转录组
生物
核糖核酸
计算生物学
核心
RNA序列
原生质体
细胞生物学
基因
遗传学
基因表达
作者
Xin Xu,Fei Du,Yuling Jiao
出处
期刊:Methods in molecular biology
日期:2023-01-01
卷期号:: 307-311
标识
DOI:10.1007/978-1-0716-3299-4_15
摘要
Transcriptome profiling has been significantly hampered by the heterogeneity among individual cells within a tissue or an organ. Recent advances in single cell transcriptome profiling have significantly advanced our understanding of the transcriptome. However, plant single-cell RNA sequencing (scRNA-seq) relies on the isolation of protoplasts, which is not only impossible for many cell types but also induces acute wounding responses. To solve these problems, single-nucleus RNA sequencing (snRNA-seq) has been applied to plant research, in which nuclei are isolated and subject to encapsulation and profiling. Compared with scRNA-seq, snRNA-seq can be applied to a wider range of tissue types and plant species. Nevertheless, fewer transcripts can be obtained from each nucleus than each protoplast. In this chapter, we describe a detailed and general protocol to prepare nuclei from plant tissues that are ready for subsequent library construction and high-throughput sequencing.
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