Tom Denyer, Pin-Jou Wu, Kelly Colt, Bradley W Abramson, Zhili Pang, Pavel Solansky, Allen Mamerto, Tatsuya Nobori, Joseph R Ecker, Eric Lam, Todd P Michael, Marja C P Timmermans
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引用次数: 0
摘要
单细胞基因组学为分子和细胞动态研究提供了新的分辨率,可以对细胞类型和细胞在发育过程中的行为以及对环境条件(如与水的相互作用和地球的光-暗循环)的反应进行全面、平行的评估。在这里,我们利用半水生的澳大利亚狼尾草(Wolffia australiana)这种最小、也可能是结构最简单的植物,来了解这些情况下细胞在整株植物水平上的表达动态。我们研究了单细胞分辨率的 RNA 测序数据,发现灰灰菜细胞分为四个主要群组,分别代表水上和水下的实质和表皮。虽然这些组织与模式植物的转录组相似,但它们显示了狼尾草对水生环境的独特适应性。在这一广泛的分类中,离散的亚专业化非常明显,部分细胞显示出与发育成熟和专业生理相关的独特转录组特征。通过在两个关键的日时(TOD)转换阶段对这一简化的生物系统进行时间评估,我们发现了更多以前在全植物转录组学方法中被忽视的 TOD 响应基因,并证明即使在这一简化系统中,核心昼夜节律时钟机制及其下游响应也会以细胞特异性的方式发生变化。细胞类型之间的差异及其对浸没和/或 TOD 的反应是由出乎意料的少数基因的表达变化驱动的,这说明狼尾草是一种高度精简的生物体,其大部分基因都用于基本的细胞过程。狼尾草为应用还原生物学阐明生物体水平的信号功能提供了一个独特的机会,这项工作为此提供了强大的资源。
Streamlined spatial and environmental expression signatures characterize the minimalist duckweed Wolffia australiana.
Single-cell genomics permits a new resolution in the examination of molecular and cellular dynamics, allowing global, parallel assessments of cell types and cellular behaviors through development and in response to environmental circumstances, such as interaction with water and the light-dark cycle of the Earth. Here, we leverage the smallest, and possibly most structurally reduced, plant, the semiaquatic Wolffia australiana, to understand dynamics of cell expression in these contexts at the whole-plant level. We examined single-cell-resolution RNA-sequencing data and found Wolffia cells divide into four principal clusters representing the above- and below-water-situated parenchyma and epidermis. Although these tissues share transcriptomic similarity with model plants, they display distinct adaptations that Wolffia has made for the aquatic environment. Within this broad classification, discrete subspecializations are evident, with select cells showing unique transcriptomic signatures associated with developmental maturation and specialized physiologies. Assessing this simplified biological system temporally at two key time-of-day (TOD) transitions, we identify additional TOD-responsive genes previously overlooked in whole-plant transcriptomic approaches and demonstrate that the core circadian clock machinery and its downstream responses can vary in cell-specific manners, even in this simplified system. Distinctions between cell types and their responses to submergence and/or TOD are driven by expression changes of unexpectedly few genes, characterizing Wolffia as a highly streamlined organism with the majority of genes dedicated to fundamental cellular processes. Wolffia provides a unique opportunity to apply reductionist biology to elucidate signaling functions at the organismal level, for which this work provides a powerful resource.
期刊介绍:
Launched in 1995, Genome Research is an international, continuously published, peer-reviewed journal that focuses on research that provides novel insights into the genome biology of all organisms, including advances in genomic medicine.
Among the topics considered by the journal are genome structure and function, comparative genomics, molecular evolution, genome-scale quantitative and population genetics, proteomics, epigenomics, and systems biology. The journal also features exciting gene discoveries and reports of cutting-edge computational biology and high-throughput methodologies.
New data in these areas are published as research papers, or methods and resource reports that provide novel information on technologies or tools that will be of interest to a broad readership. Complete data sets are presented electronically on the journal''s web site where appropriate. The journal also provides Reviews, Perspectives, and Insight/Outlook articles, which present commentary on the latest advances published both here and elsewhere, placing such progress in its broader biological context.