Ezran Camille, Liu Shixuan, Chang Stephen, Ming Jingsi, Guethlein Lisbeth A, Wang Michael F Z, Dehghannasiri Roozbeh, Olivieri Julia, Frank Hannah K, Tarashansky Alexander, Koh Winston, Jing Qiuyu, Botvinnik Olga, Antony Jane, Pisco Angela Oliveira, Karkanias Jim, Yang Can, Ferrell James E, Boyd Scott D, Parham Peter, Long Jonathan Z, Wang Bo, Salzman Julia, De Vlaminck Iwijn, Wu Angela Ruohao, Quake Stephen R, Krasnow Mark A
Department of Biochemistry, Stanford University School of Medicine, Stanford, CA, USA.
Howard Hughes Medical Institute, Stanford University School of Medicine, Stanford, CA, USA.
Nature. 2025 Aug;644(8075):185-196. doi: 10.1038/s41586-025-09114-8. Epub 2025 Jul 30.
Mouse lemurs (Microcebus spp.) are an emerging primate model organism, but their genetics, cellular and molecular biology remain largely unexplored. In an accompanying paper, we performed large-scale single-cell RNA sequencing of 27 organs from mouse lemurs. We identified more than 750 molecular cell types, characterized their transcriptomic profiles and provided insight into primate evolution of cell types. Here we use the generated atlas to characterize mouse lemur genes, physiology, disease and mutations. We uncover thousands of previously unidentified lemur genes and hundreds of thousands of new splice junctions including over 85,000 primate splice junctions missing in mice. We systematically explore the lemur immune system by comparing global expression profiles of key immune genes in health and disease, and by mapping immune cell development, trafficking and activation. We characterize primate-specific and lemur-specific physiology and disease, including molecular features of the immune program, lemur adipocytes and metastatic endometrial cancer that resembles the human malignancy. We present expression patterns of more than 400 primate genes missing in mice, many with similar expression patterns to humans and some implicated in human disease. Finally, we provide an experimental framework for reverse genetic analysis by identifying naturally occurring nonsense mutations in three primate immune genes missing in mice and by analysing their transcriptional phenotypes. This work establishes a foundation for molecular and genetic analyses of mouse lemurs and prioritizes primate genes, isoforms, physiology and disease for future study.
小鼠狐猴(Microcebus spp.)是一种新兴的灵长类模式生物,但其遗传学、细胞生物学和分子生物学在很大程度上仍未得到充分探索。在一篇配套论文中,我们对小鼠狐猴的27个器官进行了大规模单细胞RNA测序。我们鉴定出750多种分子细胞类型,描绘了它们的转录组图谱,并深入了解了细胞类型的灵长类进化。在这里,我们利用生成的图谱来表征小鼠狐猴的基因、生理学、疾病和突变。我们发现了数千个以前未鉴定的狐猴基因和数十万新的剪接连接,其中包括85000多个小鼠中缺失的灵长类剪接连接。我们通过比较健康和疾病状态下关键免疫基因的整体表达谱,以及绘制免疫细胞的发育、运输和激活过程,系统地探索了狐猴的免疫系统。我们表征了灵长类特异性和狐猴特异性的生理学和疾病,包括免疫程序、狐猴脂肪细胞和类似于人类恶性肿瘤的转移性子宫内膜癌的分子特征。我们展示了小鼠中缺失的400多个灵长类基因的表达模式,其中许多与人类的表达模式相似,有些还与人类疾病有关。最后,我们通过鉴定小鼠中缺失的三个灵长类免疫基因中的自然发生的无义突变,并分析它们转录表型,为反向遗传分析提供了一个实验框架。这项工作为小鼠狐猴的分子和遗传分析奠定了基础,并为未来研究确定了灵长类基因、异构体、生理学和疾病的优先顺序。