Updated single cell reference atlas for the starlet anemone Nematostella vectensis

IF 2.6 2区 生物学 Q1 ZOOLOGY Frontiers in Zoology Pub Date : 2024-03-18 DOI:10.1186/s12983-024-00529-z
Alison G. Cole, Julia Steger, Julia Hagauer, Andreas Denner, Patricio Ferrer Murguia, Paul Knabl, Sanjay Narayanaswamy, Brittney Wick, Juan D. Montenegro, Ulrich Technau
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Abstract

The recent combination of genomics and single cell transcriptomics has allowed to assess a variety of non-conventional model organisms in much more depth. Single cell transcriptomes can uncover hidden cellular complexity and cell lineage relationships within organisms. The recent developmental cell atlases of the sea anemone Nematostella vectensis, a representative of the basally branching Cnidaria, has provided new insights into the development of all cell types (Steger et al Cell Rep 40(12):111370, 2022; Sebé-Pedrós et al. Cell 173(6):1520–1534.e20). However, the mapping of the single cell reads still suffers from relatively poor gene annotations and a draft genome consisting of many scaffolds. Here we present a new wildtype resource of the developmental single cell atlas, by re-mapping of sequence data first published in Steger et al. (2022) and Cole et al. (Nat Commun 14(1):1747, 2023), to the new chromosome-level genome assembly and corresponding gene models in Zimmermann et al. (Nat Commun 14, 8270 (2023). https://doi.org/10.1038/s41467-023-44080-7 ). We expand the pre-existing dataset through the incorporation of additional sequence data derived from the capture and sequencing of cell suspensions from four additional samples: 24 h gastrula, 2d planula, an inter-parietal region of the bodywall from a young unsexed animal, and another adult mesentery from a mature male animal. Our analyses of the full cell-state inventory provide transcriptomic signatures for 127 distinct cell states, of which 47 correspond to neuroglandular subtypes. We also identify two distinct putatively immune-related transcriptomic profiles that segregate between the inner and outer cell layers. Furthermore, the new gene annotation Nv2 has markedly improved the mapping on the single cell transcriptome data and will therefore be of great value for the community and anyone using the dataset.
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更新小海葵的单细胞参考图谱
最近,基因组学和单细胞转录组学的结合使我们能够更深入地评估各种非常规模式生物。单细胞转录组可以揭示生物体内隐藏的细胞复杂性和细胞系关系。海葵(Nematostella vectensis)是基底分支腔肠动物的代表,最近的海葵发育细胞图谱为所有细胞类型的发育提供了新的见解(Steger et al Cell Rep 40(12):111370, 2022; Sebé-Pedrós et al. Cell 173(6):1520-1534.e20)。然而,单细胞读数的图谱绘制仍然受到基因注释相对较差和由许多支架组成的基因组草案的影响。在此,我们将首次发表于 Steger 等人(2022 年)和 Cole 等人(Nat Commun 14(1):1747, 2023 年)的序列数据与 Zimmermann 等人(Nat Commun 14, 8270 (2023). https://doi.org/10.1038/s41467-023-44080-7 )的新染色体级基因组组装和相应基因模型进行重新映射,从而展示了发育单细胞图谱的新野生型资源。我们从另外四个样本的细胞悬浮液中采集并测序了额外的序列数据,从而扩展了已有的数据集:这四个样本分别是:24 小时的胃胚层、2d 刨层、来自幼年无性动物的体壁顶骨间区域以及来自成熟雄性动物的另一个成年肠系膜。我们对全部细胞状态清单的分析提供了 127 种不同细胞状态的转录组特征,其中 47 种对应于神经腺亚型。我们还发现了内层和外层细胞之间两个不同的、推测与免疫相关的转录组特征。此外,新的基因注释 Nv2 显著改善了单细胞转录组数据的映射,因此对社区和使用该数据集的任何人都具有重要价值。
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来源期刊
CiteScore
4.90
自引率
0.00%
发文量
29
审稿时长
>12 weeks
期刊介绍: Frontiers in Zoology is an open access, peer-reviewed online journal publishing high quality research articles and reviews on all aspects of animal life. As a biological discipline, zoology has one of the longest histories. Today it occasionally appears as though, due to the rapid expansion of life sciences, zoology has been replaced by more or less independent sub-disciplines amongst which exchange is often sparse. However, the recent advance of molecular methodology into "classical" fields of biology, and the development of theories that can explain phenomena on different levels of organisation, has led to a re-integration of zoological disciplines promoting a broader than usual approach to zoological questions. Zoology has re-emerged as an integrative discipline encompassing the most diverse aspects of animal life, from the level of the gene to the level of the ecosystem. Frontiers in Zoology is the first open access journal focusing on zoology as a whole. It aims to represent and re-unite the various disciplines that look at animal life from different perspectives and at providing the basis for a comprehensive understanding of zoological phenomena on all levels of analysis. Frontiers in Zoology provides a unique opportunity to publish high quality research and reviews on zoological issues that will be internationally accessible to any reader at no cost. The journal was initiated and is supported by the Deutsche Zoologische Gesellschaft, one of the largest national zoological societies with more than a century-long tradition in promoting high-level zoological research.
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