Single-cell atlas in the living fossil Yangtze sturgeon provides insight into the evolution of fish

IF 10.1 1区 生物学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Yeyu Chen, Xiaoyun Wu, Jiansheng Lai, Pengcheng Li, Ya Liu, Zhao Liu, Qiaolin Zou, Luyun Ni, Mingjiang Song, Feiyang Li, Quan Gong
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引用次数: 0

Abstract

Fish are the largest group of vertebrates. Studying the characteristics, functions, and interactions of different fish cells is important for understanding their roles in disease and evolution. However, most single cell RNA-seq studies in fish are restricted to a few specific organs, leaving a comprehensive cell landscape that aims to characterize the heterogeneity and connections among body-wide organs largely unexplored. We construct a single-cell atlas from the Yangtze sturgeon, Acipenser dabryanus, containing 82,401 high-quality cells and identify 72 major cell types. We compare differentially expressed genes among enterocytes in each part of the intestines and reveal the differences in absorption function of pyloric caecum, duodenum, spiral intestine, and rectum. Best4/Otop2 cells, newly identified in human, are also found in the intestines of sturgeon, indicating that these cells originated in an ancient period. We confirm the status of Müller glia as resident stem cells in fish nervous systems. We also characterize the different immune function between mucosa- and systemic-associated tissues. We detect several unexpected types of cells in Yangtze sturgeon, confirming that sturgeon is basal to teleosts. Cross-species analysis further indicates that sturgeon might occupy an ancient evolutionary position bridging the transition from cartilaginous to bony fish. In addition, novel cell markers, transcription factors, and intercellular communications are identified and found to be associated with the biological functions of specific types of cells. We generate the cellular landscape of an ancient fish and provide a valuable resource for revealing the cellular heterogeneity and biology of vertebrates.
活化石长江鲟的单细胞图谱为鱼类的进化提供了洞见
鱼是脊椎动物中最大的一类。研究不同鱼类细胞的特征、功能和相互作用对于了解它们在疾病和进化中的作用是重要的。然而,大多数鱼类单细胞RNA-seq研究仅限于少数特定器官,留下了一个全面的细胞景观,旨在表征全身器官之间的异质性和联系,在很大程度上未被探索。我们构建了扬子鲟(Acipenser dabryanus)的单细胞图谱,包含82,401个高质量细胞,鉴定出72种主要细胞类型。我们比较了肠道各部分肠细胞的差异表达基因,揭示了幽门盲肠、十二指肠、螺旋肠和直肠吸收功能的差异。在人类中新发现的Best4/Otop2细胞也在鲟鱼的肠道中发现,这表明这些细胞起源于一个古老的时期。我们证实了神经胶质细胞作为驻留干细胞在鱼类神经系统中的地位。我们还描述了粘膜和全身相关组织之间不同的免疫功能。我们在长江鲟身上发现了几种意想不到的细胞类型,证实了长江鲟是硬骨鱼的基础。跨物种分析进一步表明,鲟鱼可能占据了一个古老的进化位置,连接着从软骨鱼类到硬骨鱼类的过渡。此外,新的细胞标记物、转录因子和细胞间通讯被鉴定并发现与特定类型细胞的生物学功能相关。我们生成了古代鱼类的细胞景观,为揭示脊椎动物的细胞异质性和生物学提供了宝贵的资源。
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来源期刊
Genome Biology
Genome Biology Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
21.00
自引率
3.30%
发文量
241
审稿时长
2 months
期刊介绍: Genome Biology stands as a premier platform for exceptional research across all domains of biology and biomedicine, explored through a genomic and post-genomic lens. With an impressive impact factor of 12.3 (2022),* the journal secures its position as the 3rd-ranked research journal in the Genetics and Heredity category and the 2nd-ranked research journal in the Biotechnology and Applied Microbiology category by Thomson Reuters. Notably, Genome Biology holds the distinction of being the highest-ranked open-access journal in this category. Our dedicated team of highly trained in-house Editors collaborates closely with our esteemed Editorial Board of international experts, ensuring the journal remains on the forefront of scientific advances and community standards. Regular engagement with researchers at conferences and institute visits underscores our commitment to staying abreast of the latest developments in the field.
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