Section of Genetic Medicine, Department of Medicine, University of Chicago, Chicago, Illinois, United States of America.
Department of Human Genetics, University of Chicago, Chicago, Illinois, United States of America.
PLoS Genet. 2022 Mar 9;18(3):e1010073. doi: 10.1371/journal.pgen.1010073. eCollection 2022 Mar.
The evolution of complex skeletal traits in primates was likely influenced by both genetic and environmental factors. Because skeletal tissues are notoriously challenging to study using functional genomic approaches, they remain poorly characterized even in humans, let alone across multiple species. The challenges involved in obtaining functional genomic data from the skeleton, combined with the difficulty of obtaining such tissues from nonhuman apes, motivated us to consider an alternative in vitro system with which to comparatively study gene regulation in skeletal cell types. Specifically, we differentiated six human (Homo sapiens) and six chimpanzee (Pan troglodytes) induced pluripotent stem cell lines (iPSCs) into mesenchymal stem cells (MSCs) and subsequently into osteogenic cells (bone cells). We validated differentiation using standard methods and collected single-cell RNA sequencing data from over 100,000 cells across multiple samples and replicates at each stage of differentiation. While most genes that we examined display conserved patterns of expression across species, hundreds of genes are differentially expressed (DE) between humans and chimpanzees within and across stages of osteogenic differentiation. Some of these interspecific DE genes show functional enrichments relevant in skeletal tissue trait development. Moreover, topic modeling indicates that interspecific gene programs become more pronounced as cells mature. Overall, we propose that this in vitro model can be used to identify interspecific regulatory differences that may have contributed to skeletal trait differences between species.
灵长类动物复杂骨骼特征的进化可能受到遗传和环境因素的影响。由于骨骼组织是功能基因组学研究中众所周知的具有挑战性的组织,即使在人类中,它们的特征也描述得很差,更不用说在多个物种中了。从骨骼中获取功能基因组数据所涉及的挑战,加上从非人类猿类中获取这些组织的困难,促使我们考虑使用替代的体外系统来比较研究骨骼细胞类型中的基因调控。具体来说,我们将六个人类(智人)和六只黑猩猩(Pan troglodytes)诱导多能干细胞系(iPSC)分化为间充质干细胞(MSC),然后再分化为成骨细胞(骨细胞)。我们使用标准方法验证了分化,并在每个分化阶段的多个样本和重复中收集了超过 100,000 个细胞的单细胞 RNA 测序数据。虽然我们研究的大多数基因在物种间显示出保守的表达模式,但在人类和黑猩猩之间,有数百个基因在成骨分化的内部和跨阶段表现出差异表达(DE)。这些种间差异表达基因中的一些具有与骨骼组织特征发育相关的功能富集。此外,主题建模表明,随着细胞成熟,种间基因程序变得更加明显。总的来说,我们提出这种体外模型可用于鉴定可能导致物种间骨骼特征差异的种间调控差异。