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一种新型超灵敏原位杂交方法,用于以细胞分辨率检测短序列和剪接变体。

A Novel Ultrasensitive In Situ Hybridization Approach to Detect Short Sequences and Splice Variants with Cellular Resolution.

机构信息

Section on Molecular Neurobiology, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Porter Neuroscience Research Center, Bldg. 35, Room 2C-1000, Bethesda, MD, 20892, USA.

Institute of Molecular Psychiatry, University Bonn, 53127, Bonn, Germany.

出版信息

Mol Neurobiol. 2018 Jul;55(7):6169-6181. doi: 10.1007/s12035-017-0834-6. Epub 2017 Dec 20.

Abstract

Investigating the expression of RNAs that differ by short or single nucleotide sequences at a single-cell level in tissue has been limited by the sensitivity and specificity of in situ hybridization (ISH) techniques. Detection of short isoform-specific sequences requires RNA isolation for PCR analysis-an approach that loses the regional and cell-type-specific distribution of isoforms. Having the capability to distinguish the differential expression of RNA variants in tissue is critical because alterations in mRNA splicing and editing, as well as coding single nucleotide polymorphisms, have been associated with numerous cancers, neurological and psychiatric disorders. Here we introduce a novel highly sensitive single-probe colorimetric/fluorescent ISH approach that targets short exon/exon RNA splice junctions using single-pair oligonucleotide probes (~ 50 bp). We use this approach to investigate, with single-cell resolution, the expression of four transcripts encoding the neuregulin (NRG) receptor ErbB4 that differ by alternative splicing of exons encoding two juxtamembrane (JMa/JMb) and two cytoplasmic (CYT-1/CYT-2) domains that alter receptor stability and signaling modes, respectively. By comparing ErbB4 hybridization on sections from wild-type and ErbB4 knockout mice (missing exon 2), we initially demonstrate that single-pair probes provide the sensitivity and specificity to visualize and quantify the differential expression of ErbB4 isoforms. Using cell-type-specific GFP reporter mice, we go on to demonstrate that expression of ErbB4 isoforms differs between neurons and oligodendrocytes, and that this differential expression of ErbB4 isoforms is evolutionarily conserved to humans. This single-pair probe ISH approach, known as BaseScope, could serve as an invaluable diagnostic tool to detect alternative spliced isoforms, and potentially single base polymorphisms, associated with disease.

摘要

在单细胞水平上研究组织中由于短核苷酸序列或单个核苷酸序列差异而表达的 RNA,受到原位杂交(ISH)技术的灵敏度和特异性的限制。检测短的同工型特异性序列需要进行 RNA 分离以进行 PCR 分析 - 这种方法会丢失同工型的区域和细胞类型特异性分布。能够区分组织中 RNA 变体的差异表达至关重要,因为 mRNA 剪接和编辑的改变以及编码单核苷酸多态性与许多癌症、神经和精神疾病有关。在这里,我们介绍了一种新颖的高度敏感的单探针比色/荧光 ISH 方法,该方法使用单对寡核苷酸探针(~50bp)针对短外显子/外显子 RNA 剪接连接点。我们使用这种方法以单细胞分辨率研究了四种编码神经调节蛋白(NRG)受体 ErbB4 的转录本的表达,这些转录本通过编码两个跨膜(JMa/JMb)和两个细胞质(CYT-1/CYT-2)结构域的外显子的选择性剪接而不同,分别改变受体的稳定性和信号转导方式。通过比较野生型和 ErbB4 敲除小鼠(缺失外显子 2)切片上的 ErbB4 杂交,我们最初证明单对探针提供了灵敏度和特异性,可以可视化和量化 ErbB4 同工型的差异表达。使用细胞类型特异性 GFP 报告小鼠,我们继续证明 ErbB4 同工型在神经元和少突胶质细胞之间的表达不同,并且这种 ErbB4 同工型的差异表达在进化上与人类保守。这种称为 BaseScope 的单对探针 ISH 方法可以作为一种非常有价值的诊断工具,用于检测与疾病相关的选择性剪接同工型,并且可能是单碱基多态性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/02a8/5994223/d502307e498a/12035_2017_834_Fig1_HTML.jpg

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