Pressl Christina, Baffuto Matthew, Darnell Paul, Wang Cuidong, Carroll Thomas S, Heintz Nathaniel, Mätlik Kert
Laboratory of Molecular Biology, The Rockefeller University, New York, New York, USA.
Bioinformatics Resource Center, The Rockefeller University, New York, New York, USA.
Curr Protoc. 2024 Dec;4(12):e70067. doi: 10.1002/cpz1.70067.
Most pathological conditions of the central nervous system do not affect all cell types to the same extent. Delineation of molecular events underlying disease symptoms, including genetic, epigenetic, and transcriptional changes, thus relies on the ability to characterize a specific cell type separately from others. We have developed a methodology for the collection of nuclear RNA and genomic DNA of specific cell types from frozen post-mortem striatum and cerebral cortex. This allows deep transcriptomic profiling of specific cell populations and characterization of their genomes and epigenetic properties. The method is based on the purification of cell nuclei, followed by fluorescence-activated sorting of nuclei (FANS) labeled with nucleic acid probes or antibodies binding to targets present in specific cell types. The protocol describes in detail the procedure for isolating and labeling neuronal and glial nuclei from human brain tissue, the steps that can be taken to extract RNA and genomic DNA, a way to combine the procedure with ATAC-seq to yield information about chromatin accessibility, as well as computational measures for assessing the quality of cell type-specific RNA-seq and ATAC-seq datasets. © 2024 The Author(s). Current Protocols published by Wiley Periodicals LLC. Basic Protocol 1: Tissue homogenization, isolation of cell nuclei by ultracentrifugation and formaldehyde-fixation Basic Protocol 2: Antibody-based labeling and isolation of nuclei of specific neocortical neuron types Support Protocol 1: Generation of ATAC-seq libraries from the nuclei of specific neuron types of the cerebral cortex Basic Protocol 3: Nucleic acid hybridization-based labeling and isolation of nuclei of specific striatal projection neuron types Alternate Protocol 1: Labeling and isolation of nuclei of specific striatal interneuron types Support Protocol 2: Generation of ATAC-seq libraries from the nuclei of specific striatal neuron types Basic Protocol 4: Extraction of genomic DNA and nuclear RNA and preparation of sequencing libraries Basic Protocol 5: Processing and quality control of FANS-seq and ATAC-seq data.
中枢神经系统的大多数病理状况对所有细胞类型的影响程度并不相同。因此,要描绘出疾病症状背后的分子事件,包括基因、表观遗传和转录变化,就依赖于将特定细胞类型与其他细胞类型区分开来进行特征描述的能力。我们已经开发出一种方法,用于从冷冻的死后纹状体和大脑皮质中收集特定细胞类型的核RNA和基因组DNA。这使得对特定细胞群体进行深度转录组分析,并对其基因组和表观遗传特性进行表征成为可能。该方法基于细胞核的纯化,然后对用核酸探针或与特定细胞类型中存在的靶标结合的抗体标记的细胞核进行荧光激活分选(FANS)。该方案详细描述了从人脑组织中分离和标记神经元和神经胶质细胞核的程序、提取RNA和基因组DNA可采取的步骤、将该程序与ATAC-seq相结合以获取染色质可及性信息的方法,以及评估细胞类型特异性RNA-seq和ATAC-seq数据集质量的计算方法。© 2024作者。由Wiley Periodicals LLC出版的《当前方案》。基本方案1:组织匀浆、通过超速离心分离细胞核并进行甲醛固定 基本方案2:基于抗体的特定新皮质神经元类型细胞核的标记和分离 支持方案1:从大脑皮质特定神经元类型的细胞核生成ATAC-seq文库 基本方案3:基于核酸杂交的特定纹状体投射神经元类型细胞核的标记和分离 替代方案1:特定纹状体中间神经元类型细胞核的标记和分离 支持方案2:从特定纹状体神经元类型的细胞核生成ATAC-seq文库 基本方案4:基因组DNA和核RNA的提取以及测序文库的制备 基本方案5:FANS-seq和ATAC-seq数据的处理和质量控制。