Center for Soft and Living Matter, Institute for Basic Science (IBS), Ulsan, 44919, South Korea.
Department of Physics, Ulsan National Institute of Science and Technology (UNIST), Ulsan, 44919, South Korea.
BMC Biol. 2021 May 21;19(1):111. doi: 10.1186/s12915-021-01013-4.
Multicellular organisms are characterized by a wide diversity of forms and complexity despite a restricted set of key molecules and mechanisms at the base of organismal development. Development combines three basic processes-asymmetric cell division, signaling, and gene regulation-in a multitude of ways to create this overwhelming diversity of multicellular life forms. Here, we use a generative model to test the limits to which such processes can be combined to generate multiple differentiation paths during development, and attempt to chart the diversity of multicellular organisms generated.
We sample millions of biologically feasible developmental schemes, allowing us to comment on the statistical properties of cell differentiation trajectories they produce. We characterize model-generated "organisms" using the graph topology of their cell type lineage maps. Remarkably, tree-type lineage differentiation maps are the rarest in our data. Additionally, a majority of the "organisms" generated by our model appear to be endowed with the ability to regenerate using pluripotent cells.
Our results indicate that, in contrast to common views, cell type lineage graphs are unlikely to be tree-like. Instead, they are more likely to be directed acyclic graphs, with multiple lineages converging on the same terminal cell type. Furthermore, the high incidence of pluripotent cells in model-generated organisms stands in line with the long-standing hypothesis that whole body regeneration is an epiphenomenon of development. We discuss experimentally testable predictions of our model and some ways to adapt the generative framework to test additional hypotheses about general features of development.
尽管生物体发育的基础是有限的关键分子和机制,但多细胞生物具有广泛的形态多样性和复杂性。发育将不对称细胞分裂、信号转导和基因调控这三个基本过程以多种方式结合起来,从而创造出多细胞生命形式的巨大多样性。在这里,我们使用生成模型来测试这些过程在多大程度上可以结合起来,以在发育过程中产生多种分化途径,并尝试绘制出所产生的多细胞生物的多样性图谱。
我们对数百万种具有生物学可行性的发育方案进行了采样,使我们能够对它们产生的细胞分化轨迹的统计特性进行评论。我们使用细胞类型谱系图的图拓扑结构来描述模型生成的“生物体”。值得注意的是,树状谱系分化图在我们的数据中是最罕见的。此外,我们模型生成的“生物体”大多数似乎都具有使用多能细胞进行再生的能力。
我们的结果表明,与常见观点相反,细胞类型谱系图不太可能是树状的。相反,它们更可能是有向无环图,多个谱系汇聚到相同的终末细胞类型。此外,模型生成的生物体中多能细胞的高发生率与长期以来的假设一致,即全身再生是发育的一种副现象。我们讨论了我们模型的可实验验证的预测,并提出了一些方法来调整生成框架,以测试关于发育一般特征的其他假设。