Starr Alexander L, Nishimura Toshiya, Igarashi Kyomi J, Funamoto Chihiro, Nakauchi Hiromitsu, Fraser Hunter B
Department of Biology, Stanford University, Stanford, CA 94305, USA.
Institute for Stem Cell Biology and Regenerative Medicine, Department of Genetics, Stanford University School of Medicine, Stanford, CA 94305, USA; Division of Stem Cell and Organoid Medicine, Department of Genome Biology, Graduate School of Medicine, Osaka University, Osaka 565-0871, Japan.
Cell Genom. 2025 May 24:100891. doi: 10.1016/j.xgen.2025.100891.
A long-standing question in biology is the extent to which cells function autonomously as opposed to requiring interactions with other cells or environmental factors. Here, we develop a framework to use interspecies chimeras to precisely decompose evolutionary divergence in any cellular trait into cell-intrinsic and cell-extrinsic components. Applying this framework to thousands of gene expression levels in reciprocal rat-mouse chimeras, we found that most divergence is cell intrinsic, though extrinsic factors also play an integral role. For example, cell-extrinsic regulation of a transcription factor can propagate to its target genes, leading to cell-type-specific extrinsic regulation of both their mRNA and their protein levels. We also show that imprinted genes are dramatically misexpressed in chimeras, suggesting a mismatch between rapidly evolving intrinsic and extrinsic imprinting mechanisms. Overall, our conceptual framework opens up new avenues to investigate the mechanistic basis of the evolution, development, and regulation of myriad cellular traits in any multicellular organism.
生物学中一个长期存在的问题是,细胞在多大程度上独立发挥功能,而不是需要与其他细胞或环境因素相互作用。在这里,我们开发了一个框架,利用种间嵌合体将任何细胞特征的进化差异精确分解为细胞内在和细胞外在成分。将这个框架应用于互惠大鼠-小鼠嵌合体中的数千个基因表达水平,我们发现大多数差异是细胞内在的,尽管外在因素也起着不可或缺的作用。例如,转录因子的细胞外调节可以传播到其靶基因,导致其mRNA和蛋白质水平的细胞类型特异性外在调节。我们还表明,印记基因在嵌合体中显著错误表达,这表明快速进化的内在和外在印记机制之间存在不匹配。总体而言,我们的概念框架为研究任何多细胞生物体中无数细胞特征的进化、发育和调节的机制基础开辟了新途径。