Brown Jill M, Buckle Veronica J
MRC Molecular Haematology Unit, John Radcliffe Hospital, Weatherall Institute of Molecular Medicine, Headington, Oxford, UK.
Methods Mol Biol. 2010;659:33-50. doi: 10.1007/978-1-60761-789-1_3.
The development of cellular diversity within any organism depends on the timely and correct expression of differing subsets of genes within each tissue type. Many techniques exist which allow a global, average analysis of RNA expression; however, RNA-FISH permits the sensitive detection of specific transcripts within individual cells while preserving the cellular morphology. The technique can provide insight into the spatial and temporal organization of gene transcription as well the relationship of gene expression and mature RNA distribution to nuclear and cellular compartments. It can also reveal the intercellular variation of gene expression within a given tissue. Here, we describe RNA-FISH methodologies that allow the detection of nascent transcripts within the cell nucleus as well as protocols that allow the detection of RNA alongside DNA or proteins. Such techniques allow the placing of gene transcription within a functional context of the whole cell.
任何生物体中细胞多样性的发展取决于每种组织类型中不同基因子集的及时和正确表达。存在许多技术可对RNA表达进行全局平均分析;然而,RNA荧光原位杂交(RNA-FISH)能够在保留细胞形态的同时灵敏地检测单个细胞内的特定转录本。该技术可以深入了解基因转录的时空组织,以及基因表达和成熟RNA分布与细胞核和细胞区室的关系。它还可以揭示给定组织内基因表达的细胞间差异。在这里,我们描述了能够检测细胞核内新生转录本的RNA-FISH方法,以及能够同时检测RNA与DNA或蛋白质的实验方案。这些技术能够将基因转录置于整个细胞的功能背景中。