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使用3D细胞图谱对植物器官发育进行数字单细胞分析。

Digital Single-Cell Analysis of Plant Organ Development Using 3DCellAtlas.

作者信息

Montenegro-Johnson Thomas D, Stamm Petra, Strauss Soeren, Topham Alexander T, Tsagris Michail, Wood Andrew T A, Smith Richard S, Bassel George W

机构信息

School of Mathematics, University of Birmingham, Birmingham B15 2TT, United Kingdom.

School of Biosciences, University of Birmingham, Birmingham B15 2TT, United Kingdom.

出版信息

Plant Cell. 2015 Apr;27(4):1018-33. doi: 10.1105/tpc.15.00175. Epub 2015 Apr 21.

Abstract

Diverse molecular networks underlying plant growth and development are rapidly being uncovered. Integrating these data into the spatial and temporal context of dynamic organ growth remains a technical challenge. We developed 3DCellAtlas, an integrative computational pipeline that semiautomatically identifies cell types and quantifies both 3D cellular anisotropy and reporter abundance at single-cell resolution across whole plant organs. Cell identification is no less than 97.8% accurate and does not require transgenic lineage markers or reference atlases. Cell positions within organs are defined using an internal indexing system generating cellular level organ atlases where data from multiple samples can be integrated. Using this approach, we quantified the organ-wide cell-type-specific 3D cellular anisotropy driving Arabidopsis thaliana hypocotyl elongation. The impact ethylene has on hypocotyl 3D cell anisotropy identified the preferential growth of endodermis in response to this hormone. The spatiotemporal dynamics of the endogenous DELLA protein RGA, expansin gene EXPA3, and cell expansion was quantified within distinct cell types of Arabidopsis roots. A significant regulatory relationship between RGA, EXPA3, and growth was present in the epidermis and endodermis. The use of single-cell analyses of plant development enables the dynamics of diverse regulatory networks to be integrated with 3D organ growth.

摘要

植物生长和发育背后多样的分子网络正迅速被揭示。将这些数据整合到动态器官生长的时空背景中仍然是一项技术挑战。我们开发了3DCellAtlas,这是一种综合计算流程,可在全植物器官的单细胞分辨率下半自动识别细胞类型,并量化3D细胞各向异性和报告基因丰度。细胞识别准确率不低于97.8%,且不需要转基因谱系标记或参考图谱。器官内的细胞位置使用内部索引系统定义,生成细胞水平的器官图谱,可整合多个样本的数据。使用这种方法,我们量化了驱动拟南芥下胚轴伸长的全器官细胞类型特异性3D细胞各向异性。乙烯对下胚轴3D细胞各向异性的影响确定了内皮层对这种激素的优先生长反应。在内源DELLA蛋白RGA、扩展蛋白基因EXPA3和细胞扩张的时空动态在拟南芥根的不同细胞类型中进行了量化。RGA、EXPA3和生长之间存在显著的调节关系,存在于表皮和内皮层中。对植物发育进行单细胞分析能够将多样调控网络的动态与3D器官生长整合起来。

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