Spatiotemporal transcriptomic atlas of mouse organogenesis using DNA nanoball-patterned arrays

Ao Chen(BGI Group (China)), Sha Liao(BGI Group (China)), Mengnan Cheng(BGI Group (China)), Kailong Ma(BGI Group (China)), Liang Wu(BGI Group (China)), Yiwei Lai(BGI Group (China)), Xiaojie Qiu(Howard Hughes Medical Institute), Jin Min Yang(BGI Group (China)), Jiangshan Xu(BGI Group (China)), Shijie Hao(BGI Group (China)), Xin Wang(BGI Group (China)), Huifang Lü(BGI Group (China)), Xi Chen(BGI Group (China)), Xing Liu(BGI Group (China)), Xin Huang(BGI Group (China)), Li Zhao(BGI Group (China)), Hong Yan(BGI Group (China)), Yujia Jiang(BGI Group (China)), Jian Peng(BGI Group (China)), Shuai Liu(BGI Group (China)), Mengzhe Shen(BGI Group (China)), Chuanyu Liu(BGI Group (China)), Quanshui Li(BGI Group (China)), Yue Yuan(BGI Group (China)), Xiaoyu Wei(BGI Group (China)), Huiwen Zheng(BGI Group (China)), Weimin Feng(BGI Group (China)), Zhifeng Wang(BGI Group (China)), Yang Liu(BGI Group (China)), Zhaohui Wang(BGI Group (China)), Yunzhi Yang(BGI Group (China)), Haitao Xiang(BGI Group (China)), Lei Han(BGI Group (China)), Baoming Qin(Chinese Academy of Sciences), Peng-Cheng Guo(Chinese Academy of Sciences), Guangyao Lai(Chinese Academy of Sciences), Pura Muñoz‐Cánoves(Institució Catalana de Recerca i Estudis Avançats), Patrick H. Maxwell(University of Cambridge), Jean Paul Thiery, Qingfeng Wu(Chinese Academy of Sciences), Fuxiang Zhao(BGI Group (China)), Bichao Chen(BGI Group (China)), Mei Li(BGI Group (China)), Xi Dai(BGI Group (China)), Shuai Wang(BGI Group (China)), Haoyan Kuang(BGI Group (China)), Junhou Hui(BGI Group (China)), Liqun Wang(Guangdong Academy of Medical Sciences), Ji‐Feng Fei(Guangdong Academy of Medical Sciences), Ou Wang(BGI Group (China)), Xiaofeng Wei(BGI Group (China)), Haorong Lu(BGI Group (China)), Bo Wang(China National GeneBank), Shiping Liu(BGI Group (China)), Ying Gu(BGI Group (China)), Ming Ni(BGI Group (China)), Wenwei Zhang(BGI Group (China)), Feng Mu(BGI Group (China)), Ye Yin(BGI Group (China)), Huanming Yang(BGI Group (China)), Michael Lisby(University of Copenhagen), Richard J. Cornall(University of Oxford), Jan Mulder(Science for Life Laboratory), Mathias Uhlén(Science for Life Laboratory), Miguel A. Esteban(BGI Group (China)), Yuxiang Li(BGI Group (China)), Longqi Liu(BGI Group (China)), Xun Xu(BGI Group (China)), Jian Wang(BGI Group (China))
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Abstract

Spatially resolved transcriptomic technologies are promising tools to study complex biological processes such as mammalian embryogenesis. However, the imbalance between resolution, gene capture, and field of view of current methodologies precludes their systematic application to analyze relatively large and three-dimensional mid- and late-gestation embryos. Here, we combined DNA nanoball (DNB)-patterned arrays and in situ RNA capture to create spatial enhanced resolution omics-sequencing (Stereo-seq). We applied Stereo-seq to generate the mouse organogenesis spatiotemporal transcriptomic atlas (MOSTA), which maps with single-cell resolution and high sensitivity the kinetics and directionality of transcriptional variation during mouse organogenesis. We used this information to gain insight into the molecular basis of spatial cell heterogeneity and cell fate specification in developing tissues such as the dorsal midbrain. Our panoramic atlas will facilitate in-depth investigation of longstanding questions concerning normal and abnormal mammalian development.


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