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首页> 外文期刊>Plant and cell physiology >Auxin-Responsive (Phospho)proteome Analysis Reveals Key Biological Processes and Signaling Associated with Shoot-Borne Crown Root Development in Rice
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Auxin-Responsive (Phospho)proteome Analysis Reveals Key Biological Processes and Signaling Associated with Shoot-Borne Crown Root Development in Rice

机译:生长素响应(磷酸化)蛋白质组分析揭示了与水稻芽源性冠根发育相关的关键生物学过程和信号传导

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The rice root system is primarily composed of shoot-borne adventitious/crown roots (ARs/CRs) that develop from the coleoptile base, and therefore, it is an excellent model system for studying shoot-to-root trans-differentiation process. We reveal global changes in protein and metabolite abundance and protein phosphorylation in response to an auxin stimulus during CR development. The liquid chromatography-tandem mass spectrometry (LC-MS/MS) and gas chromatography-mass spectrometry (GC-MS) analyses of developing crown root primordia (CRP) and emerged CRs identified 334 proteins and 12 amino acids, respectively, that were differentially regulated upon auxin treatment. Gene ontology enrichment analysis of global proteome data uncovered the biological processes associated with chromatin conformational change, gene expression and cell cycle that were regulated by auxin signaling. Spatial gene expression pattern analysis of differentially abundant proteins disclosed their stage-specific dynamic expression pattern during CRP development. Further, our tempo-spatial gene expression and functional analyses revealed that auxin creates a regulatory module during CRP development and activates ethylene biosynthesis exclusively during CRP initiation. Further, the phosphoproteome analysis identified 8,220 phosphosites, which could be mapped to 1,594 phosphoproteins and of which 66 phosphosites were differentially phosphorylated upon auxin treatment. Importantly, we observed differential phosphorylation of the cyclin-dependent kinase G-2 (OsCDKG;2) and cell wall proteins, in response to auxin signaling, suggesting that auxin-dependent phosphorylation may be required for cell cycle activation and cell wall synthesis during root organogenesis. Thus, our study provides evidence for the translational and post-translational regulation during CR development downstream of the auxin signaling pathway.
机译:水稻根系主要由芽鞘基部发育而来的芽源不定根/冠根(ARs/CRs)组成,是研究芽根间反分化过程的优秀模型系统。我们揭示了 CR 发育过程中蛋白质和代谢物丰度以及蛋白质磷酸化响应生长素刺激的全局变化。液相色谱-串联质谱(LC-MS/MS)和气相色谱-质谱(GC-MS)分析的树冠根原基(CRP)和新兴CRs分别鉴定出334种蛋白质和12种氨基酸,这些蛋白质和氨基酸在生长素处理后受到差异调控。对全球蛋白质组数据进行基因本体富集分析,揭示了与染色质构象变化、基因表达和细胞周期相关的生物学过程,这些过程受生长素信号转导调控。差异丰度蛋白的空间基因表达模式分析揭示了其在CRP发展过程中的阶段特异性动态表达模式。此外,我们的时空基因表达和功能分析表明,生长素在 CRP 发育过程中产生调节模块,并在 CRP 启动期间仅激活乙烯生物合成。此外,磷酸化蛋白质组分析鉴定了 8,220 个磷酸化位点,可定位到 1,594 个磷蛋白,其中 66 个磷酸化位点在生长素处理后被差异磷酸化。重要的是,我们观察到细胞周期蛋白依赖性激酶 G-2 (OsCDKG;2)和细胞壁蛋白,响应生长素信号传导,表明生长素依赖性磷酸化可能是根器官发生过程中细胞周期激活和细胞壁合成所必需的。因此,我们的研究为生长素信号通路下游 CR 发育过程中的翻译和翻译后调控提供了证据。

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