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使用RNA原位杂交分析法对小鼠脑切片中可变前体mRNA剪接进行定量分析。

Quantitative Analysis of Alternative Pre-mRNA Splicing in Mouse Brain Sections Using RNA In Situ Hybridization Assay.

作者信息

Guo Xuan, Zhao Yiqing, Nguyen Hieu, Liu Tonghua, Wang Zhenghe, Lou Hua

机构信息

Department of Genetics and Genome Sciences, Case Western Reserve University; Department of Endocrinology, Dongfang Hospital of Beijing University of Chinese Medicine.

Department of Genetics and Genome Sciences, Case Western Reserve University; Case Comprehensive Cancer Center, Case Western Reserve University.

出版信息

J Vis Exp. 2018 Aug 26(138):57889. doi: 10.3791/57889.

Abstract

Alternative splicing (AS) occurs in more than 90% of human genes. The expression pattern of an alternatively spliced exon is often regulated in a cell type-specific fashion. AS expression patterns are typically analyzed by RT-PCR and RNA-seq using RNA samples isolated from a population of cells. In situ examination of AS expression patterns for a particular biological structure can be carried out by RNA in situ hybridization (ISH) using exon-specific probes. However, this particular use of ISH has been limited because alternative exons are generally too short to design exon-specific probes. In this report, the use of BaseScope, a recently developed technology that employs short antisense oligonucleotides in RNA ISH, is described to analyze AS expression patterns in mouse brain sections. Exon 23a of neurofibromatosis type 1 (Nf1) is used as an example to illustrate that short exon-exon junction probes exhibit robust hybridization signals with high specificity in RNA ISH analysis on mouse brain sections. More importantly, signals detected with exon inclusion- and skipping-specific probes can be used to reliably calculate the percent spliced in values of Nf1 exon 23a expression in different anatomical areas of a mouse brain. The experimental protocol and calculation method for AS analysis are presented. The results indicate that BaseScope provides a powerful new tool to assess AS expression patterns in situ.

摘要

可变剪接(AS)发生在超过90%的人类基因中。可变剪接外显子的表达模式通常以细胞类型特异性方式受到调控。AS表达模式通常通过使用从细胞群体中分离的RNA样本进行逆转录聚合酶链反应(RT-PCR)和RNA测序来分析。使用外显子特异性探针通过RNA原位杂交(ISH)可以对特定生物结构的AS表达模式进行原位检测。然而,ISH的这种特殊用途受到了限制,因为可变外显子通常太短,无法设计外显子特异性探针。在本报告中,描述了使用BaseScope(一种最近开发的在RNA ISH中使用短反义寡核苷酸的技术)来分析小鼠脑切片中的AS表达模式。以1型神经纤维瘤病(Nf1)的外显子23a为例,说明短外显子-外显子连接探针在小鼠脑切片的RNA ISH分析中表现出具有高特异性的强大杂交信号。更重要的是,用外显子包含和跳跃特异性探针检测到的信号可用于可靠地计算小鼠脑不同解剖区域中Nf1外显子23a表达的剪接百分比值。本文介绍了AS分析的实验方案和计算方法。结果表明,BaseScope提供了一种强大的新工具来原位评估AS表达模式。

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