神经发生
核糖核酸
生物
RNA序列
转录组
核心
基因表达
海马结构
细胞
神经科学
基因
电池类型
海马体
计算生物学
遗传学
作者
Naomi Habib,Yinqing Li,Matthias Heidenreich,Lukasz Swiech,Inbal Avraham‐Davidi,John J. Trombetta,Cynthia C. Hession,Feng Zhang,Aviv Regev
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2016-07-29
卷期号:353 (6302): 925-928
被引量:550
标识
DOI:10.1126/science.aad7038
摘要
Single-cell RNA sequencing (RNA-Seq) provides rich information about cell types and states. However, it is difficult to capture rare dynamic processes, such as adult neurogenesis, because isolation of rare neurons from adult tissue is challenging and markers for each phase are limited. Here, we develop Div-Seq, which combines scalable single-nucleus RNA-Seq (sNuc-Seq) with pulse labeling of proliferating cells by 5-ethynyl-2'-deoxyuridine (EdU) to profile individual dividing cells. sNuc-Seq and Div-Seq can sensitively identify closely related hippocampal cell types and track transcriptional dynamics of newborn neurons within the adult hippocampal neurogenic niche, respectively. We also apply Div-Seq to identify and profile rare newborn neurons in the adult spinal cord, a noncanonical neurogenic region. sNuc-Seq and Div-Seq open the way for unbiased analysis of diverse complex tissues.
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