChIP分析表明,FIE直接介导H3K27me3沉积在编码异戊烯基转移酶(IPT)细胞分裂素生物合成酶的基因上,抑制其转录,调节细胞分裂素在下胚轴的空间分布和反应。细胞分裂素生物合成或信号转导的遗传操作部分挽救了基因敲除的下胚轴的血管缺陷。此外,我们发现HOMEODOMAIN LEUCINE ZIPPER CLASS III (HD-ZIPIII)转录因子是5 - ipt模块的下游靶标,在WOX14pro:FIE/IPT3/IPT5/IPT7-KO中表达减少,而在WOX14pro:FIE/IPT3/IPT5/IPT7-KO中表达恢复。在WOX14pro:FIE-KO中过表达拟南芥同源box基因8 (ATHB8)也部分修复了血管缺陷。总的来说,我们的发现扩大了组织特异性敲除技术在植物中的应用,并建立了PRC2及其下游信号级联作为维管组织模式的调节剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
PRC2 regulates cytokinin and HD-ZIP III pathways to orchestrate vascular tissue pattern formation in Arabidopsis.
Polycomb repressive complex 2 (PRC2) regulates plant development, but systemic PRC2 mutants have pleiotropic defects that complicate investigation of its role in regulating secondary growth. Here, we used CRISPR-TSKO to generate a vascular tissue-specific knockout of the PRC2 component FERTILIZATION INDEPENDENT ENDOSPERM (FIE) driven by the promoter of the vascular tissue-specific gene WUSCHEL HOMEOBOX RELATED 14 (WOX14), termed WOX14pro:FIE-KO, in Arabidopsis (Arabidopsis thaliana). WOX14pro:FIE-KO plants showed ectopic vascular bundles, vascular cylinders within the phloem parenchyma, and inhibited differentiation of reticulate or pitted vessels and fibers in xylem. RNA-seq and ChIP analyses revealed that FIE directly mediates H3K27me3 deposition on genes encoding isopentenyltransferase (IPT) cytokinin biosynthesis enzymes, repressing their transcription and modulating cytokinin's spatial distribution and responses in hypocotyls. Genetic manipulation of cytokinin biosynthesis or signal transduction partially rescued vascular defects in FIE-knockout hypocotyls. Furthermore, we identified HOMEODOMAIN LEUCINE ZIPPER CLASS III (HD-ZIPIII) transcription factors as downstream targets of the FIE-IPT module, showing reduced expression in WOX14pro:FIE-KO and restoration in WOX14pro:FIE/IPT3/IPT5/IPT7-KO. Overexpression of ARABIDOPSIS HOMEOBOX GENE 8 (ATHB8) in WOX14pro:FIE-KO also partially rescued the vascular defects. Collectively, our findings expand the application of tissue-specific knockout technology in plants and establish PRC2 and its downstream signaling cascade as regulators of vascular tissue patterning.
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