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使用双标记嵌合分析(MADM)在转录组水平探究突变体表型的细胞类型特异性。

Probing Cell-Type Specificity of Mutant Phenotype at Transcriptomic Level Using Mosaic Analysis with Double Markers (MADM).

作者信息

Cheung Giselle, Pauler Florian M, Hippenmeyer Simon

机构信息

Institute of Science and Technology Austria (ISTA), Klosterneuburg, Austria.

出版信息

Methods Mol Biol. 2025;2886:139-151. doi: 10.1007/978-1-0716-4310-5_7.

Abstract

Mosaic Analysis with Double Markers (MADM) represents a mouse genetic approach coupling differential fluorescent labeling to genetic manipulations in dividing cells and their lineages. MADM uniquely enables the generation and visualization of individual control or homozygous mutant cells in a heterozygous genetic environment. Among its diverse applications, MADM has been used to dissect cell-autonomous gene functions important for cortical development and neural development in general. The high cellular resolution offered by MADM also permits the analysis of transcriptomic changes of individual cells upon genetic manipulations. In this chapter, we describe an experimental protocol combining the generation and isolation of MADM-labeled cells with downstream single-cell RNA-sequencing technologies to probe cell-type specific phenotypes due to genetic mutations at single-cell resolution.

摘要

双标记镶嵌分析(MADM)是一种小鼠遗传学方法,它将差异荧光标记与分裂细胞及其谱系中的基因操作相结合。MADM独特地能够在杂合遗传环境中产生并可视化单个对照细胞或纯合突变细胞。在其多种应用中,MADM已被用于剖析对皮质发育和一般神经发育重要的细胞自主基因功能。MADM提供的高细胞分辨率还允许分析基因操作后单个细胞的转录组变化。在本章中,我们描述了一种实验方案,该方案将MADM标记细胞的产生和分离与下游单细胞RNA测序技术相结合,以在单细胞分辨率下探究由于基因突变导致的细胞类型特异性表型。

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