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Volume 50 Issue 9
Sep.  2023
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Article Contents

Single-cell RNA-Seq reveals transcriptional regulatory networks directing the development of mouse maxillary prominence

doi: 10.1016/j.jgg.2023.02.008
Funds:

31970585, 32170544, and 31801056 to Q.B.), the National Key Research and Development Program of China (2017YFC1001800 to X.W.

The authors thank the Flow Cytometry Lab and Bioimaging Facility at Shanghai Institute of Precision Medicine for help with experiments and Wu Zuo for the help with data processing. This work was supported by the National Natural Science Foundation of China (82071096 to X.W

2018YFC1004703 to Q.B), the Fundamental research program funding of Ninth People's Hospital affiliated to Shanghai Jiao Tong University School of Medicine (JYZZ179 to J.S.), the Innovative research team of high-level local universities in Shanghai (SHSMU-ZLCX20211700), and the SHIPM-pi fund No. JY201803 from Shanghai Institute of Precision Medicine, Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine.

  • Received Date: 2022-10-10
  • Revised Date: 2023-01-15
  • Accepted Date: 2023-02-08
  • Publish Date: 2023-02-24
  • During vertebrate embryonic development, neural crest-derived ectomesenchyme within the maxillary prominences undergoes precisely coordinated proliferation and differentiation to give rise to diverse craniofacial structures, such as tooth and palate. However, the transcriptional regulatory networks underpinning such an intricate process have not been fully elucidated. Here, we perform single-cell RNA-Seq to comprehensively characterize the transcriptional dynamics during mouse maxillary development from embryonic day (E) 10.5–E14.5. Our single-cell transcriptome atlas of ~28,000 cells uncovers mesenchymal cell populations representing distinct differentiating states and reveals their developmental trajectory, suggesting that the segregation of dental from the palatal mesenchyme occurs at E11.5. Moreover, we identify a series of key transcription factors (TFs) associated with mesenchymal fate transitions and deduce the gene regulatory networks directed by these TFs. Collectively, our study provides important resources and insights for achieving a systems-level understanding of craniofacial morphogenesis and abnormality.
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