| Literature DB >> 27160914 |
Junxiang Li1, Haofei Luo2, Rui Wang1, Jidong Lang3, Siyu Zhu2, Zhenming Zhang1, Jianhuo Fang3, Keke Qu1, Yuting Lin3, Haizhou Long4, Yi Yao4, Geng Tian3, Qiong Wu5.
Abstract
The growth plate (GP) comprising sequentially differentiated cell layers is a critical structure for bone elongation and regeneration. Although several key regulators in GP development have been identified using genetic perturbation, systematic understanding is still limited. Here, we used single-cell RNA-sequencing (RNA-seq) to determine the gene expression profiles of 217 single cells from GPs and developed a bioinformatics pipeline named Sinova to de novo reconstruct physiological GP development in both temporal and spatial high resolution. Our unsupervised model not only confirmed prior knowledge, but also enabled the systematic discovery of genes, potential signal pathways, and surface markers CD9/CD200 to precisely depict development. Sinova further identified the effective combination of transcriptional factors (TFs) that regulates GP maturation, and the result was validated using an in vitro EGFP-Col10a screening system. Our case systematically reconstructed molecular cascades in GP development through single-cell profiling, and the bioinformatics pipeline is applicable to other developmental processes. VIDEO ABSTRACT.Entities:
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Year: 2016 PMID: 27160914 DOI: 10.1016/j.celrep.2016.04.043
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423