Zacharias Amanda L, Murray John Isaac
Department of Genetics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
Genesis. 2016 Apr;54(4):182-97. doi: 10.1002/dvg.22928. Epub 2016 Mar 19.
Understanding how a single cell, the zygote, can divide and differentiate to produce the diverse animal cell types is a central goal of developmental biology research. The model organism Caenorhabditis elegans provides a system that enables a truly comprehensive understanding of this process across all cells. Its invariant cell lineage makes it possible to identify all of the cells in each individual and compare them across organisms. Recently developed methods automate the process of cell identification, allowing high-throughput gene expression characterization and phenotyping at single cell resolution. In this Review, we summarize the sequences of events that pattern the lineage including establishment of founder cell identity, the signaling pathways that diversify embryonic fate, and the regulators involved in patterning within these founder lineages before cells adopt their terminal fates. We focus on insights that have emerged from automated approaches to lineage tracking, including insights into mechanisms of robustness, context-specific regulation of gene expression, and temporal coordination of differentiation. We suggest a model by which lineage history produces a combinatorial code of transcription factors that act, often redundantly, to ensure terminal fate.
理解单个细胞——受精卵——如何分裂和分化以产生多样的动物细胞类型,是发育生物学研究的核心目标。模式生物秀丽隐杆线虫提供了一个系统,能让人真正全面地了解这一贯穿所有细胞的过程。其不变的细胞谱系使得识别每个个体中的所有细胞并在不同生物体间进行比较成为可能。最近开发的方法实现了细胞识别过程的自动化,从而能够在单细胞分辨率下进行高通量基因表达特征分析和表型分析。在本综述中,我们总结了构建谱系的一系列事件,包括起始细胞身份的确立、使胚胎命运多样化的信号通路,以及在细胞进入终末命运之前参与这些起始谱系模式形成的调控因子。我们重点关注从谱系追踪的自动化方法中获得的见解,包括对稳健性机制、基因表达的上下文特异性调控以及分化的时间协调的见解。我们提出了一个模型,即谱系历史产生转录因子的组合密码,这些转录因子通常以冗余方式起作用,以确保终末命运。