Short-read and long-read full-length transcriptome of mouse neural stem cells across neurodevelopmental stages

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作者
Chaoqiong Ding
Xiang Yan
Mengying Xu
Ran Zhou
Yuancun Zhao
Dan Zhang
Zongyao Huang
Zhenzhong Pan
Peng Xiao
Huifang Li
Lu Chen
Yuan Wang
机构
[1] Sichuan University and National Collaborative Innovation Center,Department of Neurosurgery, State Key Laboratory of Biotherapy and Cancer Center, West China Hospital
[2] Sichuan University,Key Laboratory of Birth Defects and Related Diseases of Women and Children of MOE, State Key Laboratory of Biotherapy, West China Second Hospital
[3] Sichuan University,Core Facilities of West China Hospital
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During brain development, neural stem cells (NSCs) undergo multiple fate-switches to generate various neuronal subtypes and glial cells, exhibiting distinct transcriptomic profiles at different stages. However, full-length transcriptomic datasets of NSCs across different neurodevelopmental stages under similar experimental settings are lacking, which is essential for uncovering stage-specific transcriptional and post-transcriptional mechanisms underlying the fate commitment of NSCs. Here, we report the full-length transcriptome of mouse NSCs at five different stages during embryonic and postnatal development. We used fluorescent-activated cell sorting (FACS) to isolate CD133+Blbp+ NSCs from C57BL/6 transgenic mice that express enhanced green fluorescent protein (EGFP) under the control of a Blbp promoter. By integrating short- and long-read full-length RNA-seq, we created a transcriptomic dataset of gene and isoform expression profiles in NSCs at embryonic days 15.5, 17.5, and postnatal days 1.5, 8, and 60. This dataset provides a detailed characterization of full-length transcripts in NSCs at distinct developmental stages, which could be used as a resource for the neuroscience community to study NSC fate determination, neural development, and disease.
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